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24 pages, 1233 KiB  
Article
A Novel Feature Selection Strategy Based on the Harris Hawks Optimization Algorithm for the Diagnosis of Cervical Cancer
by Minhui Dong, Yu Wang, Yuki Todo and Yuxiao Hua
Electronics 2024, 13(13), 2554; https://doi.org/10.3390/electronics13132554 - 28 Jun 2024
Viewed by 470
Abstract
Cervical cancer is the fourth most commonly diagnosed cancer and one of the leading causes of cancer-related deaths among females worldwide. Early diagnosis can greatly increase the cure rate for cervical cancer. However, due to the need for substantial medical resources, it is [...] Read more.
Cervical cancer is the fourth most commonly diagnosed cancer and one of the leading causes of cancer-related deaths among females worldwide. Early diagnosis can greatly increase the cure rate for cervical cancer. However, due to the need for substantial medical resources, it is difficult to implement in some areas. With the development of machine learning, utilizing machine learning to automatically diagnose cervical cancer has currently become one of the main research directions in the field. Such an approach typically involves a large number of features. However, a portion of these features is redundant or irrelevant. The task of eliminating redundant or irrelevant features from the entire feature set is known as feature selection (FS). Feature selection methods can roughly be divided into three types, including filter-based methods, wrapper-based methods, and embedded-based methods. Among them, wrapper-based methods are currently the most commonly used approach, and many researchers have demonstrated that these methods can reduce the number of features while improving the accuracy of diagnosis. However, this method still has some issues. Wrapper-based methods typically use heuristic algorithms for FS, which can result in significant computational time. On the other hand, heuristic algorithms are often sensitive to parameters, leading to instability in performance. To overcome this challenge, a novel wrapper-based method named the Binary Harris Hawks Optimization (BHHO) algorithm is proposed in this paper. Compared to other wrapper-based methods, the BHHO has fewer hyper-parameters, which contributes to better stability. Furthermore, we have introduced a rank-based selection mechanism into the algorithm, which endows BHHO with enhanced optimization capabilities and greater generalizability. To comprehensively evaluate the performance of the proposed BHHO, we conducted a series of experiments. The experimental results show that the proposed BHHO demonstrates better accuracy and stability compared to other common wrapper-based FS methods on the cervical cancer dataset. Additionally, even on other disease datasets, the proposed algorithm still provides competitive results, proving its generalizability. Full article
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<p>The schematic diagram of the HHO algorithm.</p>
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<p>The examples of operations in the exploration phase.</p>
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<p>The examples of operations of soft actions.</p>
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<p>The examples of hard besiege.</p>
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<p>The examples of hard besiege with rapid dives.</p>
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<p>Flowchart of the experimental framework.</p>
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<p>Bar chart for the results of the cervical cancer dataset. Each bar denotes the best result under the feature selection method. There is a specific numerical value along with the classifier’s name at the top of each bar.</p>
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<p>Bar chart for the results of the Cleveland dataset. Each bar denotes the best result under the feature selection method. There is a specific numerical value along with the classifier’s name at the top of each bar.</p>
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<p>Bar chart for the results of the Z-Alizadeh Sani dataset. Each bar denotes the best result under the feature selection method. There is a specific numerical value along with the classifier’s name at the top of each bar.</p>
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<p>Bar chart for the results of the Parkinson dataset. Each bar denotes the best result under the feature selection method. There is a specific numerical value along with the classifier’s name at the top of each bar.</p>
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16 pages, 4094 KiB  
Article
Curdepsidone A Induces Intrinsic Apoptosis and Inhibits Protective Autophagy via the ROS/PI3K/AKT Signaling Pathway in HeLa Cells
by Sunjie Xu, Zhimin Li, Xiujuan Xin and Faliang An
Mar. Drugs 2024, 22(5), 227; https://doi.org/10.3390/md22050227 - 17 May 2024
Viewed by 1071
Abstract
Among female oncology patients, cervical cancer stands as the fourth most prevalent malignancy, exerting significant impacts on their health. Over 600,000 women received the diagnosis of cervical cancer in 2020, and the illness claimed over 300,000 lives globally. Curdepsidone A, a derivative of [...] Read more.
Among female oncology patients, cervical cancer stands as the fourth most prevalent malignancy, exerting significant impacts on their health. Over 600,000 women received the diagnosis of cervical cancer in 2020, and the illness claimed over 300,000 lives globally. Curdepsidone A, a derivative of depsidone, was isolated from the secondary metabolites of Curvularia sp. IFB-Z10. In this study, we revised the molecular structure of curdepsidone A and investigated the fundamental mechanism of the anti-tumor activity of curdepsidone A in HeLa cells for the first time. The results demonstrated that curdepsidone A caused G0/G1 phase arrest, triggered apoptosis via a mitochondrial apoptotic pathway, blocked the autophagic flux, suppressed the PI3K/AKT pathway, and increased the accumulation of reactive oxygen species (ROS) in HeLa cells. Furthermore, the PI3K inhibitor (LY294002) promoted apoptosis induced by curdepsidone A, while the PI3K agonist (IGF-1) eliminated such an effect. ROS scavenger (NAC) reduced curdepsidone A-induced cell apoptosis and the suppression of autophagy and the PI3K/AKT pathway. In conclusion, our results revealed that curdepsidone A hindered cell growth by causing cell cycle arrest, and promoted cell apoptosis by inhibiting autophagy and the ROS-mediated PI3K/AKT pathway. This study provides a molecular basis for the development of curdepsidone A as a new chemotherapy drug for cervical cancer. Full article
(This article belongs to the Special Issue Marine Bioactive Compound Discovery through OSMAC Approach)
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<p>Revision of the molecular structure of curdepsidone A (CDA). (<b>A</b>) The molecular structure of curdepsidone A. (<b>B</b>) The plot of linear correlation between the calculated and actual values for the <sup>13</sup>C of curdepsidone A. (<b>C</b>) Relative error analysis performed to assess the deviation between the calculated and actual <sup>13</sup>C values. (<b>D</b>) DP4 probability analysis was employed to evaluate the confidence level associated with the assignment of <sup>13</sup>C values for curdepsidone A.</p>
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<p>Curdepsidone A inhibited cell viability and induced G0/G1 phase arrest in HeLa cells. (<b>A</b>) HeLa cells were exposed to curdepsidone A at various concentrations for 24, 48, or 72 h. The cytotoxic activity of curdepsidone A in HeLa cell lines was measured. (<b>B</b>) HeLa cells were exposed to curdepsidone A for 24 h and stained with Hoechst 33342. DNA synthesis in HeLa cells was detected using an EdU assay. (<b>C</b>) HeLa cells were exposed to curdepsidone A for 24 h. The cell cycle in HeLa cells was analyzed. (<b>D</b>) The effects of curdepsidone A on the expression of the cell-cycle-related proteins CDK4, Cyclin D1, p27, and p21 at concentrations of 0, 1, 2, and 4 μM were examined. Values are mean ± SD, <span class="html-italic">n</span> = 3, * <span class="html-italic">p</span> &lt; 0.05. ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Curdepsidone A induced apoptosis of HeLa cells. (<b>A</b>) HeLa cells were exposed to curdepsidone A for 24 or 48 h. The effect of curdepsidone A on the apoptosis of HeLa cells was measured. (<b>B</b>) The effects of curdepsidone A on the expression of the apoptosis-related proteins caspase3, cl-caspase3, caspase7, cl-caspase7, PARP, and cl-PARP were examined. (<b>C</b>) Mitochondrial membrane potential (MMP) in HeLa cells treated with curdepsidone A for 48 h was analyzed. (<b>D</b>) The effects of curdepsidone A on the expression of the endogenous apoptosis-related proteins Bax, Bcl-2, Cyto-C (cytosol), Apaf-1, caspase9, and cl-caspase9 were examined. (<b>E</b>–<b>G</b>) HeLa cells were pretreated with Z-VAD-FMK (20 μM) for 2 h and then treated with curdepsidone A (10 μM) for 48 h. The apoptosis of HeLa cells (<b>E</b>), the cell viability (<b>F</b>), and the expression of caspase3, cl-caspase3, caspase7, cl-caspase7, PARP, and cl-PARP (<b>G</b>) were examined. Values are mean ± SD, <span class="html-italic">n</span> = 3, * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 versus the control group; <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 versus the CDA group.</p>
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<p>Curdepsidone A inhibited protective autophagy in HeLa cells. (<b>A</b>) HeLa cells were exposed to curdepsidone A for 48 h. The expression of autophagy-related proteins was examined. (<b>B</b>) The autophagy flux was detected using GFP-RFP-LC3B double-labeled adenovirus. (<b>C</b>,<b>D</b>) HeLa cells were treated with curdepsidone A (10 μM) alone or in combination with CQ (10 μM) for 48 h. The apoptosis of HeLa cells (<b>C</b>) and the expression of LC3, p62, caspase7, cl-caspase7, PARP, and cl-PARP (<b>D</b>) were examined. Values are mean ± standard deviation, <span class="html-italic">n</span> = 3, * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 versus the control group; <span class="html-italic"><sup>#</sup> p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 versus the CDA group.</p>
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<p>Curdepsidone A suppressed the PI3K/AKT pathway in HeLa cells. (<b>A</b>) HeLa cells were exposed to curdepsidone A for 48 h. The expression of PI3K/AKT pathway-related proteins was examined. (<b>B</b>–<b>D</b>) HeLa cells were pretreated with IGF-1 (200 ng/mL) or LY294002 (5 μM) for 2 h and then treated with curdepsidone A (10 μM) for 48 h. The apoptosis of HeLa cells (<b>B</b>) and the expression of caspase3, cl-caspase3, caspase7, cl-caspase7, PARP, and cl-PARP (<b>C</b>,<b>D</b>) were examined. Values are mean ± SD, <span class="html-italic">n</span> = 3, * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 versus the control group; <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 versus the CDA group.</p>
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<p>Curdepsidone A increased reactive oxygen species (ROS) generation in HeLa cells. (<b>A</b>) HeLa cells were exposed to curdepsidone A at concentrations of 0, 4, 6, and 8 μM for 24 h. Intracellular ROS levels were assessed. (<b>B</b>–<b>F</b>) HeLa cells were pretreated with NAC (5 mM) for 2 h and then treated with curdepsidone A (8 μM) for 24 h. Intracellular ROS levels (<b>B</b>), the apoptosis of HeLa cells (<b>C</b>), and the expression of caspase3, cl-caspase3, caspase7, cl-caspase7, PARP, cl-PARP (<b>D</b>), PI3K, AKT, p-AKT, mTOR, p-mTOR, Beclin-1, LC3 and p62 (<b>F</b>) were examined. Values are mean ± SD, <span class="html-italic">n</span> = 3, * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 versus the control group; <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 versus the CDA group.</p>
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<p>Curdepsidone A inhibited the growth of Hela cells.</p>
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16 pages, 269 KiB  
Article
Selecting and Tailoring Implementation Strategies to Improve Human Papillomavirus Vaccine Uptake in Zambia: A Nominal Group Technique Approach
by Mwansa Ketty Lubeya, Mulindi Mwanahamuntu, Carla J. Chibwesha, Moses Mukosha and Mary Kawonga
Vaccines 2024, 12(5), 542; https://doi.org/10.3390/vaccines12050542 - 15 May 2024
Viewed by 940
Abstract
The human papillomavirus (HPV) vaccine is effective in cervical cancer prevention. However, many barriers to uptake exist and strategies to overcome them are needed. Therefore, this study aimed to select and tailor implementation strategies to barriers identified by multiple stakeholders in Zambia. The [...] Read more.
The human papillomavirus (HPV) vaccine is effective in cervical cancer prevention. However, many barriers to uptake exist and strategies to overcome them are needed. Therefore, this study aimed to select and tailor implementation strategies to barriers identified by multiple stakeholders in Zambia. The study was conducted in Lusaka district between January and February 2023. Participants were purposively sampled from three stakeholder groups namely, adolescent girls, parents, and teachers and healthcare workers. With each of the stakeholders’ groups (10–13 participants per group), we used the nominal group technique to gain consensus to tailor feasible and acceptable implementation strategies for mitigating the identified contextual barriers. The identified barriers included low levels of knowledge and awareness about the HPV vaccine, being out of school, poor community sensitisation, lack of parental consent to vaccinate daughters, and myths and misinformation about the HPV vaccine. The lack of knowledge and awareness of the HPV vaccine was a common barrier across the three groups. Tailored strategies included conducting educational meetings and consensus-building meetings, using mass media, changing service sites, re-examining implementation, and involving patients/consumers and their relatives. Our study contributes to the available evidence on the process of selecting and tailoring implementation strategies to overcome contextual barriers. Policymakers should consider these tailored strategies to mitigate barriers and improve HPV vaccine uptake. Full article
(This article belongs to the Special Issue Vaccine Strategies for HPV-Related Cancers)
14 pages, 1448 KiB  
Article
Human Papilloma Virus Vaccination and Cervical Screening in the Italian Regions: An Overview of the Current State of the Art
by Angela Bechini, Claudia Cosma, Giulia Di Pisa, Alice Fanfani, Giulia Ionita, Davide Liedl, Carla Lunetta, Linda Martorella, Silvia Mele, Lorenzo Stacchini, Gabriele Vaccaro, Ornella Zuccaro, Stefano Valente, Gian Marco Prandi, Paolo Bonanni and Sara Boccalini
Vaccines 2024, 12(5), 504; https://doi.org/10.3390/vaccines12050504 - 7 May 2024
Viewed by 1083
Abstract
Human Papilloma Virus (HPV) infection and HPV-related cancers can be prevented through vaccinations and mass cervical screening programmes. The Ministry of Health in Italy provides recommendations on primary and secondary prevention of HPV-related diseases, but the 19 Italian regions and 2 autonomous provinces [...] Read more.
Human Papilloma Virus (HPV) infection and HPV-related cancers can be prevented through vaccinations and mass cervical screening programmes. The Ministry of Health in Italy provides recommendations on primary and secondary prevention of HPV-related diseases, but the 19 Italian regions and 2 autonomous provinces have organisational and decision-making autonomy, with differences in the strategies for offering prevention. The aim of this study is to describe the HPV vaccination and cervical screening offered in all Italian regions. Regional official documents up until 31 December 2021 were first identified. Subsequently, primary and secondary prevention experts from each region were interviewed to validate the previously collected data. The National Immunisation Plan (NIP) 2017–2019 recommends HPV vaccination from the age of 11 for both sexes, with a coverage target of 95%. HPV vaccination is offered free of charge or co-payment. All regions have screening programmes for cervical cancer, using PAP or HPV-DNA tests every three to five years. All regions have an electronic registry for vaccination and screening status. All regions have developed awareness-raising campaigns. It is important to harmonise regional policies with the implementation of information systems integration. The collected data could enhance both regional and national public health initiatives, bolstering the resilience of vaccination programs. Full article
(This article belongs to the Special Issue Vaccine Strategies for HPV-Related Cancers)
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<p>Adherence to the validation phase of the study (light grey: experts validated data for primary prevention and secondary prevention; grey: experts validated data for primary prevention or secondary prevention; black: experts did not validate any data).</p>
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<p>Range of ages of free-of-charge offer and co-payment of HPV vaccines for F (females) and M (males) without risk factors.</p>
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<p>HPV primary prevention for certain subpopulations based on risk factors by region (active or inactive vaccination is free of charge).</p>
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<p>HPV secondary prevention strategy by age in Italian regions.</p>
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17 pages, 2236 KiB  
Article
Human Papillomavirus Vaccination Acceleration and Introduction in Sub-Saharan Africa: A Multi-Country Cohort Analysis
by Gbadebo Collins Adeyanju, Tene-Alima Essoh, Annick Raissa Sidibe, Furaha Kyesi and Muyi Aina
Vaccines 2024, 12(5), 489; https://doi.org/10.3390/vaccines12050489 - 1 May 2024
Viewed by 1747
Abstract
Background: Cervical cancer, caused by human papillomavirus (HPV) infection, is the second-largest cancer killer of women in low- and middle-income countries. The brunt of the global burden is borne predominantly in Sub-Saharan Africa. In 2020 alone, 70,000 of the 100,000 infected women in [...] Read more.
Background: Cervical cancer, caused by human papillomavirus (HPV) infection, is the second-largest cancer killer of women in low- and middle-income countries. The brunt of the global burden is borne predominantly in Sub-Saharan Africa. In 2020 alone, 70,000 of the 100,000 infected women in Africa died from it, thereby making up 21% of global cervical cancer mortality. The introduction of the HPV vaccine into the National Immunization Program was expected to change the trajectory. However, uptake of the vaccination has been poor, especially for the second dose. Only about half of the countries in Africa currently provide the vaccine. Without urgent intervention, the 2030 global cervical cancer elimination targets will be undermined. The study aims to understand the key challenges facing the HPV vaccine and to develop a roadmap to accelerate the uptake. Method: Fourteen countries were purposively included using a cohort design methodology and the investigation spanned March–July 2023. The Africa region was stratified into three focus-group discussion cohorts (Abidjan, Nairobi and Dar es Salaam), comprising pre-selected countries that have already and those about to introduce the HPV vaccine. In each country, the EPI manager, the NITAG chair or representatives and an HPV-focal researcher were selected participants. The methods involved a collaborative and knowledge-sharing format through regional and country-specific discussions, plenary discussions, and workshop-style group missions. Results: The study reached a total of 78 key stakeholders, comprising 30 participants in cohort one, 21 in cohort two and 27 in cohort three. Key outcomes included the prevalence of declining HPV2 vaccination across all countries in the region; country-specific barriers impeding uptake were identified and strategy for accelerating vaccination demand initiated, e.g., utilizing investments from COVID-19 (e.g., electronic registry and multisector coordination); individual countries developing their respective HPV vaccination recovery and acceleration roadmaps; the identification and inclusion of a zero-dose catch-up strategy into the vaccination roadmaps; support for a transition from multiple-doses to a single-dose HPV vaccine; the incorporation of implementation science research to support the decision-making process such as vaccine choices, doses and understanding behavior. Conclusion: Beyond research, the study shows the significance of scientific approaches that are not limited to understanding problems, but are also solution-oriented, e.g., development of roadmaps to overcome barriers against HPV vaccination uptake. Full article
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<p>Population-adjusted coverage in Africa (2011–2021) [<a href="#B31-vaccines-12-00489" class="html-bibr">31</a>].</p>
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<p>Focus-group discussion cohorts.</p>
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<p>DoRIS study efficacy of single-dose versus multiple doses [<a href="#B29-vaccines-12-00489" class="html-bibr">29</a>].</p>
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<p>HPV Vaccination acceleration roadmap template.</p>
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<p>Strategies to foster HPV vaccine uptake.</p>
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16 pages, 8455 KiB  
Article
Immunoinformatics Design and In Vivo Immunogenicity Evaluation of a Conserved CTL Multi-Epitope Vaccine Targeting HPV16 E5, E6, and E7 Proteins
by Ni Guo, Zhixin Niu, Zhiling Yan, Weipeng Liu, Lei Shi, Chuanyin Li, Yufeng Yao and Li Shi
Vaccines 2024, 12(4), 392; https://doi.org/10.3390/vaccines12040392 - 9 Apr 2024
Viewed by 1302
Abstract
Human papillomavirus type 16 (HPV16) infection is responsible for more than 50% of global cervical cancer cases. The development of a vaccine based on cytotoxic T-lymphocyte (CTL) epitopes is a promising strategy for eliminating pre-existing HPV infections and treating patients with cervical cancer. [...] Read more.
Human papillomavirus type 16 (HPV16) infection is responsible for more than 50% of global cervical cancer cases. The development of a vaccine based on cytotoxic T-lymphocyte (CTL) epitopes is a promising strategy for eliminating pre-existing HPV infections and treating patients with cervical cancer. In this study, an immunoinformatics approach was used to predict HLA-I-restricted CTL epitopes in HPV16 E5, E6, and E7 proteins, and a set of conserved CTL epitopes co-restricted by human/murine MHCs was screened and characterized, with the set containing three E5, four E6, and four E7 epitopes. Subsequently, the immunogenicity of the epitope combination was assessed in mice, and the anti-tumor effects of the multi-epitope peptide vaccine E5E6E7pep11 and the recombinant protein vaccine CTB-Epi11E567 were evaluated in the TC-1 mouse tumor model. The results demonstrated that mixed epitope peptides could induce antigen-specific IFN-γ secretion in mice. Prophylactic immunization with E5E6E7pep11 and CTB-Epi11E567 was found to provide 100% protection against tumor growth in mice. Moreover, both types of the multi-epitope vaccine significantly inhibited tumor growth and prolonged mouse survival. In conclusion, in this study, a multi-epitope vaccine targeting HPV16 E5, E6, and E7 proteins was successfully designed and evaluated, demonstrating potential immunogenicity and anti-tumor effects and providing a promising strategy for immunotherapy against HPV-associated tumors. Full article
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<p>Flowchart and brief results of epitope prediction and screening in the present study.</p>
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<p>CTL/CD8<sup>+</sup> candidate epitope location maps plotted for the E5, E6, and E7 proteins.</p>
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<p>Induction of antigen-specific IFN-γ response in C57BL/6 mice vaccinated with E5E6E7pep11. C57BL/6 mice (<span class="html-italic">n</span> = 4) were inoculated intramuscularly (i.m.) with 100 μL of either PBS, CpG ODN 1826, or E5E6E7pep11 on days 0, 7, and 14. Splenic lymphocytes were collected 1 week after the second immunization process and then stimulated in vitro with the 11p-pool, E5-pool, E6-pool, and E7-pool. (<b>A</b>) The number of IFN-γ spot-forming cells (SFCs) detected using ELISpot was subtracted from the SFCs stimulated by serum-free medium as a negative control. (<b>B</b>) Representative ELISpot images, using 11p-pool as a specific stimulus, PMA as a non-specific stimulus (positive control), and serum-free medium as a negative stimulus (negative control). **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Prophylactic anti-tumor immunity induced by multi-epitope vaccines. (<b>A</b>) The C57BL/6 mice (<span class="html-italic">n</span> = 6) were intramuscularly vaccinated (i.m.) with 100 μL of PBS, CpG ODN 1826 (20 μg), E5E6E7pep11 (5 μg/peptide and 20 μg CpG ODN 1826), or CTB-Epi11E567 (100 μg) at 7, 14, and 21 days prior to the 1 × 10<sup>5</sup> TC-1 cell challenge. (<b>B</b>) Percentage survival of each group of mice within 80 days of tumor challenge. The mice were euthanized when their tumor diameter reached ≥ 15 mm.</p>
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<p>Therapeutic anti-tumor immune effects induced by multi-epitope vaccines. (<b>A</b>) The C57BL/6 mice (n = 6) were intramuscularly vaccinated (i.m.) with 100 μL of PBS, pep11 (5 μg/peptide), E5E6E7pep11 (5 μg/peptide and 20 μg CpG ODN 1826), or CTB-Epi11E567 (100 μg) at 3, 10, and 17 days post-challenge of 1 × 10<sup>5</sup> TC-1 cells. (<b>B</b>) Tumor volume was measured biweekly, and the average tumor sizes for each group of mice were computed to graph the kinetics of tumor growth. (<b>C</b>) Percentage survival of each group of mice within 80 days of tumor challenge. **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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20 pages, 385 KiB  
Article
“A Huge Gap”: Health Care Provider Perspectives on Cancer Screening for Aboriginal and Torres Strait Islander People in the Northern Territory
by Emma V. Taylor, Sarah Dugdale, Christine M. Connors, Gail Garvey and Sandra C. Thompson
Int. J. Environ. Res. Public Health 2024, 21(2), 141; https://doi.org/10.3390/ijerph21020141 - 27 Jan 2024
Cited by 1 | Viewed by 2659
Abstract
Cancer is one of the leading causes of death for Aboriginal and Torres Strait Islander people in the Northern Territory (NT). Accessible and culturally appropriate cancer screening programs are a vital component in reducing the burden of cancer. Primary health care plays a [...] Read more.
Cancer is one of the leading causes of death for Aboriginal and Torres Strait Islander people in the Northern Territory (NT). Accessible and culturally appropriate cancer screening programs are a vital component in reducing the burden of cancer. Primary health care plays a pivotal role in facilitating the uptake of cancer screening in the NT, due to the significant challenges caused by large distances, limited resources, and cultural differences. This paper analyses health care provider perspectives and approaches to the provision of cancer screening to Aboriginal people in the NT that were collected as part of a larger study. Semi-structured interviews were conducted with 50 staff from 15 health services, including 8 regional, remote, and very remote primary health care (PHC) clinics, 3 hospitals, a cancer centre, and 3 cancer support services. Transcripts were thematically analysed. Cancer screening by remote and very remote PHC clinics in the NT is variable, with some staff seeing cancer screening as a “huge gap”, while others see it as lower priority compared to other conditions due to a lack of resourcing and the overwhelming burden of acute and chronic disease. Conversely, some clinics see screening as an area where they are performing well, with systematic screening, targeted programs, and high screening rates. There was a large variation in perceptions of the breast screening and cervical screening programs. However, participants universally reported that the bowel screening kit was complicated and not culturally appropriate for their Aboriginal patients, which led to low uptake. System-level improvements are required, including increased funding and resourcing for screening programs, and for PHC clinics in the NT. Being appropriately resourced would assist PHC clinics to incorporate a greater emphasis on cancer screening into adult health checks and would support PHCs to work with local communities to co-design targeted cancer screening programs and culturally relevant education activities. Addressing these issues are vital for NT PHC clinics to address the existing cancer screening gaps and achieving the Australian Government pledge to be the first nation in the world to eliminate cervical cancer as a public health problem by 2035. The implementation of the National Lung Cancer Screening Program in 2025 also presents an opportunity to deliver greater benefits to Aboriginal communities and reduce the cancer burden. Full article
(This article belongs to the Special Issue Second Edition: Cancer Health Disparities and Public Health)
15 pages, 6963 KiB  
Article
Chitosan-Functionalized Poly(β-Amino Ester) Hybrid System for Gene Delivery in Vaginal Mucosal Epithelial Cells
by Xueqin Gao, Dirong Dong, Chong Zhang, Yuxing Deng, Jiahui Ding, Shiqi Niu, Songwei Tan and Lili Sun
Pharmaceutics 2024, 16(1), 154; https://doi.org/10.3390/pharmaceutics16010154 - 22 Jan 2024
Cited by 1 | Viewed by 1531
Abstract
Gene therapy displays great promise in the treatment of cervical cancer. The occurrence of cervical cancer is highly related to persistent human papilloma virus (HPV) infection. The HPV oncogene can be cleaved via gene editing technology to eliminate carcinogenic elements. However, the successful [...] Read more.
Gene therapy displays great promise in the treatment of cervical cancer. The occurrence of cervical cancer is highly related to persistent human papilloma virus (HPV) infection. The HPV oncogene can be cleaved via gene editing technology to eliminate carcinogenic elements. However, the successful application of the gene therapy method depends on effective gene delivery into the vagina. To improve mucosal penetration and adhesion ability, quaternized chitosan was introduced into the poly(β-amino ester) (PBAE) gene-delivery system in the form of quaternized chitosan-g-PBAE (QCP). At a mass ratio of PBAE:QCP of 2:1, the polymers exhibited the highest green fluorescent protein (GFP) transfection efficiency in HEK293T and ME180 cells, which was 1.1 and 5.4 times higher than that of PEI 25 kD. At this mass ratio, PBAE–QCP effectively compressed the GFP into spherical polyplex nanoparticles (PQ–GFP NPs) with a diameter of 255.5 nm. In vivo results indicated that owing to the mucopenetration and adhesion capability of quaternized CS, the GFP transfection efficiency of the PBAE–QCP hybrid system was considerably higher than those of PBAE and PEI 25 kD in the vaginal epithelial cells of Sprague–Dawley rats. Furthermore, the new system demonstrated low toxicity and good safety, laying an effective foundation for its further application in gene therapy. Full article
(This article belongs to the Special Issue Delivery System for Biomacromolecule Drugs: Design and Application)
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<p>Synthesis and characterization of QCP. (<b>A</b>) Synthesis of QCP. (<b>B</b>) <sup>1</sup>H-NMR of QCP and intermediate products.</p>
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<p>Transfection efficiency of PQ–GFP NPs on HEK293T and ME180 cells. Bright field (gray, for cell localization) and fluorescent images, cytometric analysis of transfection efficiency, and relative number of viable cells (LCC) of PQ–GFP NPs transfected HEK293T cells (<b>A</b>–<b>C</b>) and ME180 cells (<b>D</b>–<b>F</b>) at different mass ratios of PBAE and QCP for 36 h. Scale bar, 100 μm.</p>
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<p>Bright field (gray, for cell localization), fluorescence images, and cytometric analysis of transfection efficiency of PQ–GFP NPs on HEK293T (<b>A</b>) and ME180 (<b>B</b>) cells at different mass ratios of PQ and GFP for 36 h with a mass ratio of PBAE and QCP of 2:1. Scale bar, 100 μm.</p>
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<p>Characterization of PQ–GFP NPs. (<b>A</b>) Particle size and ζ-potential of PQ–GFP NPs. (<b>B</b>) Stability of PQ–GFP NPs in FBS at room temperature. (<b>C</b>) TEM image of PQ–GFP NPs. Scale bar, 300 nm. (<b>D</b>) Agarose gel electrophoresis pattern at different mass ratios of material and GFP with or without heparin. (<b>E</b>) Cytotoxicity of PQ–GFP NPs on ME180 cells. (<b>F</b>) Mucoadhesion rates of PBAE–Ce6/QCP–GFP NPs in the vagina of SD rats. Each point represents the mean ± SD (n = 3). One-way ANOVA was used for statistical analysis, **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Transfection of PQ–GFP and PEI–GFP NPs in SiHa and HeLa cell lines. Scale bar, 100 μm.</p>
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<p>The in vivo transfection effect in SD rat vagina. (<b>A</b>) Fluorescence images and (<b>B</b>) flow cytometry analysis of the vaginal/cervix epithelial cells of SD rats treated with PEI, PBAE, QCP, and PQ–GFP NPs. Scale bars, 100 μm. (<b>C</b>) Frozen section images of SD rat vagina treated with different groups. Cervical/vaginal mucosa are marked by red circles. Scale bars, 200 μm.</p>
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<p>Toxicity analysis of PEI, PBAE, and PQ–GFP NPs in SD rats. (<b>A</b>) Routine blood and (<b>B</b>) blood biochemical tests of toxicity experiment for each group. Quantitative analysis of WBC, RBC, HGB, MCV, MCH, PLT, ALT, AST, ALP, BUN, GLU, and CHO. Each point represents the mean ± SD (n = 3). (<b>C</b>) Representative images of H&amp;E staining of vagina and adjacent organs (cervix, uterus, ovary, urethra, rectum, and colon) in SD rats treated with PEI, PBAE, and PQ–GFP NPs. Scale bars, 100 μm. One-way ANOVA was used for statistical analysis; ns: no significant difference.</p>
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13 pages, 3475 KiB  
Article
Modeling the Health Impact and Cost-Effectiveness of a Combined Schoolgirl HPV Vaccination and Cervical Cancer Screening Program in Guangdong Province, China
by Yating Huang, Dantao Zhang, Lihua Yin, Jianguo Zhao, Zhifeng Li, Jing Lu, Xiaoming Zhang, Chenggang Wu and Wei Wu
Children 2024, 11(1), 103; https://doi.org/10.3390/children11010103 - 15 Jan 2024
Viewed by 1422
Abstract
Low human papillomavirus (HPV) vaccine uptake is a key barrier to cervical cancer elimination. We aimed to evaluate the health impact and cost-effectiveness of introducing different HPV vaccines into immunization programs and scaling up the screening program in Guangdong. We used a dynamic [...] Read more.
Low human papillomavirus (HPV) vaccine uptake is a key barrier to cervical cancer elimination. We aimed to evaluate the health impact and cost-effectiveness of introducing different HPV vaccines into immunization programs and scaling up the screening program in Guangdong. We used a dynamic compartmental model to estimate the impact of intervention strategies during 2023–2100. We implemented the incremental cost-effectiveness ratio (ICER) in costs per averted disability-adjusted life year (DALY) as an indicator to assess the effectiveness of the intervention. We used an age-standardized incidence of 4 cases per 100,000 women as the threshold for the elimination of cervical cancer. Compared with the status quo, scaling up cervical cancer screening coverage alone would prevent 215,000 (95% CI: 205,000 to 227,000) cervical cancer cases and 49,000 (95% CI: 48,000 to 52,000) deaths during 2023–2100. If the coverage of vaccination reached 90%, domestic two-dose 2vHPV vaccination would be more cost-effective than single-dose and two-dose 9vHPV vaccination. If Guangdong introduced domestic two-dose 2vHPV vaccination at 90% coverage for schoolgirls from 2023 and increased the screening coverage, cervical cancer would be eliminated by 2049 (95% CI 2047 to 2051). Introducing two doses of domestic 2vHPV vaccination for schoolgirls and expanding cervical cancer screening is estimated to be highly cost-effective to accelerate the elimination of cervical cancer in Guangdong. Full article
(This article belongs to the Section Pediatric Infectious Diseases)
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<p>Conditions versus model output after calibration. (<b>A</b>–<b>C</b>) represent the following variables: HPV prevalence (%), Crude cervical cancer incidence rate (/10<sup>5</sup>), Crude cervical cancer mortality rate (/10<sup>5</sup>); Red dot represents observed local epidemiological values, black dot indicates predicted values from the model.</p>
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<p>Projection of age-standardized incidence of cervical cancer with different strategies between 2023 and 2100. (<b>A</b>–<b>C</b>) at the current screening rate; (<b>D</b>–<b>F</b>) in the context of expanding cervical cancer screening.</p>
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<p>Tornado diagram for two-dose 2vHPV vaccination versus two-dose 9vHPV vaccination ICER in the context of expanding cervical cancer screening.</p>
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<p>Two-dimensional cost-effectiveness plane demonstrating the distribution of 1000 simulations: two-dose 2vHPV vaccination versus two-dose 9vHPV vaccination in the context of expanding cervical cancer screening at different (100%, 70%, 50%, 30%) price level.</p>
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12 pages, 1471 KiB  
Article
The Global Demand and Supply Balance of the Human Papillomavirus Vaccine: Implications for the Global Strategy for the Elimination of Cervical Cancer
by Stefano Malvolti, Adam Soble, Paul Bloem, D Scott LaMontagne, Rakesh Aggarwal, Punnee Pitisuttithum, Helen Rees and Tania Cernuschi
Vaccines 2024, 12(1), 4; https://doi.org/10.3390/vaccines12010004 - 19 Dec 2023
Cited by 1 | Viewed by 1935
Abstract
As of November 2023, 140 World Health Organization (WHO) member states had introduced human papillomavirus (HPV) vaccination in their routine immunization schedules. Despite a continuously increasing demand from countries across all income groups, supply constraints, COVID-19 pandemic disruptions, and other factors have slowed [...] Read more.
As of November 2023, 140 World Health Organization (WHO) member states had introduced human papillomavirus (HPV) vaccination in their routine immunization schedules. Despite a continuously increasing demand from countries across all income groups, supply constraints, COVID-19 pandemic disruptions, and other factors have slowed the pace of introduction, particularly in low-resource settings. Using a population-based forecasting methodology and leveraging the WHO’s yearly vaccine supply data collection, we updated global demand and supply projections for the HPV vaccine for the period of 2022–2031. The analysis aimed at clarifying the magnitude of the challenges to bringing in equitable access to HPV vaccines, which can hinder the achievement of the Global Strategy for the Elimination of Cervical Cancer. The results of this analysis show that the risk of HPV shortages has significantly decreased, and global supply is now, under normal circumstances, sufficient to meet global demand. In the long term, HPV supply will be more than sufficient to meet the Global Strategy’s goal of 90% of girls fully vaccinated with the HPV vaccine by the age of 15 years. Nonetheless, paying attention to the formulation of policies and carefully managing demand and supply will be required to ensure the long-term sustainability of the HPV vaccine program. Full article
(This article belongs to the Section Human Papillomavirus Vaccines)
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<p>HPV vaccine introduction status by country procurement group in 2021.</p>
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<p>Comparison of unconstrained demand scenarios.</p>
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<p>Available supply for commercialization forecast.</p>
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<p>Supply/demand balance.</p>
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<p>HPV self-procured price per dose (2021).</p>
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0 pages, 2496 KiB  
Article
Regulatory Effect of Ficus carica Latex on Cell Cycle Progression in Human Papillomavirus-Positive Cervical Cancer Cell Lines: Insights from Gene Expression Analysis
by Muharrem Okan Cakir, Ugur Bilge, Arshia Ghanbari and G. Hossein Ashrafi
Pharmaceuticals 2023, 16(12), 1723; https://doi.org/10.3390/ph16121723 - 12 Dec 2023
Viewed by 1460
Abstract
Cervical cancer presents a significant global health concern with high-risk human papillomaviruses (HPVs) identified as the main cause of this cancer. Although current treatment methods for cervical cancer can eliminate lesions, preventing metastatic spread and minimizing tissue damage remain a major challenge. Therefore, [...] Read more.
Cervical cancer presents a significant global health concern with high-risk human papillomaviruses (HPVs) identified as the main cause of this cancer. Although current treatment methods for cervical cancer can eliminate lesions, preventing metastatic spread and minimizing tissue damage remain a major challenge. Therefore, the development of a safer and innovative therapeutic approach is of the utmost importance. Natural products like fig latex, derived from the Ficus carica tree, have demonstrated promising anti-cancer properties when tested on cervical cancer cell lines. However, the specific mechanisms by which fig latex exerts its effects are still unknown. In this study, we conducted RNA-Seq analysis to explore how fig latex may counteract carcinogenesis in HPV-positive cervical cancer cell lines, namely, CaSki (HPV type 16-positive) and HeLa (HPV type 18-positive). Our results from this investigation indicate that fig latex influences the expression of genes associated with the development and progression of cervical cancer, including pathways related to “Nonsense-Mediated Decay (NMD)”, “Cell Cycle regulation”, “Transcriptional Regulation by TP53”, and “Apoptotic Process”. This selective impact of fig latex on cancer-related pathways suggests a potential novel therapeutic approach for HPV-related cervical cancer. Full article
(This article belongs to the Special Issue Exploring Natural Products with Antioxidant and Anticancer Properties)
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<p>The effect of whole fig latex on the growth of cervical cell lines. (<b>A</b>) HCKT1, (<b>B</b>) HeLa, and (<b>C</b>) CaSki were treated with different concentrations of whole fig latex (5 μg/mL, 10 μg/mL, 50 μg/mL, 100 μg/mL, and 200 μg/mL) for 72 h. The SRB assay was used to determine cell viability. Data points represent the mean ± SD of three independent experiments, each performed in triplicate. The IC50 values were calculated using R software (version 3.6.1) using a sigmoidal curve fit based on nonlinear regression. Statistical significance was assessed by one-way ANOVA followed by Tukey post hoc test and represented as follows: * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 vs. whole fig latex 0 μg/mL in DMSO. Doxorubicin was employed as the positive control in the SRB assay.</p>
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<p>The effect of fig latex on the cell cycle progression in human cervical cell lines. Different human cervical cancer cells, HeLa and CaSki, and normal healthy human cervical keratinocytes were incubated with 100 μg/mL of fig latex for 72 h. The representative cell cycle distribution of each cell type was analysed using flow cytometry. All experiments were conducted three times independently, each in triplicate.</p>
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<p>Complete upstream pathways that connect enriched transcription factors to kinases through known protein–protein interactions. Red nodes represent top transcription factors predicted to regulate the expression of the input gene list; grey nodes represent proteins that physically interact with the enriched transcription factors and connect them. Blue nodes represent the top predicted protein kinases known to phosphorylate the proteins within the expanded subnetwork. Green network edges/links represent kinase–substrate phosphorylation interactions between kinases and their substrates, while grey network edges represent physical protein–protein interactions.</p>
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20 pages, 8244 KiB  
Article
Deep Reinforcement Learning for Efficient Digital Pap Smear Analysis
by Carlos Macancela, Manuel Eugenio Morocho-Cayamcela and Oscar Chang
Computation 2023, 11(12), 252; https://doi.org/10.3390/computation11120252 - 10 Dec 2023
Viewed by 1861
Abstract
In August 2020, the World Health Assembly launched a global initiative to eliminate cervical cancer by 2030, setting three primary targets. One key goal is to achieve a 70% screening coverage rate for cervical cancer, primarily relying on the precise analysis of Papanicolaou [...] Read more.
In August 2020, the World Health Assembly launched a global initiative to eliminate cervical cancer by 2030, setting three primary targets. One key goal is to achieve a 70% screening coverage rate for cervical cancer, primarily relying on the precise analysis of Papanicolaou (Pap) or digital Pap smears. However, the responsibility of reviewing Pap smear samples to identify potentially cancerous cells primarily falls on pathologists—a task known to be exceptionally challenging and time-consuming. This paper proposes a solution to address the shortage of pathologists for cervical cancer screening. It leverages the OpenAI-GYM API to create a deep reinforcement learning environment utilizing liquid-based Pap smear images. By employing the Proximal Policy Optimization algorithm, autonomous agents navigate Pap smear images, identifying cells with the aid of rewards, penalties, and accumulated experiences. Furthermore, the use of a pre-trained convolutional neuronal network like Res-Net50 enhances the classification of detected cells based on their potential for malignancy. The ultimate goal of this study is to develop a highly efficient, automated Papanicolaou analysis system, ultimately reducing the need for human intervention in regions with limited pathologists. Full article
(This article belongs to the Special Issue 10th Anniversary of Computation—Computational Biology)
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<p>Conceptualization of the proposed approach.</p>
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<p>Pap smear samples: (<b>a</b>) Negative for intraepithelial lesion or malignancy (NILM). (<b>b</b>) Low-grade intraepithelial lesions (LSIL). (<b>c</b>) High-grade intraepithelial lesions (HSIL). (<b>d</b>) Squamous cell carcinoma (SCC).</p>
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<p>Examples of extracted “Cells”.</p>
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<p>Examples of extracted “No cells”.</p>
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<p>The figure illustrates a stack of frames, visually representing the environment in which an agent interacts. The agent is characterized by two black squares and the motion it exhibits within the frames.</p>
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<p>Graphical representation of two environments. (<b>A</b>) It is the environment where the agent searches for cells, and the captured image by the ROI is displayed in the right window. (<b>B</b>) The cells that have been detected.</p>
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<p>A visual depiction of how data moves through the CNN.</p>
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<p>Residual block architecture of ResNet model.</p>
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<p>Graphic representation of the stages during the training process.</p>
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<p>The left plot shows all the first set of agents’ mean rewards, permitting the ability to visually compare their training process. The right plot shows only three agents, agent D was not considered because it has the lowest values.</p>
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<p>The left plot shows all the second set of agents’ scores, permitting the ability to visually compare their training process. The right plot shows only three agents, agent H was not considered because it has the lowest values.</p>
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<p>The graph shows the retraining results of the agents C, E, and F.</p>
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<p>The graph shows the retraining results of the four extensively trained agents.</p>
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<p>The figure illustrates the behavior of an untrained agent. Red dots represent discovered cells, while the blue bar indicates repetitive visits to the same position.</p>
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<p>The figure shows three distinct environments utilized for testing the agents during the second and third stages of experiments.</p>
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<p>Tracking results of the agents E1, E2, E3, and E4 from the last stage in the first environment.</p>
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<p>Tracking results of the agents E1, E2, E3, and E4 from the last stage in the second environment.</p>
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<p>Tracking results of the agents E1, E2, E3, and E4 from the last stage in the third environment.</p>
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<p>ResNet-50 behavior in training and validation accuracy during 100 epochs.</p>
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<p>ResNet-50 behavior in training and validation loss during 100 epochs.</p>
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<p>The figure demonstrates three instances in which the agent successfully detects cells and accurately classifies them. The agent detected LSHL, HSIL, and SCC cells.</p>
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22 pages, 1156 KiB  
Article
Cervical Cancer Diagnosis Using Stacked Ensemble Model and Optimized Feature Selection: An Explainable Artificial Intelligence Approach
by Abdulaziz AlMohimeed, Hager Saleh, Sherif Mostafa, Redhwan M. A. Saad and Amira Samy Talaat
Computers 2023, 12(10), 200; https://doi.org/10.3390/computers12100200 - 7 Oct 2023
Cited by 4 | Viewed by 2122
Abstract
Cervical cancer affects more than half a million women worldwide each year and causes over 300,000 deaths. The main goals of this paper are to study the effect of applying feature selection methods with stacking models for the prediction of cervical cancer, propose [...] Read more.
Cervical cancer affects more than half a million women worldwide each year and causes over 300,000 deaths. The main goals of this paper are to study the effect of applying feature selection methods with stacking models for the prediction of cervical cancer, propose stacking ensemble learning that combines different models with meta-learners to predict cervical cancer, and explore the black-box of the stacking model with the best-optimized features using explainable artificial intelligence (XAI). A cervical cancer dataset from the machine learning repository (UCI) that is highly imbalanced and contains missing values is used. Therefore, SMOTE-Tomek was used to combine under-sampling and over-sampling to handle imbalanced data, and pre-processing steps are implemented to hold missing values. Bayesian optimization optimizes models and selects the best model architecture. Chi-square scores, recursive feature removal, and tree-based feature selection are three feature selection techniques that are applied to the dataset For determining the factors that are most crucial for predicting cervical cancer, the stacking model is extended to multiple levels: Level 1 (multiple base learners) and Level 2 (meta-learner). At Level 1, stacking (training and testing stacking) is employed for combining the output of multi-base models, while training stacking is used to train meta-learner models at level 2. Testing stacking is used to evaluate meta-learner models. The results showed that based on the selected features from recursive feature elimination (RFE), the stacking model has higher accuracy, precision, recall, f1-score, and AUC. Furthermore, To assure the efficiency, efficacy, and reliability of the produced model, local and global explanations are provided. Full article
(This article belongs to the Section Internet of Things (IoT) and Industrial IoT)
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<p>The main steps for predicting cervical cancer.</p>
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<p>Feature selection techniques.</p>
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<p>The proposed stacking model for predicting cervical cancer.</p>
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<p>Feature scores based on Chi2.</p>
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<p>Importance of selected features by based tree.</p>
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<p>The ranking of selected features according to RFE.</p>
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<p>ROC of REF chi2 models with selected features.</p>
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<p>ROC of REF for models with selected features.</p>
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<p>ROC of tree-based models with selected features.</p>
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<p>The best models.</p>
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<p>Global explanation of stacking model according to SHAP explainer.</p>
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<p>SHAP summary plot according to mean SHAP values.</p>
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<p>Force plot for specific instance. (<b>A</b>) instance with class 0, (<b>B</b>) instance with class 1.</p>
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15 pages, 1614 KiB  
Article
Accuracy of Human Papillomavirus (HPV) Testing on Urine and Vaginal Self-Samples Compared to Clinician-Collected Cervical Sample in Women Referred to Colposcopy
by Marianna Martinelli, Chiara Giubbi, Maria Letizia Di Meo, Federica Perdoni, Rosario Musumeci, Biagio Eugenio Leone, Robert Fruscio, Fabio Landoni and Clementina Elvezia Cocuzza
Viruses 2023, 15(9), 1889; https://doi.org/10.3390/v15091889 - 7 Sep 2023
Cited by 5 | Viewed by 2707
Abstract
In the context of cervical cancer prevention, where human papillomavirus (HPV) infection is pivotal, HPV testing is replacing Pap Smear in primary screening. This transition offers an opportunity for integrating self-sampling to enhance coverage. We evaluated the accuracy of HPV testing using self-collected [...] Read more.
In the context of cervical cancer prevention, where human papillomavirus (HPV) infection is pivotal, HPV testing is replacing Pap Smear in primary screening. This transition offers an opportunity for integrating self-sampling to enhance coverage. We evaluated the accuracy of HPV testing using self-collected urine and vaginal samples, comparing them to physician-collected cervical swabs. From a cohort of 245 women with abnormal cytology, we collected self-sampled vaginal, urine, and clinician-administered cervical specimens. Employing Anyplex™II HPV28 assay, outcomes revealed HPV positivity rates of 75.1% (cervical), 78.4% (vaginal), and 77.1% (urine). Significant, hr-HPV detection concordance was observed between self-taken cervical samples and clinical counterparts (k = 0.898 for vaginal; k = 0.715 for urine). This study extends beyond accuracy, highlighting self-collected sample efficacy in detecting high-grade cervical lesions. The insight underscores self-sampling’s role in bolstering participation and aligns with WHO’s goal to eliminate cervical cancer by 2030. Full article
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<p>hr-HPV DNA detection using the two different nucleic acid extraction protocols.</p>
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<p>Prevalence of different high-risk HPV genotypes.</p>
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<p>Prevalence of different low-risk HPV genotypes.</p>
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<p>Multiple hr-HPV infections in cervical, vaginal, and urine samples.</p>
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<p>hr-HPV-type-specific agreement between cervical and vaginal self-samples.</p>
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<p>hr-HPV-type-specific agreement between cervical and urine samples.</p>
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10 pages, 252 KiB  
Article
HPV Opportunistic Vaccination: A Literature Review and a Single-Center Experience in Northern Italy through the COVID-19 Pandemic
by Francesco Cantatore, Nadia Agrillo, Alessandro Camussi and Massimo Origoni
Vaccines 2023, 11(9), 1435; https://doi.org/10.3390/vaccines11091435 - 31 Aug 2023
Viewed by 1821
Abstract
The World Health Organization (WHO) set the goal of 90% HPV vaccination coverage in the population to eliminate cervical cancer. Opportunistic vaccination is performed outside the free vaccination or catch-up programs. Both free and opportunistic HPV vaccination programs experienced slowdowns during the COVID-19 [...] Read more.
The World Health Organization (WHO) set the goal of 90% HPV vaccination coverage in the population to eliminate cervical cancer. Opportunistic vaccination is performed outside the free vaccination or catch-up programs. Both free and opportunistic HPV vaccination programs experienced slowdowns during the COVID-19 pandemic. In this retrospective study, we aimed to identify the benefits and the obstacles of opportunistic vaccination among male and female individuals who took advantage of the “on-demand” service offered by San Raffaele Hospital in Milan from April 2018 to May 2023. The impact that the COVID-19 pandemic had on vaccination adherence was also analyzed. Data on a total of 527 subjects were collected from an in-house database and through personal interviews. Women in the cohort of older patients (over 25) adhered to the vaccination schedule more than younger women. Opportunistic vaccination request is influenced by the need of a gynecologist, a general practitioner, or public health clinic availability. Women also showed good adherence to screening, demonstrating awareness of the importance of cervical cancer secondary prevention despite vaccination. Opportunistic vaccination offers the possibility of including individuals excluded from the free vaccination campaigns, often already affected by lesions caused by HPV, providing increased viral clearance and faster lesion regression. The main limit remains the economic burden. Full article
(This article belongs to the Section Human Papillomavirus Vaccines)
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