Abstract
Most cancer cells primarily produce their energy through a high rate of glycolysis followed by lactic acid fermentation even in the presence of abundant oxygen. Pyruvate dehydrogenase kinase (PDK) 1, an enzyme responsible for aerobic glycolysis via phosphorylating and inactivating pyruvate dehydrogenase (PDH) complex, is commonly overexpressed in tumors and recognized as a therapeutic target in colorectal cancer. Hemistepsin A (HsA) is a sesquiterpene lactone isolated from Hemistepta lyrata Bunge (Compositae). Here, we report that HsA is a PDK1 inhibitor can reduce the growth of colorectal cancer and consequent activation of mitochondrial ROS-dependent apoptotic pathway both in vivo and in vitro. Computational simulation and biochemical assays showed that HsA directly binds to the lipoamide-binding site of PDK1, and subsequently inhibits the interaction of PDK1 with the E2 subunit of PDH complex. As a result of PDK1 inhibition, lactate production was decreased, but oxygen consumption was increased. Mitochondrial ROS levels and mitochondrial damage were also increased. Consistent with these observations, the apoptosis of colorectal cancer cells was promoted by HsA with enhanced activation of caspase-3 and -9. These results suggested that HsA might be a potential candidate for developing a novel anti-cancer drug through suppressing cancer metabolism.
Similar content being viewed by others
Introduction
Colorectal cancer (CRC) is the third most commonly diagnosed malignant cancer and the fourth leading cause of cancer-associated deaths in the world1. Cancer cells generate their energy through a high level of glycolysis, rather than relying on mitochondrial oxidative phosphorylation (OXPHOS) even in the presence of oxygen2,3. Although cancer is heterogeneous and many cancers have been found to rely on both glycolysis and OXPHOS4, upregulated glycolysis was reported as a prognostic factor of CRC5. Thus, targeting aerobic glycolysis, i.e. Warburg effect, is expected to be a promising strategy against CRC.
Four different isoforms of pyruvate dehydrogenase kinase (PDK) have been reported to be variably overexpressed in different types of cancer. The PDKs inactivate the pyruvate dehydrogenase (PDH) complex by phosphorylating its E1α subunit (PDHA1)6. Suppression of PDH by PDKs prevents the conversion of pyruvate into acetyl-CoA; instead, the pyruvate is converted into lactate7. PDK1, which phosphorylates all three sites of PDHA1 (S232, S293, and S300)8, is frequently overexpressed in cancer including gastric cancer, acute myeloid leukemia, non-small cell lung cancer, and CRC9,10,11,12. Previous studies have also shown that inhibition of PDK1 activity using a small molecule inhibitor can suppress the proliferation and growth of CRC11,12. Therefore, to regulate the Warburg effect, we focus on targeting pyruvate dehydrogenase kinase (PDK) 1. Previously, our group identified several novel PDK1 inhibitors, including Huzhangoside A isolated from Anemone rivularis and Ilimaquinone from Smenospongia cerebriformis13,14.
Hemistepsin A (HsA) is a sesquiterpene lactone isolated from Hemistepta lyrata Bunge which has been used for the treatment of colon diseases, such as diarrhea and anal fistula. HsA has been reported for its anti-tumor property against several tumor types15. However, the precise mechanism of the anti-tumor effect or the in vivo efficacy of HsA on CRC had not been explored. In this study, we demonstrated that HsA has an inhibitory effect on PDK1 activity, and it subsequently induces mitochondrial reactive oxygen species (ROS)-mediated apoptosis of CRC cells in both in vitro and in vivo studies.
Results
HsA shows cytotoxic effects on colorectal cancer cells in vitro
The chemical structure of HsA illustrated in Fig. 1A was already confirmed by nuclear magnetic resonance spectroscopy16. The in vitro cytotoxic effect of HsA was measured in several CRC cells, including SW480, HT29, RKO, DLD-1, and murine CT26. HsA showed significant cytotoxicity in the CRC cells at a concentration of 50 μM at 24 h time point. However, under the same conditions, HsA showed much lower cytotoxicity in normal human fibroblast Detroit 551 cells (Fig. 1B–G). We also calculated the IC50 of HsA assuming the concentration of HsA inhibits the growth of 50% of each cell line and found that DLD-1 cells were most sensitive to HsA among the human colon cancer cell lines (Table S2). Then, we observed the long-term effect of HsA in DLD-1 cells (Fig. 1H–I). HsA significantly reduced the number of surviving colonies of DLD-1 cells. Thus, the human DLD-1 colon adenocarcinoma cells were selected for further in vitro assays.
HsA suppresses lactate production and reduces the phosphorylation of PDHA1
The human colon cancer DLD-1 cells and murine colorectal cancer CT26 cells were treated with HsA for 4 h. HsA did not show any cytotoxic effect at a concentration of 10 μM in both DLD-1 and CT26 cells (Fig. S1). Thus, several in vitro assays were performed at the conditions. The amount of extracellular lactate was significantly decreased upon HsA treatment in a dose-dependent manner (Fig. 2A). To identify how HsA reduces lactate production, the activities and expressions of LDHA and PDKs, two major enzymes involved in converting pyruvate into lactate17, were examined. As shown in Fig. 2B–D HsA did not show a significant effect on in vitro and intracellular LDHA activity nor its expression. On the other hand, the HsA treatment markedly reduced the phosphorylation of PDHA1 in DLD-1 and CT 26 cells (Figs. 2E and S2). However, HsA did not affect the expression of the PDK isotypes, such as PDK1, PDK2, PDK3, and PDK4, in both cell lines. The expression of PDK3 was not detected in DLD-1 cells (data not shown). We tested whether HsA has an inhibitory effect on hypoxia-induced phosphorylation of PDHA1. As shown in Fig. 2F, hypoxia increased PDK1 and p-PDHA (S232, S293, and S300) expression. However, increased p-PDHA1 levels were decreased by HsA treatment. These results indicate that HsA reduces the phosphorylation of PDHA1 by reducing the activity of PDK1, but not affecting its expression.
HsA decreases PDK1 activity by interfering with the lipoamide-binding domain of the PDH E2 subunit (PDH-E2)
To elucidate the mechanism underlying the inhibitory effect of HsA on PDK1 activity, the interaction and the binding affinity between PDK1 and HsA was analyzed by in silico modeling. The modeled structure of PDK1 with HsA has shown with ribbon and surface representations indicated that HsA bound to Phe78, Gln61 and Thr74 residues of PDK1 (Fig. 3A,B; Lys246 and Asn247 residues of PDK2; Tyr155, Gly325 and Tyr326 residues of PDK3; Arg170, Glu254 and Tyr340 residues of PDK4 (Fig. S3). Among the PDK isoforms, HsA was predicted to bind adjacent to the hydrophobic residues of PDK1 (Leu57, Phe65, and Phe78), which residues participating in the lipoamide-binding pocket18. Next, an isothermal titration calorimeter (ITC) approach was used to confirm the binding ability of HsA and PDK1. The results showed that HsA bound physically to PDK1 with an apparent dissociation constant (KD) of 22 μM (Fig. 3C). To elucidate the precise mode of binding inhibition, the binding affinities between PDK1 protein and lipoamide-binding domains of PDH-E2 (L1 and L2) with or without HsA were measured by ITC. The KD values for the PDK1 interactions with the ligands (L1, L1-HsA, L2, and L2-HsA) were determined to be 41.15 μM, 43.10 μM, 30.03 μM, and 40.98 μM, respectively (Fig. S4). The results indicated that the interaction between PDK1 and the L2 domain of PDH-E2 was reduced in the presence of HsA. To confirm the in vitro interaction data, an intracellular interaction assay between PDK1 and PDH-E2 was conducted using the overexpression of glutathione S-transferase (GST) tagged-PDK1. The results demonstrated that HsA decreased the association of GST tagged-PDK1 with PDH-E2 (Fig. 3D). Consequently, the interaction of PDK1 with PDHA1 proteins was also reduced. These results further establish that HsA inhibits the activity of PDK1 by interfering with the interaction between PDK1 and the L2 lipoamide domain of PDH-E2.
HsA increases the mitochondrial reactive oxygen species (ROS) levels and induces apoptosis of DLD-1 cells
PDK1 inhibition induces mitochondrial-pathway apoptosis via increased phosphorylation byproducts such as ROS19,20. Thus, to determine whether the cytotoxic effects of HsA are associated with the mitochondrial ROS production, DLD-1 cells were treated with Mito-tempo, a mitochondria-targeted antioxidant, and mitochondria ROS was measured by Mito-sox assay. As shown in Fig. 4A, mitochondria ROS levels were increased by HsA treatment. The mitochondrial ROS production and cytotoxicity induced by HsA treatment were rescued by Mito-tempo treatment (Fig. 4B,C). O2 consumption rate was also improved by HsA treatment (Fig. 4D). In the same condition, the increase of the O2 consumption rate and the reduction of phosphorylation of PDHA were higher than that treated with a well-known PDK inhibitor, DCA (Fig. S5). The intracellular ATP level was decreased by treatment with HsA (Fig. 4E). As a consequence of increased mitochondrial ROS, HsA also collapsed the mitochondrial membrane potential (Fig. 5A) and induced apoptotic cell death (Fig. 5B) in DLD-1 cells. The Bax/Bcl-2 ratio, an important marker of mitochondrial membrane depolarization, was also increased by HsA treatment (Fig. 5C). Finally, HsA increased the activation of caspase-9, caspase-3, and PARP, indicating the activation of the mitochondrial pathway for apoptosis. To validate the specificity of HsA for PDK1, pLKO.1, and PDK1 silencing DLD-1 cells were used (Fig. S5D)21. The anti-tumor effect of HsA was suppressed in PDK1 silencing DLD-1 cells (Fig. S5E). All these results indicate that HsA induces apoptosis of colon cancer cells through ROS-mediated mitochondrial damage.
HsA reduces in vivo tumor growth in the allograft model
To further confirm the effect of HsA we have seen in vitro, we injected a murine colorectal cancer cell line, CT26 cells, into immunocompetent BALB/c mice to create an allograft CRC model. From the 8th day of tumor injection, HsA (0, 1, 10 mg/kg/day) was treated for 10 days. The average tumor size when HsA started to treat was about 111.85 mm3. Tumor volume was suppressed by HsA (Fig. 6A), but HsA did not cause significant weight loss (Fig. S6A). Then, the tumor tissue specimens were removed from the sacrificed mice, and images were taken (Fig. 6B). HsA showed a significant effect in suppressing the growth of CT26 cells in a dose-dependent manner as seen by the reduced tumor volume and weight (Fig. 6D–E). Finally, we measured the activity of HsA on PDK1 in animal models, the phosphorylation of PDHA1 was determined by Western blot analysis. Consistent with the in vitro experiments, HsA decreased the phosphorylation of PDHA1 in allograft tumor tissues in a dose-dependent manner. Moreover, activation of caspase-9 and caspase-3 was also induced by treatment with HsA (Fig. 6F). Considering there little or less hepatocellular or renal toxicity, HsA suppressed the growth of CT26 cells by reducing PDK1 activity (Fig. S6B–D). These results suggest that HsA has an inhibitory effect on PDK1 activity and consequently reduces the growth of CT26 cells in the murine allograft model.
Discussion
In this study, we focus on targeting PDK1 and suppressing the growth of glycolytic tumors. We showed that HsA reduced the growth of several CRC cells by suppressing the kinase activity of PDK1 at both in vitro and in vivo levels. HsA interfered with the binding between PDK1 and the L2 lipoamide domain of PDH-E2, consequently dephosphorylated and activated the PDHA1. The activated PDH complex upon HsA treatment rewired the cancer metabolism from lactic fermentation to OXPHOS, thereby increased the ROS production and mitochondrial depolarization, and ultimately resulted in apoptotic cell death (Fig. 6E). These data demonstrated a good correlation with previous studies that PDK1 is regarded as a crucial point in tilting the energy balance in the favor of cancer cells22,23. Furthermore, PDK1 inhibitors were used in co-treatment with other drugs, as previously shown that inhibition of PDK1 improves the anti-cancer effects of EGFR tyrosine kinase inhibitors24.
Inhibition of PDKs increases the mitochondrial production of the electron-donor NADH, a substrate of the ETC complex I, causing complex I dysfunction in cancer cells23. Once the O2 consumption is uncoupled with ATP synthesis, the oxidative stress increases significantly and produces cellular damages25,26. The knockdown of PDK1 could also increase mitochondrial oxygen consumption and inhibit tumor proliferation by activating apoptosis11,27. However, PDK1 is reported to be expressed at low levels in most of the normal tissues and energy consumption in normal cells relies mainly on mitochondrial OXPHOS4,28. Thus, inhibition of PDK1 would not cause serious problems in normal cells.
Crystal structure studies revealed that the three domains of PDKs, including the pyruvate-binding domain (N-terminal regulatory domain), lipoamide-binding domain, and nucleotide-binding domain (C-terminal catalytic domain), are important for the regulation of PDK activity29,30. PDKs are engaged by the PDH complex by precise binding to the inner lipoamide domain of the PDH-E2/E3 binding protein (E3BP) core, and they effectively phosphorylate the PDHA131. PDK1 strongly binds to the L2 lipoamide domain of PDH-E2 and more weakly to the L1 lipoamide domain. The L3 domain of E3BP does not interact with PDK129. In this study, the computational prediction and biochemical assay demonstrated that HsA interfered with the binding of PDK1 to the L2 lipoamide domain of PDH-E2. This mode of action is similar to that of the other established PDK inhibitors, including AZD7545 and Nov3r18,29. However, HsA does not share the characteristics in chemical structure with these established inhibitors of the lipoamide-binding domain.
Several established small molecule inhibitors of PDK1 have been developed. For example, AZD754532, Nov3r33 targets the lipoamide-binding pocket; radicicol34, VER-24660835, and JX0636 targets the ATP-binding pocket; DCA37 binds to pyruvate-binding pocket. However, very limited PDK1 inhibitors are now developing as an anticancer drug. No studies have investigated the anticancer effect of AZD7545, Nov3r, or VER-246608. DCA and JX06 have been reported to reduce cancer growth through modulating metabolism and inducing apoptosis36,38. Recently, compound 10, a novel PDK inhibitor targeting lipoamide-binding pocket has successfully reduced the growth of several cancer cells39. In the present study, we could not precisely determine the in vitro inhibitory efficacy of HsA on the PDK1 activity. However, the IC50 of HsA on cancer growth is comparable to that of previously established PDK inhibitors, such as DCA (over 10 mM), JX06 (4 μM to HT-29 cells), and compound 10 (45.35 μM to HCT-116 cells)36,38,39. Also, typical oral and parenteral daily doses of DCA or JX06 was ranged from 10 to 50 mg/kg or 40 to 80 mg/kg, respectively36,40. In vivo efficacy of compound 10 was not tested. In this study, HsA could suppress significantly the growth of CT26 cells at the concentration of 10 mg/kg.
However, this study has several limitations as follows. First, this study adopted an allograft cancer model using only one CRC cells. To ensure the in vivo anti-cancer efficacy of HsA, a further extensive study using various types of human cancer cells using in vivo xenograft model should be performed. Second, like other natural products41, HsA might bind to the other molecular targets, such as previously reported Nrf2 and NF-κB in inflammation and hepatic fibrosis42,43, and AMPK in liver cancer44. AMPK could be regulated by Acetyl-CoA or ATP production which is regulated by PDK inhibitors45,46. AMPK also might regulate the expression or activity of PDKs47,48. To elucidate the relationship between AMPK and PDK regulation by HsA, further extensive molecular experiments should be conducted. Furthermore, to verify the possibility of developing an anticancer drug, the in vivo safety and pharmacological property of HsA also should be examined in further studies. Despite these limitations, we suggest that HsA might be a potent candidate for developing anti-metabolic cancer drugs because HsA has a comparable in vivo efficacy and a unique structural feature compared to previously established PDK1 inhibitors. Natural products could be a valuable starting point for drug discovery by enhancing the efficacy and target specificity49.
In summary, HsA suppresses the growth of CRC cells in both in vitro and in vivo models by inhibiting the PDK1 activity, thereby enhancing the metabolic shift from glycolysis to OXPHOS, and consequently inducing mitochondrial ROS-mediated apoptosis. We also confirmed that HsA achieves its inhibitory action on PDK1 by targeting its lipoamide-binding pocket. Although more pharmacological studies and clinical evidence are required, HsA has shown a potential candidate as a novel PDK1 inhibitor for colorectal cancer treatment.
Methods
Antibodies and reagents
Antibodies used for western blotting are indicated in Table S1. NAC was purchased from Amresco (Solon, OH, USA). 3-(4,5-Dimethylthiazol-2-yl)2,5-diphenyltetrazolium bromide (MTT), oligomycin, and DCA were supplied by Sigma-Aldrich (St. Louis, MO). All the other chemicals were provided by Sigma-Aldrich unless otherwise indicated. HsA used in this study was a deposit from our previous study16.
Cell culture
Human colon cancer cell lines, SW480 and RKO, were obtained from American Type Culture Collection (Manassas, VA). The other cells were supplied by Korean Cell Line Bank (Seoul, Korea). All the complete growth media were supplemented with 10% heat-inactivated fetal bovine serum (FBS; Sigma-Aldrich) and 1% penicillin/streptomycin (Gibco, Rockville, MD). The cells were incubated in a cell culture incubator at 37 °C in 5% CO2 and 100% humidity conditions.
Cell viability assay
Cell viability was examined using the MTT assay. The cells were seeded on 24-well culture plates (1 × 105 cells/well) and then treated with various concentrations of drugs for 24 h or 48 h. MTT solution (2.0 mg/mL) was added to each well of the plates and the culture plates were incubated for 4 h at 37 °C and 5% CO2 conditions. The culture medium was removed and the number of formazan crystals formed in the living cells was determined by measuring the absorbance at 540 nm with a Spectramax M2 microplate reader (Molecular Devices, San Jose, CA, USA).
Lactate production assay
Lactate production in DLD-1 cells was measured with a lactate fluorometric assay kit (Biovision, CA, USA), as previously described50.
LDHA activity assay
LDHA activity was determined by measuring the NADH oxidation as described in a previous study51. Recombinant LDHA protein (10 ng) was used for the in vitro LDHA assay and 1 μg of total protein from the cell lysates was used for the intracellular LDHA assay. Various concentrations of HsA were added into the reaction solution containing 20 μM NADH, 20 mM HEPES (pH 7.2), 2 mM pyruvate, and 0.05% bovine serum albumin (BSA). In the case of the intracellular assay, HsA was added to the cells. The amount of NADH was measured using the Spectramax M2 spectrofluorometric (Molecular Devices) with 340 nm/360 nm of excitation/emission wavelengths. The activity of LDHA was inversely calculated from the amount of NADH consumption.
PDK1 substrate binding assay
GST and GST-PDK1 construct (obtained from Professor Jing Chen, Emory University) were transfected into HEK 293 T cells using polyethylenimine. After 24 h of transfection, cells were treated with 10 μM of HsA. Then, the cells were harvested and lysed. GST and GST-PDK1 were pulled down using Glutathione Sepharose 4B beads (Amersham Bioscience). The beads were washed with 20 mM potassium phosphate (pH 7). The samples were run on an SDS-PAGE gel, followed by immunoblotting.
Oxygen consumption assay
Oxygen consumption in DLD-1 cells was measured with an oxygen consumption rate assay kit (Cayman Chemical, Ann Arbor, MI). DLD-1 cells were seeded in 96-well tissue culture plates at a density of 4 × 104 cells and the experiment was conducted according to the method provided.
ATP bioluminescence assay
ATP activity in DLD-1 cells was measured with an ATP Bioluminescence Assay Kit (Sigma-Aldrich). DLD-1 cells were seeded in 96-well tissue culture plates at a density of 4 × 104 cells and treated with or without HsA for 12 h. The experiment was conducted according to the method provided.
Measurement of mitochondrial ROS
The production of mitochondrial ROS in cells was determined using MitoSOX Red (Invitrogen, Karlsruhe, Germany). In brief, 1 μM of MitoSOX Red was added to the cells cultured in a conditioned medium and incubated at 37 °C for 10 min. The fluorescence intensity was analyzed using a BD FACS Canto II by measuring the excitation/emission at 510/580 nm wavelengths.
Mitochondrial depolarization assay
Pre-treated DLD-1 cells were incubated with 250 nM TMRM (Thermo Fisher Scientific) for 30 min. The cells were washed with phosphate-buffered saline (PBS). The fluorescent images of the samples were observed and captured using a fluorescence microscope (Zeiss AX10 Imager.M1; Carl Zeiss Microimaging, Oberkochen, Germany) with excitation/emission at 535/600 nm wavelengths. To quantify the mitochondrial membrane potential, the fluorescence intensity of each captured image was calculated using Image J (NIH, MD).
Detection of apoptotic cells
Apoptotic cells were examined using an annexin V-FITC apoptosis detection kit (Life Technologies, Carlsbad, CA). The cells (5 × 105) were resuspended in 500 µL of binding buffer and incubated with 5 µL of annexin V-FITC and propidium iodine (PI) for 15 min at room temperature. The fluorescence intensities of the samples were examined using a BD FACS Canto II flow cytometer by measuring the annexin V-FITC excitation/emission at the wavelengths of 494/518 nm and PI at the wavelengths of 535/617 nm.
Animals and tumor allografts
Male BALB/c mice (6-weeks-old, weight 20–24 g, n = 8 per group) were obtained from Orient Bio Inc. (Sungnam, Korea). All the experimental procedures followed the Guidelines for the Care and Use of Laboratory Animals of the National Institutes of Health of Korea and were approved by the Institutional Animal Care and Use Committee of Pusan National University, Pusan, Republic of Korea (protocol number: PNU-2017-1603). Tumor tissue specimens were immediately removed from the mice and the volumes of tumor tissues were measured with a pair of calipers and were calculated according to the formula [(length × width2)/2]. Murine serum was collected to measure the hepatocellular and renal cytotoxicities using commercial biochemistry analyses from Green Cross Co. (Seoul, Korea).
Statistical analysis
The values from the cell viability, LDH assay, lactate production, and in vivo studies were calculated as percentage values in comparison to the control group and expressed as mean ± standard error of the mean (SEM). The results from the experiments estimating oxygen consumption and ATP rate, mitochondrial membrane potential, and apoptotic cells were calculated as fold change in comparison to the control. Hepatocellular and renal toxicity of the mice were analyzed by one-way analysis of variance with a post hoc Tukey's comparison using GraphPad Prism software (GraphPad Software, San Diego, CA). The minimum level of statistical significance was set at a p-value of 0.05 for all the analyses. All the experiments were independently conducted three times, except for the animal studies. Further details were shown in the supplementary material.
References
Arnold, M. et al. Global patterns and trends in colorectal cancer incidence and mortality. Gut 2016, 2015 (2016).
Vander Heiden, M. G., Cantley, L. C. & Thompson, C. B. Understanding the Warburg effect: the metabolic requirements of cell proliferation. Science 324(5930), 1029–1033 (2009).
Kroemer, G. & Pouyssegur, J. Tumor cell metabolism: cancer’s Achilles’ heel. Cancer Cell 13(6), 472–482 (2008).
Zheng, J. Energy metabolism of cancer: Glycolysis versus oxidative phosphorylation. Oncol. Lett. 4(6), 1151–1157 (2012).
Fang, S. & Fang, X. Advances in glucose metabolism research in colorectal cancer. Biomed. Rep. 5(3), 289–295 (2016).
Holness, M. & Sugden, M. Regulation of Pyruvate Dehydrogenase Complex Activity by Reversible Phosphorylation (Portland Press Limited, Portland, 2003).
Kato, M. et al. Structural basis for inactivation of the human pyruvate dehydrogenase complex by phosphorylation: role of disordered phosphorylation loops. Structure 16(12), 1849–1859 (2008).
Kolobova, E. et al. Regulation of pyruvate dehydrogenase activity through phosphorylation at multiple sites. Biochem. J. 358(1), 69–77 (2001).
Hur, H. et al. Expression of pyruvate dehydrogenase kinase-1 in gastric cancer as a potential therapeutic target. Int. J. Oncol. 42(1), 44–54 (2013).
Qin, L. et al. Targeting PDK1 with dichloroacetophenone to inhibit acute myeloid leukemia (AML) cell growth. Oncotarget 7(2), 1395 (2016).
Liu, T. & Yin, H. PDK1 promotes tumor cell proliferation and migration by enhancing the Warburg effect in non-small cell lung cancer. Oncol. Rep. 37(1), 193–200 (2017).
Schell, J. C. et al. A role for the mitochondrial pyruvate carrier as a repressor of the Warburg effect and colon cancer cell growth. Mol. Cell 56(3), 400–413 (2014).
Kwak, C.-H. et al. Huzhangoside A suppresses tumor growth through inhibition of pyruvate dehydrogenase kinase activity. Cancers 11(5), 712 (2019).
Kwak, C.-H. et al. Ilimaquinone induces the apoptotic cell death of cancer cells by reducing pyruvate dehydrogenase kinase 1 activity. Int. J. Mol. Sci. 21(17), 6021 (2020).
Jang, D. S. et al. Hemistepsins with cytotoxic activity from Hemisteptia lyrata. Planta Med. 65(08), 765–766 (1999).
Kim, J. K. et al. Hemistepsin A ameliorates acute inflammation in macrophages via inhibition of nuclear factor-κB and activation of nuclear factor erythroid 2-related factor 2. Food Chem. Toxicol. 111, 176–188 (2018).
Feron, O. Pyruvate into lactate and back: from the Warburg effect to symbiotic energy fuel exchange in cancer cells. Radiother. Oncol. 92(3), 329–333 (2009).
Kato, M. et al. Distinct structural mechanisms for inhibition of pyruvate dehydrogenase kinase isoforms by AZD7545, dichloroacetate, and radicicol. Structure 15(8), 992–1004 (2007).
Michelakis, E. D., Webster, L. & Mackey, J. R. Dichloroacetate (DCA) as a potential metabolic-targeting therapy for cancer. Br. J. Cancer 99(7), 989–994 (2008).
Yadav, N. et al. Oxidative phosphorylation-dependent regulation of cancer cell apoptosis in response to anticancer agents. Cell Death Dis. 6, e1969 (2015).
Hitosugi, T. et al. Tyrosine phosphorylation of mitochondrial pyruvate dehydrogenase kinase 1 is important for cancer metabolism. Mol. Cell 44(6), 864–877 (2011).
Kim, J.-W. & Dang, C. V. Cancer’s molecular sweet tooth and the Warburg effect. Can. Res. 66(18), 8927–8930 (2006).
Bonnet, S. et al. A mitochondria-K+ channel axis is suppressed in cancer and its normalization promotes apoptosis and inhibits cancer growth. Cancer Cell 11(1), 37–51 (2007).
Yang, Z. et al. Inhibition of pyruvate dehydrogenase kinase 1 enhances the anti-cancer effect of EGFR tyrosine kinase inhibitors in non-small cell lung cancer. Eur. J. Pharmacol. 838, 41–52 (2018).
Kushnareva, Y., Murphy, A. N. & Andreyev, A. Complex I-mediated reactive oxygen species generation: modulation by cytochrome c and NAD (P)+ oxidation–reduction state. Biochem. J. 368(2), 545–553 (2002).
Dai, D.-F. et al. Mitochondrial oxidative stress in aging and healthspan. Long. Healthspan 3(1), 6 (2014).
Papandreou, I. et al. HIF-1 mediates adaptation to hypoxia by actively downregulating mitochondrial oxygen consumption. Cell Metab. 3(3), 187–197 (2006).
Jourdan, M. et al. An in vitro model of differentiation of memory B cells into plasmablasts and plasma cells including detailed phenotypic and molecular characterization. Blood 114(25), 5173–5181 (2009).
Jeoung, N. H. Pyruvate dehydrogenase kinases: therapeutic targets for diabetes and cancers. Diabetes Metab. J. 39(3), 188–197 (2015).
Roche, T. E. & Hiromasa, Y. Pyruvate dehydrogenase kinase regulatory mechanisms and inhibition in treating diabetes, heart ischemia, and cancer. Cell Mol. Life Sci. 64(7–8), 830–849 (2007).
Liu, S., Baker, J. C. & Roche, T. E. Binding of the pyruvate dehydrogenase kinase to recombinant constructs containing the inner lipoyl domain of the dihydrolipoyl acetyltransferase component. J. Biol. Chem. 270(2), 793–800 (1995).
Mayers, R. et al. AZD7545, a Novel Inhibitor of Pyruvate Dehydrogenase Kinase 2 (PDHK2), Activates Pyruvate Dehydrogenase in Vivo and Improves Blood Glucose Control in Obese (fa/fa) Zucker Rats (Portland Press Limited, Portland, 2003).
Aicher, T. D. et al. Secondary amides of (R)-3,3,3-trifluoro-2-hydroxy-2-methylpropionic acid as inhibitors of pyruvate dehydrogenase kinase. J. Med. Chem. 43(2), 236–249 (2000).
Soga, S. et al. Development of radicicol analogues. Curr. Cancer Drug Targets 3(5), 359–369 (2003).
Moore, J. D. et al. VER-246608, a novel pan-isoform ATP competitive inhibitor of pyruvate dehydrogenase kinase, disrupts Warburg metabolism and induces context-dependent cytostasis in cancer cells. Oncotarget 5(24), 12862 (2014).
Sun, W. et al. JX06 selectively inhibits pyruvate dehydrogenase kinase PDK1 by a covalent cysteine modification. Cancer Res. 75(22), 4923–4936 (2015).
Li, J., Kato, M. & Chuang, D. T. Pivotal role of the C-terminal DW-motif in mediating inhibition of pyruvate dehydrogenase kinase 2 by dichloroacetate. J. Biol. Chem. 284(49), 34458–34467 (2009).
Stockwin, L. H. et al. Sodium dichloroacetate selectively targets cells with defects in the mitochondrial ETC. Int J Cancer 127(11), 2510–2519 (2010).
Zhang, W. et al. Identification of novel pyruvate dehydrogenase kinase 1 (PDK1) inhibitors by kinase activity-based high-throughput screening for anticancer therapeutics. ACS Combin. Sci. 20(11), 660–671 (2018).
Stacpoole, P. W. Therapeutic targeting of the pyruvate dehydrogenase complex/pyruvate dehydrogenase kinase (PDC/PDK) axis in cancer. J. Natl. Cancer Inst. 109, 11 (2017).
Venkatraman, P. Specificity in the interaction of natural products with their target proteins- a biochemical and structural insight. Mini Rev. Med. Chem. 10(6), 540–549 (2010).
Kim, J. K. et al. Hemistepsin A alleviates liver fibrosis by inducing apoptosis of activated hepatic stellate cells via inhibition of nuclear factor-kappaB and Akt. Food Chem. Toxicol. 135, 111044 (2020).
Kim, J. K. et al. Hemistepsin A ameliorates acute inflammation in macrophages via inhibition of nuclear factor-kappaB and activation of nuclear factor erythroid 2-related factor 2. Food Chem. Toxicol. 111, 176–188 (2018).
Baek, S. Y. et al. Hemistepsin A inhibits cell proliferation and induces G0/G1-phase arrest, cellular senescence and apoptosis via the AMPK and p53/p21 signals in human hepatocellular carcinoma. Biomolecules 10, 5 (2020).
Saunier, E. et al. Resveratrol reverses the Warburg effect by targeting the pyruvate dehydrogenase complex in colon cancer cells. Sci. Rep. 7, 1 (2017).
Marino, G. et al. Regulation of autophagy by cytosolic acetyl-coenzyme A. Mol. Cell 53(5), 710–725 (2014).
Klein, D. K. et al. Lack of AMPK alpha 2 enhances pyruvate dehydrogenase activity during exercise. Am. J. Physiol. Endocrinol. Metab. 293(5), E1242–E1249 (2007).
Jeong, J. Y. et al. Transcriptional regulation of pyruvate dehydrogenase kinase. Diabetes Metab. J. 36(5), 328–335 (2012).
Rodrigues, T. et al. Counting on natural products for drug design. Nat. Chem. 8(6), 531–541 (2016).
Fan, J. et al. Tyrosine phosphorylation of lactate dehydrogenase a is important for NADH/NAD+ redox homeostasis in cancer cells. Mol. Cell. Biol. 31(24), 4938–4950 (2011).
Chung, T.-W. et al. Anemone rivularis inhibits pyruvate dehydrogenase kinase activity and tumor growth. J. Ethnopharmacol. 203, 47–54 (2017).
Acknowledgements
This work was supported by a grant from the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (MISP), of the Korean Government (Grant No. 2014R1A5A20009936 and 2019R1A2C2003624).
Author information
Authors and Affiliations
Contributions
K.T.H. conceived and supervised the project. L.J. performed major experiments and collected the data. E.Y.K, T.W.C, and S.J.B. analyzed the data and conducted the animal study. J.H.H assisted the biochemical analysis and animal study. J.R.L. and Y.W.K. isolated and supplied HsA. C.W.H., S.Y.P. and S.B.J. perform and analyzed the computational simulation and ITC analysis. L.J. and K.T.H. wrote the manuscript. All the authors reviewed the manuscript and agreed to the submission.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Jin, L., Kim, EY., Chung, TW. et al. Hemistepsin A suppresses colorectal cancer growth through inhibiting pyruvate dehydrogenase kinase activity. Sci Rep 10, 21940 (2020). https://doi.org/10.1038/s41598-020-79019-1
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-020-79019-1
This article is cited by
-
Targeting pyruvate dehydrogenase kinase 1 overcomes EGFR C797S mutation-driven osimertinib resistance in non-small cell lung cancer
Experimental & Molecular Medicine (2024)
-
p53 Orchestrates Cancer Metabolism: Unveiling Strategies to Reverse the Warburg Effect
Bulletin of Mathematical Biology (2024)
-
A novel organic arsenic derivative MZ2 remodels metabolism and triggers mtROS-mediated apoptosis in acute myeloid leukemia
Journal of Cancer Research and Clinical Oncology (2023)