The pivotal role of pyruvate dehydrogenase kinases in metabolic flexibility
Open accessAbstract
Metabolic flexibility is the capacity of a system to adjust fuel (primarily glucose and fatty acids) oxidation based on nutrient availability. The ability to alter substrate oxidation in response to nutritional state depends on the genetically influenced balance between oxidation and storage capacities. Competition between fatty acids and glucose for oxidation occurs at the level of the pyruvate dehydrogenase complex (PDC). The PDC is normally active in most tissues in the fed state, and suppressing PDC activity by pyruvate dehydrogenase (PDH) kinase (PDK) is crucial to maintain energy homeostasis under some extreme nutritional conditions in mammals. Conversely, inappropriate suppression of PDC activity might promote the development of metabolic diseases. This review summarizes PDKs' pivotal role in control of metabolic flexibility under various nutrient conditions and in different tissues, with emphasis on the best characterized PDK4. Understanding the regulation of PDC and PDKs and their roles in energy homeostasis could be beneficial to alleviate metabolic inflexibility and to provide possible therapies for metabolic diseases, including type 2 diabetes (T2D).
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Competition between fatty acids and glucose occurs at the level of the pyruvate dehydrogenase complex.
“competition between fatty acids and glucose occurs at the level of the pyruvate dehydrogenase complex”
From Metabolic Flexibility as an Adaptation to Energy Resources and Requirements in Health and Disease (2018) · cites this paper as [314]
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Cancer cell metabolism: warburg and beyond
Hsu, P. P., & Sabatini, D. M. (2008) · Cell · doi:10.1016/j.cell.2008.08.021 · Cited by 2,452 · see citing works
Fuel selection in human skeletal muscle in insulin resistance: a reexamination.
Kelley, D. E., & Mandarino, L. J. (2000) · Diabetes · doi:10.2337/diabetes.49.5.677 · Cited by 1,017 · see citing works
Yao, J., Irwin, R. W., Zhao, L., Nilsen, J., Hamilton, R. T., & Brinton, R. D. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903563106 · Cited by 940 · see citing works
Metabolic Modulation of Glioblastoma with Dichloroacetate
Michelakis, E. D., Sutendra, G., Dromparis, P., Webster, L., Haromy, A., Niven, E. B., Maguire, C., Gammer, T.-L., Mackey, J. R., Fulton, D. S., et al. (2010) · Science Translational Medicine · doi:10.1126/scitranslmed.3000677 · Cited by 722 · see citing works
Non-CpG methylation of the PGC-1α promoter through DNMT3B controls mitochondrial density.
Barrès, R., Osler, M. E., Yan, J., Rune, A., Fritz, T., Caidahl, K., Krook, A., & Zierath, J. R. (2009) · Cell Metabolism · doi:10.1016/j.cmet.2009.07.011 · Cited by 602 · see citing works
The role of FoxO in the regulation of metabolism
Gross, D. N., van den Heuvel, A. P. J., & Birnbaum, M. J. (2008) · Oncogene · doi:10.1038/onc.2008.25 · Cited by 555 · see citing works
Metabolic flexibility and insulin resistance
Galgani, J. E., Moro, C., & Ravussin, E. (2008) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.90558.2008 · Cited by 532 · cited 2× · see citing works
“The capacity for an organism to adapt fuel oxidation to fuel availability, that is, to preferentially utilize carbohydrate and lipid fuels and to be able to rapidly switch between them is termed metabolic flexibility [2,3].”
Regulation of pyruvate dehydrogenase complex activity by reversible phosphorylation
Holness, M. J., & Sugden, M. C. (2003) · Biochemical Society Transactions · doi:10.1042/bst0311143 · Cited by 479 · see citing works
Malonyl-CoA: the regulator of fatty acid synthesis and oxidation
Foster, D. W. (2012) · Journal of Clinical Investigation · doi:10.1172/jci63967 · Cited by 358 · see citing works
Wende, A. R., Huss, J. M., Schaeffer, P. J., Giguère, V., & Kelly, D. P. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.24.10684-10694.2005 · Cited by 354 · see citing works
Furuyama, T., Kitayama, K., Yamashita, H., & Mori, N. (2003) · Biochemical Journal · doi:10.1042/bj20030022 · Cited by 326 · see citing works
Randle, P. J. (1986) · Biochemical Society Transactions · doi:10.1042/bst0140799 · Cited by 313 · see citing works
Storlien, L., Oakes, N. D., & Kelley, D. E. (2004) · Proceedings of the Nutrition Society · doi:10.1079/pns2004349 · Cited by 291 · see citing works
Wu, P., Inskeep, K., Bowker-Kinley, M. M., Popov, K. M., & Harris, R. A. (1999) · Diabetes · doi:10.2337/diabetes.48.8.1593 · Cited by 290 · see citing works
Diversity of the Pyruvate Dehydrogenase Kinase Gene Family in Humans
Gudi, R., Bowker-Kinley, M. M., Kedishvili, N. Y., Zhao, Y., & Popov, K. M. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.48.28989 · Cited by 287 · see citing works
Sugden, M. C., & Holness, M. J. (2006) · Archives of Physiology and Biochemistry · doi:10.1080/13813450600935263 · Cited by 281 · see citing works
Roche, T. E., & Hiromasa, Y. (2007) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-007-6380-z · Cited by 265 · see citing works
Pyruvate dehydrogenase kinase as a novel therapeutic target in oncology
Sutendra, G., & Michelakis, E. D. (2013) · Frontiers in Oncology · doi:10.3389/fonc.2013.00038 · Cited by 263 · see citing works
Brøns, C., Jacobsen, S. B., Nilsson, E., Rönn, T., Jensen, C. B., Storgaard, H., Poulsen, P., Groop, L., Ling, C., Astrup, A. V., et al. (2010) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2009-2413 · Cited by 193 · see citing works
Glyceroneogenesis Is the Dominant Pathway for Triglyceride Glycerol Synthesis in Vivo in the Rat
Nye, C. K., Hanson, R. W., & Kalhan, S. C. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m804393200 · Cited by 182 · see citing works
Transcriptional Regulation of Pyruvate Dehydrogenase Kinase
Jeong, J. Y., Jeoung, N. H., Park, K., & Lee, I. K. (2012) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2012.36.5.328 · Cited by 179 · see citing works
Holness, M. J., Kraus, A., Harris, R. A., & Sugden, M. C. (2000) · Diabetes · doi:10.2337/diabetes.49.5.775 · Cited by 169 · see citing works
Mori, J., Alrob, O. A., Wagg, C. S., Harris, R. A., Lopaschuk, G. D., & Oudit, G. Y. (2013) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00636.2012 · Cited by 168 · see citing works
Jeoung, N. H., & Harris, R. A. (2008) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00536.2007 · Cited by 162 · see citing works
Connaughton, S., Chowdhury, F., Attia, R. R., Song, S., Zhang, Y., Elam, M. B., Cook, G. A., & Park, E. A. (2009) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2009.08.011 · Cited by 144 · see citing works
Role of pyruvate dehydrogenase kinase isoenzyme 4 (PDHK4) in glucose homoeostasis during starvation
Jeoung, N. H., Wu, P., Joshi, M., Jaskiewicz, J. A., Bock, C. B., DePaoli-Roach, A. A., & Harris, R. A. (2006) · Biochemical Journal · doi:10.1042/bj20060125 · Cited by 143 · see citing works
Clinical pharmacology and toxicology of dichloroacetate.
Stacpoole, P. W., Henderson, G. N., Yan, Z., & James, M. O. (1998) · Environmental Health Perspectives · doi:10.1289/ehp.98106s4989 · Cited by 141 · see citing works
Fuel economy in food‐deprived skeletal muscle: signaling pathways and regulatory mechanisms
de Lange, P., Moreno, M., Silvestri, E., Lombardi, A., Goglia, F., & Lanni, A. (2007) · The FASEB Journal · doi:10.1096/fj.07-8527rev · Cited by 133 · see citing works
Pilegaard, H., & Neufer, P. D. (2004) · Proceedings of The Nutrition Society · doi:10.1079/pns2004345 · Cited by 133 · see citing works
Nahlé, Z., Hsieh, M., Pietka, T., Coburn, C. T., Grimaldi, P. A., Zhang, M. Q., Das, D., & Abumrad, N. A. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m706478200 · Cited by 122 · see citing works
Huang, B., Wu, P., Popov, K. M., & Harris, R. A. (2003) · Diabetes · doi:10.2337/diabetes.52.6.1371 · Cited by 122 · see citing works
Sugden, M. C., & Holness, M. J. (1994) · The FASEB Journal · doi:10.1096/fasebj.8.1.8299890 · Cited by 122 · see citing works
Zhao, G., Jeoung, N. H., Burgess, S. C., Rosaaen-Stowe, K. A., Inagaki, T., Latif, S., Shelton, J. M., McAnally, J., Bassel‐Duby, R., Harris, R. A., et al. (2007) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00870.2007 · Cited by 120 · see citing works
Kim, Y. I., Lee, F. N., Choi, W. S., Lee, S., & Youn, J. H. (2006) · Diabetes · doi:10.2337/db05-1606 · Cited by 119 · see citing works
Catoire, M., Mensink, M., Boekschoten, M. V., Hangelbroek, R., Müller, M., Schrauwen, P., & Kersten, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051066 · Cited by 116 · see citing works
Pyruvate Dehydrogenase Kinase 4
Cadoudal, T., Distel, E., Durant, S., Fouque, F., Blouin, J., Collinet, M., Bortoli, S., Forest, C. D., & Benelli, C. (2008) · Diabetes · doi:10.2337/db08-0477 · Cited by 110 · see citing works
Wu, C.-A., Chao, Y., Shiah, S., & Lin, W. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.01.025 · Cited by 109 · see citing works
Sugden, M. C., KRAUS, A., Harris, R. A., & Holness, M. J. (2000) · Biochemical Journal · doi:10.1042/bj3460651 · Cited by 107 · see citing works
Skeletal Muscle Lipid Accumulation in Type 2 Diabetes May Involve the Liver X Receptor Pathway
Kase, E. T., Wensaas, A. J., Aas, V., Højlund, K., Levin, K., Thoresen, G. H., Beck‐Nielsen, H., Rustan, A. C., & Gaster, M. (2005) · Diabetes · doi:10.2337/diabetes.54.4.1108 · Cited by 102 · see citing works
Kulkarni, S. S., Salehzadeh, F., Fritz, T., Zierath, J. R., Krook, A., & Osler, M. E. (2011) · Metabolism · doi:10.1016/j.metabol.2011.06.014 · Cited by 94 · see citing works
AZD7545 is a selective inhibitor of pyruvate dehydrogenase kinase 2
Morrell, J., Orme, J. P., Butlin, R. J., Roche, T. E., Mayers, R. M., & Kilgour, E. (2003) · Biochemical Society Transactions · doi:10.1042/bst0311168 · Cited by 86 · see citing works
Sugden, M. C., LANGDOWN, M. L., Harris, R. A., & Holness, M. J. (2000) · Biochemical Journal · doi:10.1042/bj3520731 · Cited by 86 · see citing works
Holness, M. J., Bulmer, K., Smith, N. D., & Sugden, M. C. (2003) · Biochemical Journal · doi:10.1042/bj20021509 · Cited by 85 · see citing works
Role of Pyruvate Dehydrogenase Kinase 4 in Regulation of Blood Glucose Levels
Jeoung, N. H., & Harris, R. A. (2010) · Korean Diabetes Journal · doi:10.4093/kdj.2010.34.5.274 · Cited by 78 · see citing works
Selective modulation of promoter recruitment and transcriptional activity of PPARγ
Sears, D. D., Hsiao, A., Ofrecio, J. M., Chapman, J., He, W., & Olefsky, J. M. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.10.057 · Cited by 70 · see citing works
Regulation of Pyruvate Dehydrogenase Kinase 4 (PDK4) by Thyroid Hormone
Attia, R. R., Connaughton, S., Boone, L. R., Wang, F., Elam, M. B., Ness, G. C., Cook, G. A., & Park, E. A. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.039081 · Cited by 69 · see citing works
Jha, M. K., Jeon, S., & Suk, K. (2012) · Current Neuropharmacology · doi:10.2174/157015912804143586 · Cited by 69 · see citing works
Constantin‐Teodosiu, D., Constantin, D., Stephens, F. B., Laithwaite, D., & Greenhaff, P. L. (2012) · Diabetes · doi:10.2337/db11-0799 · Cited by 65 · see citing works
PPARs and the orchestration of metabolic fuel selection
Sugden, M. C., Zariwala, M. G., & Holness, M. J. (2009) · Pharmacological Research · doi:10.1016/j.phrs.2009.03.014 · Cited by 64 · see citing works
Jha, M. K., Jeon, S., & Suk, K. (2012) · Current Neuropharmacology · doi:10.2174/157015912804499528 · Cited by 64 · see citing works
Araki, M., & Motojima, K. (2006) · FEBS Journal · doi:10.1111/j.1742-4658.2006.05183.x · Cited by 63 · see citing works
Hwang, B., Jeoung, N. H., & Harris, R. A. (2009) · Biochemical Journal · doi:10.1042/bj20090390 · Cited by 63 · see citing works
Tao, R., Xiong, X., Harris, R. A., White, M. F., & Dong, X. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071997 · Cited by 60 · see citing works
Houten, S. M., Chegary, M., Brinke, H. T., Wijnen, W. J., Glatz, J. F. C., Luiken, J. J. F. P., Wijburg, F. A., & Wanders, R. J. A. (2009) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-9066-x · Cited by 52 · see citing works
Nellemann, B., Vendelbo, M. H., Nielsen, T. S., Bak, A. M., Høgild, M. L., Pedersen, S. B., Biensø, R. S., Pilegaard, H., Møller, N., Jessen, N., et al. (2013) · Acta Physiologica · doi:10.1111/apha.12183 · Cited by 51 · see citing works
Poplawski, M. M., Mastaitis, J. W., Yang, X.-J., & Mobbs, C. V. (2010) · Endocrinology · doi:10.1210/en.2010-0702 · Cited by 50 · see citing works
Rinnankoski‐Tuikka, R., Silvennoinen, M., Karvinen, S. M., Hulmi, J. J., Lehti, M., Kivelä, R., Reunanen, H., & Kainulainen, H. (2012) · Nutrition & Metabolism · doi:10.1186/1743-7075-9-53 · Cited by 49 · see citing works
Short-term regulation of the mammalian pyruvate dehydrogenase complex.
Strumiło, S. (2005) · Acta Biochimica Polonica · doi:10.18388/abp.2005_3387 · Cited by 48 · see citing works
Epinephrine-mediated regulation of PDK4 mRNA in rat adipose tissue
Wan, Z., Thrush, A. B., Legare, M., Frier, B. C., Sutherland, L., Williams, D. B., & Wright, D. C. (2010) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00188.2010 · Cited by 48 · see citing works
Regulation of PDK mRNA by high fatty acid and glucose in pancreatic islets
Xu, J., Han, J., Epstein, P. N., & Liu, Y. Q. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.03.211 · Cited by 44 · see citing works
Caton, P., Holness, M. J., Bishop‐Bailey, D., & Sugden, M. C. (2011) · Biochemical Journal · doi:10.1042/bj20110702 · Cited by 42 · see citing works
Eivers, S. S., McGivney, B. A., Gu, J., MacHugh, D. E., Katz, L. M., & Hill, E. W. (2011) · Animal Genetics · doi:10.1111/j.1365-2052.2011.02238.x · Cited by 41 · see citing works
Sugden, M. C. (2003) · Obesity Research · doi:10.1038/oby.2003.26 · Cited by 36 · see citing works
Metabolomic analysis of pancreatic beta cells following exposure to high glucose
Wallace, M., Whelan, H., & Brennan, L. (2012) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2012.10.025 · Cited by 33 · see citing works
Arumugam, R., Horowitz, E., Noland, R. C., Lu, D., Fleenor, D. E., & Freemark, M. (2010) · Endocrinology · doi:10.1210/en.2010-0049 · Cited by 32 · see citing works
Regulation of Pyruvate Dehydrogenase Kinase 4 (PDK4) by CCAAT/Enhancer-binding Protein β (C/EBPβ)
Attia, R. R., Sharma, P., Janssen, R. C., Friedman, J. E., Deng, X., Lee, J., Elam, M. B., Cook, G. A., & Park, E. A. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.246389 · Cited by 31 · see citing works
Ding, F., Li, H. H., Li, J. Z., Myers, R., & Francke, U. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009402 · Cited by 30 · see citing works
Kim, Y. D., Kim, Y., Tadi, S., Yu, J. H., Yim, Y., Jeoung, N. H., Shong, M., Hennighausen, L. G., Harris, R. A., Lee, I., et al. (2012) · Diabetes · doi:10.2337/db11-1665 · Cited by 28 · see citing works
Akhmedov, D., Marchi, U. D., Wollheim, C. B., & Wiederkehr, A. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2012.07.005 · Cited by 25 · see citing works
Nakai, N., Obayashi, M., Nagasaki, M., Sato, Y., Fujitsuka, N., Yoshimura, A., Miyazaki, Y., Sugiyama, S., & Shimomura, Y. (2000) · Life Sciences · doi:10.1016/s0024-3205(00)00947-4 · Cited by 24 · see citing works
Zhang, L., Mori, J., Wagg, C. S., & Lopaschuk, G. D. (2012) · FEBS Letters · doi:10.1016/j.febslet.2012.02.027 · Cited by 23 · see citing works
Sugden, M. C., Lall, H., Harris, R., & Holness, M. J. (2000) · Journal of Endocrinology · doi:10.1677/joe.0.1670339 · Cited by 23 · see citing works
Epinephrine Induces PDK4 mRNA Expression in Adipose Tissue From Obese, Insulin Resistant Rats
Wan, Z., Frier, B. C., Williams, D. B., & Wright, D. C. (2011) · Obesity · doi:10.1038/oby.2011.252 · Cited by 19 · see citing works
Role of pyruvate dehydrogenase kinase 4 in regulating PDH activation during acute muscle contraction
Herbst, E. A. F., Dunford, E. C. E., Harris, R. A., Vandenboom, R., LeBlanc, P. J., Roy, B. D., Jeoung, N. H., & Peters, S. J. (2012) · Applied Physiology Nutrition and Metabolism · doi:10.1139/h11-136 · Cited by 19 · see citing works
Hwang, B., Wu, P., & Harris, R. A. (2012) · FEBS Journal · doi:10.1111/j.1742-4658.2012.08569.x · Cited by 14 · see citing works
Sugden, M. C., Fryer, L. G. D., Priestman, D. A., Orfali, K. A., & Holness, M. J. (1996) · Molecular and Cellular Endocrinology · doi:10.1016/0303-7207(96)03817-8 · Cited by 13 · see citing works
Holness, M. J., Zariwala, M. G., Walker, C. G., & Sugden, M. C. (2012) · FEBS Open Bio · doi:10.1016/j.fob.2012.02.003 · Cited by 12 · see citing works
Randle (1998) · doi:10.1002/(sici)1099-0895(199812)14:4
Flagged first, then by citations
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Sorted by citations
Metabolic Flexibility as an Adaptation to Energy Resources and Requirements in Health and Disease
Smith, R. L., Soeters, M. R., Wüst, R. C. I., & Houtkooper, R. H. (2018) · Endocrine Reviews · doi:10.1210/er.2017-00211 · Cited by 787 · see citing works
Judge, A., & Dodd, M. S. (2020) · Essays in Biochemistry · doi:10.1042/ebc20190041 · Cited by 373 · see citing works
Efferocytosis induces a novel SLC program to promote glucose uptake and lactate release
Morioka, S., Perry, J. S. A., Raymond, M. H., Medina, C. B., Zhu, Y., Zhao, L., Serbulea, V., Önengüt-Gümüşcü, S., Leitinger, N., Kucenas, S., et al. (2018) · Nature · doi:10.1038/s41586-018-0735-5 · Cited by 370 · see citing works
Atlas of Circadian Metabolism Reveals System-wide Coordination and Communication between Clocks
Dyar, K. A., Lutter, D., Artati, A., Ceglia, N., Liu, Y., Armenta, D., Jastroch, M., Schneider, S., de Mateo, S., Cervantes, M., et al. (2018) · Cell · doi:10.1016/j.cell.2018.08.042 · Cited by 335 · see citing works
PDK4 augments ER-mitochondria contact to dampen skeletal muscle insulin signaling during obesity
Thoudam, T., Ha, C.-M., Leem, J., Chanda, D., Park, J.-S., Kim, H.-J., Jeon, J.-H., Choi, Y.-K., Liangpunsakul, S., Huh, Y. H., et al. (2019) · Diabetes · doi:10.2337/db18-0363 · Cited by 207 · see citing works
Fluge, Ø., Mella, O., Bruland, O., Risa, K., Dyrstad, S. E., Alme, K., Rekeland, I. G., Sapkota, D., Røsland, G. V., Fosså, A., et al. (2016) · JCI Insight · doi:10.1172/jci.insight.89376 · Cited by 209 · see citing works
Hsu, Y., Wu, Y., Yu, T.-H., & Wei, Y. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.02.011 · Cited by 190 · see citing works
Unique Metabolic Adaptations Dictate Distal Organ-Specific Metastatic Colonization
Schild, T., Low, V., Blenis, J., & Gomes, A. P. (2018) · Cancer Cell · doi:10.1016/j.ccell.2018.02.001 · Cited by 185 · see citing works
FOXK1 and FOXK2 regulate aerobic glycolysis
Sukonina, V., Ma, H., Zhang, W., Bartesaghi, S., Subhash, S., Heglind, M., Foyn, H., Betz, M. J., Nilsson, D., Lidell, M. E., et al. (2019) · Nature · doi:10.1038/s41586-019-0900-5 · Cited by 181 · see citing works
Inak, G., Rybak‐Wolf, A., Lisowski, P., Pentimalli, T. M., Jüttner, R., Glažar, P., Uppal, K., Bottani, E., Brunetti, D., Secker, C., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-22117-z · Cited by 145 · see citing works
α-Hydroxybutyric Acid Is a Selective Metabolite Biomarker of Impaired Glucose Tolerance
Cobb, J. E., Eckhart, A. D., Motsinger‐Reif, A. A., Carr, B., Groop, L., & Ferrannini, E. (2016) · Diabetes Care · doi:10.2337/dc15-2752 · Cited by 129 · see citing works
Imidacloprid Promotes High Fat Diet-Induced Adiposity and Insulin Resistance in Male C57BL/6J Mice
Sun, Q., Xiao, X., Kim, Y., Kim, D., Yoon, K. S., Clark, J. M., & Park, Y. (2016) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.6b04322 · Cited by 132 · see citing works
Nagarajan, S. R., Paul-Heng, M., Krycer, J. R., Fazakerley, D. J., Sharland, A. F., & Hoy, A. J. (2019) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00365.2018 · Cited by 132 · see citing works
Molecular interactions underpinning the phenotype of hibernation in mammals
Andrews, M. T. (2019) · Journal of Experimental Biology · doi:10.1242/jeb.160606 · Cited by 125 · see citing works
The role of DNA methylation in the pathogenesis of type 2 diabetes mellitus
Ahmed, S. A. H., Ansari, S. A., Mensah‐Brown, E. P. K., & Emerald, B. S. (2020) · Clinical Epigenetics · doi:10.1186/s13148-020-00896-4 · Cited by 126 · see citing works
Stimulation of glycolysis promotes cardiomyocyte proliferation after injury in adult zebrafish
Fukuda, R., Marín‐Juez, R., El‐Sammak, H., Beisaw, A., Ramadass, R., Kuenne, C. T., Günther, S., Konzer, A., Bhagwat, A. M., Graumann, J., et al. (2020) · EMBO Reports · doi:10.15252/embr.201949752 · Cited by 119 · see citing works
Oncogenic role of PDK4 in human colon cancer cells
Leclerc, D., Pham, D. N. T., Lévesque, N., Truongcao, M. M., Foulkes, W. D., Sapienza, C., & Rozen, R. R. (2017) · British Journal of Cancer · doi:10.1038/bjc.2017.38 · Cited by 115 · see citing works
The Role of Pyruvate Dehydrogenase Kinase in Diabetes and Obesity
Lee, I. (2014) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2014.38.3.181 · Cited by 111 · see citing works
Fan, Y., Qin, Y., Chen, M., Li, X., Wang, R., Huang, Z., Xu, Q., Yu, M., Zhang, Y., Han, X., et al. (2019) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2019.121534 · Cited by 108 · see citing works
Immunometabolic Endothelial Phenotypes: Integrating Inflammation and Glucose Metabolism
Xiao, W., Oldham, W. M., Priolo, C., Pandey, A. K., & Loscalzo, J. (2021) · Circulation Research · doi:10.1161/circresaha.120.318805 · Cited by 106 · see citing works
Increased oxidative phosphorylation in response to acute and chronic DNA damage
Brace, L. E., Vose, S. C., Stanya, K. J., Gathungu, R. M., Marur, V. R., Longchamp, A., Treviño-Villarreal, H., Mejia, P., Vargas, D., Inouye, K., et al. (2016) · npj Aging and Mechanisms of Disease · doi:10.1038/npjamd.2016.22 · Cited by 105 · see citing works
Pérez, K., Ciotlos, S., McGirr, J., Limbad, C., Doi, R., Nederveen, J. P., Nilsson, M. I., Winer, D. A., Evans, W. J., Tarnopolsky, M. A., et al. (2022) · Aging · doi:10.18632/aging.204435 · Cited by 105 · see citing works
The Implications of PDK1–4 on Tumor Energy Metabolism, Aggressiveness and Therapy Resistance
Atas, E., Oberhuber, M., & Kenner, L. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.583217 · Cited by 104 · see citing works
Pyruvate dehydrogenase kinase 4 deficiency attenuates cisplatin-induced acute kidney injury
Oh, C. J., Ha, C., Choi, Y.-K., Park, S., Choe, M. S., Jeoung, N. H., Huh, Y. H., Kim, H.-J., Kweon, H., Lee, J.-M., et al. (2016) · Kidney International · doi:10.1016/j.kint.2016.10.011 · Cited by 104 · see citing works
Metabolic host response and therapeutic approaches to influenza infection
Keshavarz, M., Solaymani‐Mohammadi, F., Namdari, H., Arjeini, Y., Mousavi, M. J., & Rezaei, F. (2020) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-020-00211-2 · Cited by 99 · see citing works
Lipid metabolism in adaptation to extreme nutritional challenges
Olsen, L. A., Thum, E., & Rohner, N. (2021) · Developmental Cell · doi:10.1016/j.devcel.2021.02.024 · Cited by 99 · see citing works
Deol, P., Evans, J. R., Dhahbi, J. M., Chellappa, K., Han, D. S. C., Spindler, S. R., & Sladek, F. M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0132672 · Cited by 98 · see citing works
Lecarpentier, Y., CLAES, V. A., Vallée, A., & Hébert, J. (2017) · PPAR Research · doi:10.1155/2017/5879090 · Cited by 99 · see citing works
Preeclampsia: novel insights from global RNA profiling of trophoblast subpopulations
Gormley, M. J., Ona, K. R., Kapidzic, M., Garrido‐Gómez, T., Zdravkovic, T., & Fisher, S. J. (2017) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2017.03.017 · Cited by 95 · see citing works
Molecular Mechanisms of Lipid-Based Metabolic Adaptation Strategies in Response to Cold
Wu, G., Baumeister, R., & Heimbucher, T. (2023) · Cells · doi:10.3390/cells12101353 · Cited by 96 · see citing works
Pavan, M., Menin, S., Bassani, D., Sturlese, M., & Moro, S. (2022) · Journal of Chemical Information and Modeling · doi:10.1021/acs.jcim.2c00995 · Cited by 93 · see citing works
Pathophysiological role of metabolic flexibility on metabolic health
Galgani, J. E., & Fernández‐Verdejo, R. (2020) · Obesity Reviews · doi:10.1111/obr.13131 · Cited by 90 · see citing works
Warburg effect hypothesis in autism Spectrum disorders
Vallée, A., & Vallée, J.-N. (2018) · Molecular Brain · doi:10.1186/s13041-017-0343-6 · Cited by 91 · see citing works
Rajeshkumar, N. V., Yabuuchi, S., Pai, S. G., Oliveira, E. D., Kamphorst, J. J., Rabinowitz, J. D., Tejero, H., Al‐Shahrour, F., Hidalgo, M. M., Maitra, A., et al. (2017) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-17-1115 · Cited by 90 · see citing works
Zhang, S., Hu, X., Zhang, W., Yao, H., & Tam, K. Y. (2015) · Drug Discovery Today · doi:10.1016/j.drudis.2015.03.012 · Cited by 89 · see citing works
Self-citationLi, G., Li, M., Hu, J., Lei, R., Xiong, H., Ji, H., Yin, H., Wei, Q., & Hu, G. (2016) · Oncogene · doi:10.1038/onc.2016.265 · Cited by 89 · see citing works
Mitochondrial Function in Muscle Stem Cell Fates
Bhattacharya, D., & Scimè, A. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00480 · Cited by 88 · see citing works
Guglielmetti, C., Najac, C., Didonna, A., der Linden, A. V., Ronen, S. M., & Chaumeil, M. M. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1613345114 · Cited by 83 · see citing works
Forteza, M. J., Berg, M., Edsfeldt, A., Sun, J., Baumgartner, R., Kareinen, I., Casagrande, F. B., Hedin, U., Zhang, S., Vučković, I., et al. (2023) · Cardiovascular Research · doi:10.1093/cvr/cvad038 · Cited by 84 · see citing works
Self-citationShi, G., & McQuibban, G. A. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.01.029 · Cited by 82 · see citing works
Lung dendritic-cell metabolism underlies susceptibility to viral infection in diabetes
Nobs, S. P., Kolodziejczyk, A. A., Adler, L. N., Horesh, N., Botscharnikow, C., Herzog, E., Mohapatra, G., Hejndorf, S., Hodgetts, R. J., Spivak, I., et al. (2023) · Nature · doi:10.1038/s41586-023-06803-0 · Cited by 86 · see citing works
Pyrimidines maintain mitochondrial pyruvate oxidation to support de novo lipogenesis
Sahu, U., Villa, E., Reczek, C. R., Zhao, Z., O’Hara, B. P., Torno, M. D., Mishra, R., Shannon, W. D., Asara, J. M., Gao, P., et al. (2024) · Science · doi:10.1126/science.adh2771 · Cited by 82 · see citing works
Casciano, J. C., Perry, C. E., Cohen-Nowak, A. J., Miller, K. D., Voorde, J. V., Zhang, Q., Chalmers, S., Sandison, M. E., Liu, Q., Hedley, A., et al. (2020) · British Journal of Cancer · doi:10.1038/s41416-019-0711-3 · Cited by 80 · see citing works
Lecarpentier, Y., CLAES, V. A., Vallée, A., & Hébert, J. (2017) · Clinical and Translational Medicine · doi:10.1186/s40169-017-0144-7 · Cited by 75 · see citing works
The Importance of Mitochondrial Pyruvate Carrier in Cancer Cell Metabolism and Tumorigenesis
Ruiz-Iglesias, A., & Mañes, S. (2021) · Cancers · doi:10.3390/cancers13071488 · Cited by 76 · see citing works
Mitochondrial Dysfunction in Cancer Cachexia: Impact on Muscle Health and Regeneration
Beltrà, M., Pin, F., Ballarò, R., Costelli, P., & Penna, F. (2021) · Cells · doi:10.3390/cells10113150 · Cited by 76 · see citing works
Metabolic Flexibility and Its Impact on Health Outcomes
Palmer, B. F., & Clegg, D. J. (2022) · Mayo Clinic Proceedings · doi:10.1016/j.mayocp.2022.01.012 · Cited by 77 · see citing works
Metabolic Features of Multiple Myeloma
Arfani, C. E., Veirman, K. D., Maes, K., Bruyne, E. D., & Menu, E. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19041200 · Cited by 75 · see citing works
STAT3‐dependent analysis reveals PDK4 as independent predictor of recurrence in prostate cancer
Oberhuber, M., Pecoraro, M., Rusz, M., Oberhuber, G., Wieselberg, M., Haslinger, P., Gurnhofer, E., Schlederer, M., Limberger, T., Lagger, S., et al. (2020) · Molecular Systems Biology · doi:10.15252/msb.20199247 · Cited by 70 · see citing works
Fekir, K., Dubois‐Pot‐Schneider, H., Désert, R., Daniel, Y., Glaise, D., Rauch, C., Morel, F., Fromenty, B., Musso, O. C., Cabillic, F., et al. (2019) · Cancer Research · doi:10.1158/0008-5472.can-18-2110 · Cited by 73 · see citing works
Inositol Hexakisphosphate Kinase 3 Regulates Metabolism and Lifespan in Mice
Moritoh, Y., Oka, M., Yasuhara, Y., Hozumi, H., Iwachidow, K., Fuse, H., & Tozawa, R. (2016) · Scientific Reports · doi:10.1038/srep32072 · Cited by 70 · see citing works
Eblimit, Z., Thevananther, S., Karpen, S. J., Taegtmeyer, H., Moore, D. D., Adorini, L., Penny, D. J., & Desai, M. S. (2018) · Cardiovascular Therapeutics · doi:10.1111/1755-5922.12462 · Cited by 72 · see citing works
Nayak, M. K., Dhanesha, N., Doddapattar, P., Rodriguez, O., Sonkar, V. K., Dayal, S., & Chauhan, A. K. (2018) · Blood Advances · doi:10.1182/bloodadvances.2018022392 · Cited by 71 · see citing works
Kim, M., Sinam, I. S., Zerwa, S., Jeon, J., & Lee, I. (2023) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2022.0305 · Cited by 68 · see citing works
The pyruvate dehydrogenase complex: Life’s essential, vulnerable and druggable energy homeostat
Stacpoole, P. W., & McCall, C. E. (2023) · Mitochondrion · doi:10.1016/j.mito.2023.02.007 · Cited by 68 · see citing works
Xu, W., Billon, C., Li, H., Wilderman, A. S., Qi, L., Graves, A., Rideb, J. R. D. C., Zhao, Y., Hayes, M. E., Yu, K., et al. (2023) · Circulation · doi:10.1161/circulationaha.123.066542 · Cited by 67 · see citing works
Reiter, R. J., Sharma, R., & Rosales‐Corral, S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22020764 · Cited by 68 · see citing works
Vallée, A., Lecarpentier, Y., Guillevin, R., & Vallée, J.-N. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00352 · Cited by 66 · see citing works
Liang, X., Yee, S. W., Chien, H., Chen, E. C., Luo, Q., Zou, L., Piao, M., Mifune, A., Chen, L., Calvert, M., et al. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2002907 · Cited by 63 · see citing works
Nox4 mediates skeletal muscle metabolic responses to exercise
Specht, K. S., Kant, S., Addington, A. K., McMillan, R. P., Hulver, M. W., Learnard, H., Campbell, M., Donnelly, S. R., Caliz, A. D., Pei, Y., et al. (2021) · Molecular Metabolism · doi:10.1016/j.molmet.2020.101160 · Cited by 64 · see citing works
Self-citationEmpagliflozin reduces podocyte lipotoxicity in experimental Alport syndrome
Ge, M., Molina, J., Kim, J., Mallela, S. K., Ahmad, A., Santos, J. V., Al‐Ali, H., Mitrofanova, A. V., Sharma, K., Fontanesi, F., et al. (2023) · eLife · doi:10.7554/elife.83353 · Cited by 63 · see citing works
Hao, X., Gu, H., Chen, C.-Q., Huang, D., Zhao, Y.-Z., Xie, L., Zou, Y.-J., Shu, H. S., Zhang, Y., He, X.-X., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2018.11.013 · Cited by 57 · see citing works
miR-182 Regulates Metabolic Homeostasis by Modulating Glucose Utilization in Muscle
Zhang, D., Li, Y., Yao, X., Wang, H. J., Zhao, L., Jiang, H., Yao, X., Zhang, S., Cheng, Y., Liu, W., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.06.040 · Cited by 62 · see citing works
Self-citationPlasma Lactate as a Marker for Metabolic Health
Broskey, N. T., Zou, K., Dohm, G. L., & Houmard, J. A. (2020) · Exercise and Sport Sciences Reviews · doi:10.1249/jes.0000000000000220 · Cited by 61 · see citing works
Shannon, C. E., Ragavan, M., Palavicini, J. P., Fourcaudot, M. J., Bakewell, T. M., Valdez, I., Ayala, I., Jin, E. S., Madesh, M., Han, X., et al. (2020) · Molecular Metabolism · doi:10.1016/j.molmet.2020.101154 · Cited by 61 · see citing works
Jeon, J., Thoudam, T., Choi, E. J., Kim, M., Harris, R. A., & Lee, I. (2020) · Journal of Diabetes Investigation · doi:10.1111/jdi.13345 · Cited by 60 · see citing works
Aerobic glycolysis in amyotrophic lateral sclerosis and Huntington’s disease
Vallée, A., Lecarpentier, Y., Guillevin, R., & Vallée, J.-N. (2018) · Reviews in the Neurosciences · doi:10.1515/revneuro-2017-0075 · Cited by 58 · see citing works
Glucose metabolism: A link between traumatic brain injury and Alzheimer’s disease
Xu, X., Yang, M.-S., Zhang, B., Niu, F., Dong, J., & Liu, B. (2020) · Chinese Journal of Traumatology · doi:10.1016/j.cjtee.2020.10.001 · Cited by 59 · see citing works
Xu, S., Guo, J., & Zhang, W. (2019) · Journal of Cellular Biochemistry · doi:10.1002/jcb.28552 · Cited by 57 · see citing works
The OGT–c-Myc–PDK2 axis rewires the TCA cycle and promotes colorectal tumor growth
Wang, H., Sun, J., Sun, H., Wang, Y., Lin, B., Wu, L., Qin, W., Zhu, Q., & Yi, W. (2024) · Cell Death and Differentiation · doi:10.1038/s41418-024-01315-4 · Cited by 60 · see citing works
Wu, Y., Wu, S., & Wei, Y. (2014) · Free Radical Research · doi:10.3109/10715762.2014.920956 · Cited by 56 · see citing works
Engineering protein A affinity chromatography.
Jungbauer, A., & Hahn, R. (2004) · PubMed · Cited by 56 · see citing works
Empagliflozin protects mice against diet-induced obesity, insulin resistance and hepatic steatosis
Radlinger, B., Ress, C., Folie, S., Salzmann, K., Lechuga, A., Weiss, B., Salvenmoser, W., Graber, M., Hirsch, J., Holfeld, J., et al. (2022) · Diabetologia · doi:10.1007/s00125-022-05851-x · Cited by 58 · see citing works
Endoplasmic reticulum stress-induced complex I defect: Central role of calcium overload
Mohsin, A. A., Thompson, J., Hu, Y., Hollander, J. M., Lesnefsky, E. J., & Chen, Q. (2020) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2020.108299 · Cited by 54 · see citing works
Sheeran, F. L., Angerosa, J., Liaw, N. Y., Cheung, M. M. H., & Pepe, S. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/4532592 · Cited by 53 · see citing works
Škugor, A., Kjos, N. P., Sundaram, A. Y. M., Mydland, L. T., Ånestad, R. M., Tauson, A., & Øverland, M. (2019) · PLoS ONE · doi:10.1371/journal.pone.0220441 · Cited by 52 · see citing works
Salt-inducible Kinase 3 Signaling Is Important for the Gluconeogenic Programs in Mouse Hepatocytes
Itoh, Y., Sanosaka, M., Fuchino, H., Yahara, Y., Kumagai, A., Takemoto, D., Kagawa, M., Doi, J., Ohta, M., Tsumaki, N., et al. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.640821 · Cited by 52 · see citing works
Vallée, A., Lecarpentier, Y., Guillevin, R., & Vallée, J.-N. (2018) · NeuroMolecular Medicine · doi:10.1007/s12017-018-8486-x · Cited by 52 · see citing works
Beneficial Effects of Acetyl-DL-Leucine (ADLL) in a Mouse Model of Sandhoff Disease
Kaya, E., Smith, D. A., Smith, C., Boland, B., Strupp, M. L., & Platt, F. M. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9041050 · Cited by 52 · see citing works
Lysosome-Dependent LXR and PPARδ Activation Upon Efferocytosis in Human Macrophages
Mota, A. C., Dominguez, M., Weigert, A., Snodgrass, R. G., Namgaladze, D., & Brüne, B. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.637778 · Cited by 51 · see citing works
Low Levels of Lipopolysaccharide Modulate Mitochondrial Oxygen Consumption in Skeletal Muscle
Frisard, M. I., Wu, Y., McMillan, R. P., Voelker, K. A., Wahlberg, K. A., Anderson, A. S., Boutagy, N. E., Resendes, K., Ravussin, É., & Hulver, M. W. (2014) · Metabolism · doi:10.1016/j.metabol.2014.11.007 · Cited by 49 · see citing works
Self-citationCunha‐Oliveira, T., Ferreira, L. L., Coelho, A. R., Deus, C. M., & Oliveira, P. J. (2018) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2018.04.009 · Cited by 49 · see citing works
Elements of the cellular metabolic structure
la Fuente, I. M. D. (2015) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2015.00016 · Cited by 48 · see citing works
Asaikkutti, A., Bhavan, P. S., & Vimala, K. (2016) · Aquaculture · doi:10.1016/j.aquaculture.2016.06.014 · Cited by 49 · see citing works
Differing roles of pyruvate dehydrogenase kinases during mouse oocyte maturation
Hou, X., Zhang, L., Han, L., Ge, J., Ma, R., Zhang, X., Moley, K. H., Schedl, T., & Wang, Q. (2015) · Journal of Cell Science · doi:10.1242/jcs.167049 · Cited by 49 · see citing works
Wu, C., Tso, S.-C., Chuang, J. L., Gui, W. J., Lou, M., Sharma, G., Khemtong, C., Qi, X., Wynn, R., & Chuang, D. (2018) · Molecular Metabolism · doi:10.1016/j.molmet.2018.03.014 · Cited by 49 · see citing works
van Otterdijk, S. D., Binder, A. M., Szic, K. S. V., Schwald, J., & Michels, K. B. (2017) · PLoS ONE · doi:10.1371/journal.pone.0180955 · Cited by 48 · see citing works
Kleinert, M., Parker, B. L., Jensen, T. E., Raun, S. H., Pham, T. C. P., Han, X., James, D. E., Richter, E. A., & Sylow, L. (2018) · Scientific Reports · doi:10.1038/s41598-018-28540-5 · Cited by 46 · see citing works
Zhao, Y., Tran, M., Wang, L., Shin, D., & Wu, J. (2020) · Hepatology Communications · doi:10.1002/hep4.1484 · Cited by 47 · see citing works
Suárez‐Calvet, X., Fernández‐Simón, E., Benito, D. N., Jou, C., Piñol‐Jurado, P., Villalobos, E., Ortez, C., Monceau, A., Schiava, M., Codina, A., et al. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-06103-5 · Cited by 45 · see citing works
Han, X., Ma, W., Zhu, Y., Sun, X., & Liu, N. (2020) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2020.110878 · Cited by 45 · see citing works
Kesäniemi, J., Jernfors, T., Lavrinienko, A., Kivisaari, K., Kiljunen, M., Mappes, T., & Watts, P. C. (2019) · Molecular Ecology · doi:10.1111/mec.15241 · Cited by 44 · see citing works
Flora, G. D., Nayak, M. K., Ghatge, M., Kumskova, M., Patel, R. B., & Chauhan, A. K. (2023) · Blood Advances · doi:10.1182/bloodadvances.2023010100 · Cited by 43 · see citing works
Hypobaric hypoxia-driven energy metabolism disturbance facilitates vascular endothelial dysfunction
Zhang, Y., Wang, J., He, M., Liu, J., Zhao, J., He, J., Wang, C., Li, Y., Xiao, C., Fan, C., et al. (2025) · Redox Biology · doi:10.1016/j.redox.2025.103675 · Cited by 42 · see citing works
MicroRNA regulation and analytical methods in cancer cell metabolism
Zhang, L.-F., Jiang, S., & Liu, M. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2508-y · Cited by 40 · see citing works
Dissociation of Muscle Insulin Resistance from Alterations in Mitochondrial Substrate Preference
Song, J. D., Alves, T. C., Befroy, D. E., Perry, R. J., Mason, G. F., Zhang, X., Munk, A., Zhang, Y., Zhang, D., Cline, G. W., et al. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.09.008 · Cited by 40 · see citing works
Metastasis organotropism in colorectal cancer: advancing toward innovative therapies
He, K., Wang, Z., Luo, M., Li, B., Ding, N., Li, L., He, B., Wang, H., Cao, J., Huang, C., et al. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04460-5 · Cited by 42 · see citing works
Type 3 diabetes and metabolic reprogramming of brain neurons: causes and therapeutic strategies
Meng, X., Zhang, H., Zhao, Z., Li, S., Zhang, X., Guo, R., Li, H., Yuan, Y., Li, W., Song, Q., et al. (2025) · Molecular Medicine · doi:10.1186/s10020-025-01101-z · Cited by 43 · see citing works
Mechanisms of Vascular Calcification: The Pivotal Role of Pyruvate Dehydrogenase Kinase 4
Leem, J., & Lee, I. K. (2016) · Endocrinology and Metabolism · doi:10.3803/enm.2016.31.1.52 · Cited by 40 · see citing works
LETM1 couples mitochondrial DNA metabolism and nutrient preference
Durigon, R., Mitchell, A., Jones, A. W. E., Manole, A., Mennuni, M., Hirst, E. M. A., Houlden, H., Maragni, G., Lattante, S., Doronzio, P. N., et al. (2018) · EMBO Molecular Medicine · doi:10.15252/emmm.201708550 · Cited by 41 · see citing works
- Authors
- Zhang, S., Hulver, M. W., McMillan, R. P., Cline, M. A., & Gilbert, E. R.
- Affiliations
- Virginia Tech (US)
- Corresponding author
- Gilbert, Elizabeth R
- Venue
- Nutrition & Metabolism
- Published
- 2014-02-12
- Volume
- 11
- Issue
- 1
- Pages
- 10-10
- ISSN
- 1743-7075 (ISSN-L)
- PMC
- PMC3925357
- OpenAlex
- W2170096200
- Cited by
- 450
- References
- 78
- Citations by year
- 2026: 19 · 2025: 43 · 2024: 34 · 2023: 70 · 2022: 45 · 2021: 39 · 2020: 55 · 2019: 38 · 2018: 40 · 2017: 23 · 2016: 20 · 2015: 18 · 2014: 5
- FWCI
- 9.79
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Nutrition & Metabolism (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- VTechWorks (Virginia Tech) (submittedVersion, cc-by)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Biochemical Acid Research Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Keywords
- pyruvate dehydrogenase kinase, pyruvate dehydrogenase complex, metabolic flexibility, PDK4, energy homeostasis, glucose oxidation, fatty acid oxidation, substrate competition, metabolic inflexibility, type 2 diabetes, metabolic disorders
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