The multifaceted pyruvate metabolism: role of the mitochondrial pyruvate carrier
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Pyruvate, the end product of glycolysis, plays a major role in cell metabolism. Produced in the cytosol, it is oxidized in the mitochondria where it fuels the citric acid cycle and boosts oxidative phosphorylation. Its sole entry point into mitochondria is through the recently identified mitochondrial pyruvate carrier (MPC). In this review, we report the latest findings on the physiology of the MPC and we discuss how a dysfunctional MPC can lead to diverse pathologies, including neurodegenerative diseases, metabolic disorders, and cancer.
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Genetic or pharmacological inhibition of the MPC in the brain affects diverse brain activities.
“Genetic or pharmacological inhibition of the MPC in the brain has been shown to affect diverse brain activities (Buchanan and Taylor, 2020; Zangari et al., 2020).”
From Inhibition of the mitochondrial pyruvate carrier in astrocytes reduces amyloid and tau accumulation in the 3xTgAD mouse model of Alzheimer's disease (2024) · cites this paper as Zangari et al., 2020
Section 4.1 reports several effects of pharmacological MPC inhibition relevant to the brain, including neuronal protection and increased glucose uptake in affected brain regions. It does not establish comparable effects from genetic inhibition in the brain; instead, it calls for neuron- or glia-specific genetic studies to confirm the drug findings. (LLM, conf=0.88)
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Cites
Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation
Vander Heiden, M. G., Cantley, L. C., & Thompson, C. B. (2009) · Science · doi:10.1126/science.1160809 · Cited by 16,197 · see citing works
On Respiratory Impairment in Cancer Cells
Warburg, O. H. (1956) · Science · doi:10.1126/science.124.3215.269 · Cited by 3,472 · see citing works
Brain energy metabolism: focus on Astrocyte-neuron metabolic cooperation
Bélanger, M., Allaman, I., & Magistretti, P. J. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.08.016 · Cited by 2,313 · see citing works
Skeletal Muscle Insulin Resistance Is the Primary Defect in Type 2 Diabetes
DeFronzo, R. A., & Tripathy, D. (2009) · Diabetes Care · doi:10.2337/dc09-s302 · Cited by 2,102 · see citing works
Oxidative stress, dysfunctional glucose metabolism and Alzheimer disease
Butterfield, D. A., & Halliwell, B. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0132-6 · Cited by 1,954 · see citing works
Glucose feeds the TCA cycle via circulating lactate
Hui, S., Ghergurovich, J. M., Morscher, R. J., Jang, C., Teng, X., Lu, W., Esparza, L. A., Reya, T., Zhan, L., Yanxiang Guo, J., et al. (2017) · Nature · doi:10.1038/nature24057 · Cited by 1,721 · see citing works
Lactate Metabolism in Human Lung Tumors
Faubert, B., Li, K. Y., Cai, L., Hensley, C. T., Kim, J., Zacharias, L. G., Yang, C., Do, Q. N., Doucette, S., Burguete, D., et al. (2017) · Cell · doi:10.1016/j.cell.2017.09.019 · Cited by 1,343 · see citing works
Regulation of hepatic glucose metabolism in health and disease
Petersen, M. C., Vatner, D. F., & Shulman, G. I. (2017) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2017.80 · Cited by 1,131 · see citing works
Tansey, M. G., & Goldberg, M. S. (2010) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.11.004 · Cited by 1,045 · see citing works
Energy metabolism of cancer: Glycolysis versus oxidative phosphorylation (Review)
Zheng, J. (2012) · Oncology Letters · doi:10.3892/ol.2012.928 · Cited by 953 · see citing works
Lactate in the Regulation of Tumor Microenvironment and Therapeutic Approaches
de la Cruz-López, K. G., Castro-Muñoz, L. J., Reyes-Hernández, D. O., García-Carrancá, A., & Manzo-Merino, J. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.01143 · Cited by 940 · see citing works
Athauda, D., Maclagan, K., Skene, S. S., Bajwa-Joseph, M., Letchford, D., Chowdhury, K., Hibbert, S., Budnik, N., Zampedri, L., Dickson, J., et al. (2017) · The Lancet · doi:10.1016/s0140-6736(17)31585-4 · Cited by 889 · see citing works
Bricker, D. K., Taylor, E. B., Schell, J. C., Orsak, T., Boutron, A., Chen, Y.-C., Cox, J. E., Cardon, C. M., Van Vranken, J. G., Dephoure, N., et al. (2012) · Science · doi:10.1126/science.1218099 · Cited by 843 · see citing works
Brain metabolism in health, aging, and neurodegeneration
Camandola, S., & Mattson, M. P. (2017) · The EMBO Journal · doi:10.15252/embj.201695810 · Cited by 752 · see citing works
Identification and Functional Expression of the Mitochondrial Pyruvate Carrier
Herzig, S., Raemy, E., Montessuit, S., Veuthey, J.-L., Zamboni, N., Westermann, B., Kunji, E. R. S., & Martinou, J.-C. (2012) · Science · doi:10.1126/science.1218530 · Cited by 747 · see citing works
Self-citationRegional aerobic glycolysis in the human brain
Vaishnavi, S. N., Vlassenko, A. G., Rundle, M. M., Snyder, A. Z., Mintun, M. A., & Raichle, M. E. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1010459107 · Cited by 738 · see citing works
Yang, C., Ko, B., Hensley, C. T., Jiang, L., Wasti, A. T., Kim, J., Sudderth, J., Calvaruso, M. A., Lumata, L., Mitsche, M., et al. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.09.025 · Cited by 679 · see citing works
Lopaschuk, G. D., & Jaswal, J. S. (2010) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0b013e3181e74a14 · Cited by 636 · see citing works
The androgen receptor fuels prostate cancer by regulating central metabolism and biosynthesis
Massie, C. E., Lynch, A., Ramos‐Montoya, A., Boren, J., Stark, R., Fazli, L., Warren, A., Scott, H., Madhu, B., Sharma, N., et al. (2011) · The EMBO Journal · doi:10.1038/emboj.2011.158 · Cited by 624 · see citing works
Insulin regulation of gluconeogenesis
Hatting, M., Tavares, C. D. J., Sharabi, K., Rines, A. K., & Puigserver, P. (2017) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13435 · Cited by 589 · see citing works
A Mitochondrial Switch Promotes Tumor Metastasis
Porporato, P. E., Payen, V. L., Pérez‐Escuredo, J., Saedeleer, C. J. D., Danhier, P., Copetti, T., Dhup, S., Tardy, M., Vazeille, T., Bouzin, C., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.06.043 · Cited by 571 · see citing works
Metabolic Signaling in Fuel-Induced Insulin Secretion
Prentki, M., Matschinsky, F. M., & Madiraju, S. R. M. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.05.018 · Cited by 548 · see citing works
Exenatide and the treatment of patients with Parkinson's disease
Aviles-Olmos, I., Dickson, J., Kefalopoulou, Z., Djamshidian, A., Ell, P., Soderlund, T., Whitton, P., Wyse, R., Isaacs, T., Lees, A., et al. (2013) · Journal of Clinical Investigation · doi:10.1172/jci68295 · Cited by 529 · see citing works
Schell, J. C., Olson, K. A., Jiang, L., Hawkins, A. J., Van Vranken, J. G., Xie, J., Egnatchik, R. A., Earl, E. G., DeBerardinis, R. J., & Rutter, J. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.09.026 · Cited by 363 · see citing works
Triggers, Facilitators, and Aggravators: Redefining Parkinson’s Disease Pathogenesis
Johnson, M., Stecher, B., Labrie, V., Brundin, L., & Brundin, P. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.09.007 · Cited by 312 · see citing works
Thiazolidinediones are acute, specific inhibitors of the mitochondrial pyruvate carrier
Divakaruni, A. S., Wiley, S. E., Rogers, G. W., Andreyev, A. Y., Petrosyan, S., Loviscach, M., Wall, E. A., Yadava, N., Heuck, A. P., Ferrick, D. A., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1303360110 · Cited by 308 · see citing works
Motor and Cognitive Advantages Persist 12 Months After Exenatide Exposure in Parkinson’s Disease
Avilés-Olmos, I., Dickson, J. C., Kefalopoulou, Z. M., Djamshidian, A., Kahan, J., Ell, P. J., Whitton, P. S., Wyse, R. K. H., Isaacs, T., Lees, A. J., et al. (2014) · Journal of Parkinson s Disease · doi:10.3233/jpd-140364 · Cited by 300 · see citing works
Metabolic cycling in control of glucose-stimulated insulin secretion.
Jensen, M., Joseph, J., Ronnebaum, S., Burgess, S. C., Sherry, A., & Newgard, C. (2008) · American Journal of Physiology. Endocrinology and Metabolism · doi:10.1152/ajpendo.90604.2008 · Cited by 282 · see citing works
Regulation of Substrate Utilization by the Mitochondrial Pyruvate Carrier
Vacanti, N. M., Divakaruni, A. S., Green, C. R., Parker, S. J., Henry, R. R., Ciaraldi, T. P., Murphy, A. N., & Metallo, C. M. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.09.024 · Cited by 277 · see citing works
Cappel, D. A., Deja, S., Duarte, J. A. G., Kucejova, B., Iñigo, M., Fletcher, J. A., Fu, X., Berglund, E. D., Liu, T., Elmquist, J. K., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.03.014 · Cited by 242 · see citing works
Gray, L. R., Sultana, M. R., Rauckhorst, A. J., Oonthonpan, L., Tompkins, S. C., Sharma, A., Fu, X., Miao, R., Pewa, A. D., Brown, K., et al. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.07.027 · Cited by 217 · see citing works
Harrison, S. A., Alkhouri, N., Davison, B. A., Sanyal, A., Edwards, C., Colca, J. R., Lee, B. H., Loomba, R., Cusi, K., Kolterman, O., et al. (2020) · Journal of Hepatology · doi:10.1016/j.jhep.2019.10.023 · Cited by 211 · see citing works
McCommis, K. S., Chen, Z., Fu, X., McDonald, W. G., Colca, J. R., Kletzien, R. F., Burgess, S. C., & Finck, B. N. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.07.028 · Cited by 210 · see citing works
Kim, J., Yu, L., Chen, W., Xu, Y., Wu, M., Todorova, D., Tang, Q., Feng, B., Jiang, L., Chen, G., et al. (2019) · Cancer Cell · doi:10.1016/j.ccell.2018.12.012 · Cited by 202 · see citing works
Ahmed, S. S. S. J., Santosh, W., Kumar, S., & Christlet, H. T. T. (2009) · Journal of Biomedical Science · doi:10.1186/1423-0127-16-63 · Cited by 197 · see citing works
Corbet, C., Bastien, E., Draoui, N., Doix, B., Mignion, L., Jordan, B. F., Marchand, A., Vanherck, J., Chaltin, P., Schakman, O., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03525-0 · Cited by 189 · see citing works
Yetkin-Arik, B., Vogels, I. M. C., Nowak-Sliwinska, P. M., Weiss, A., Houtkooper, R. H., Noorden, C. J. F. V., Klaassen, I., & Schlingemann, R. O. (2019) · Scientific Reports · doi:10.1038/s41598-019-48676-2 · Cited by 189 · see citing works
Ghosh, A., Tyson, T., George, S., Hildebrandt, E. N., Steiner, J. A., Madaj, Z., Schulz, E., Machiela, E., McDonald, W. G., Galvis, M. L. E., et al. (2016) · Science Translational Medicine · doi:10.1126/scitranslmed.aag2210 · Cited by 187 · see citing works
Jézégou, A., Llinares, E., Anne, C., Kieffer‐Jaquinod, S., O’Regan, S., Aupetit, J., Chabli, A., Sagné, C., Debacker, C., Chadefaux, B., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1211198109 · Cited by 179 · see citing works
Structure and function of SemiSWEET and SWEET sugar transporters
Feng, L., & Frommer, W. B. (2015) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2015.05.005 · Cited by 173 · see citing works
Regulation of Tumor Initiation by the Mitochondrial Pyruvate Carrier
Bensard, C., Wisidagama, D. R., Olson, K. A., Berg, J. A., Krah, N. M., Schell, J. C., Nowinski, S. M., Fogarty, S., Bott, A. J., Wei, P., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.11.002 · Cited by 170 · see citing works
Bader, D. A., Hartig, S. M., Putluri, V., Foley, C., Hamilton, M. P., Smith, E. A., Saha, P., Panigrahi, A., Walker, C. M., Zong, L., et al. (2018) · Nature Metabolism · doi:10.1038/s42255-018-0002-y · Cited by 168 · see citing works
The transport of pyruvate in rat liver mitochondria
Papa, S., Francavilla, A., Paradies, G., & Meduri, B. (1971) · FEBS Letters · doi:10.1016/0014-5793(71)80200-4 · Cited by 166 · see citing works
Inhibition of the mitochondrial pyruvate carrier protects from excitotoxic neuronal death
Divakaruni, A. S., Wallace, M., Buren, C., Martyniuk, K. M., Andreyev, A. Y., Li, E., Fields, J. A., Cordes, T., Reynolds, I. J., Bloodgood, B. L., et al. (2017) · The Journal of Cell Biology · doi:10.1083/jcb.201612067 · Cited by 157 · see citing works
Glucose metabolism in nerve terminals
Ashrafi, G., & Ryan, T. A. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.03.007 · Cited by 146 · see citing works
McCommis, K. S., Hodges, W. T., Brunt, E. M., Nalbantoglu, I., McDonald, W. G., Holley, C. L., Fujiwara, H., Schaffer, J. E., Colca, J. R., & Finck, B. N. (2016) · Hepatology · doi:10.1002/hep.29025 · Cited by 138 · see citing works
Regulation of mitochondrial pyruvate uptake by alternative pyruvate carrier complexes
Bender, T., Pena, G., & Martinou, J. (2015) · The EMBO Journal · doi:10.15252/embj.201490197 · Cited by 134 · see citing works
Self-citationBrauer, R., Bhaskaran, K., Chaturvedi, N., Dexter, D. T., Smeeth, L. L., & Douglas, I. (2015) · PLoS Medicine · doi:10.1371/journal.pmed.1001854 · Cited by 124 · see citing works
Rossi, A., Rigotto, G., Valente, G., Giorgio, V., Basso, E., Filadi, R., & Pizzo, P. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.01.060 · Cited by 109 · see citing works
Glitazone use associated with reduced risk of Parkinson's disease
Brakedal, B., Flønes, I. H., Reiter, S. F., Torkildsen, Ø., Dölle, C., Aßmus, J., Haugarvoll, K., & Tzoulis, C. (2017) · Movement Disorders · doi:10.1002/mds.27128 · Cited by 108 · see citing works
Vigueira, P. A., McCommis, K. S., Schweitzer, G. G., Remedi, M. S., Chambers, K. T., Fu, X., McDonald, W. G., Cole, S. L., Colca, J. R., Kletzien, R. F., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.05.017 · Cited by 101 · see citing works
Loss of MPC1 reprograms retinal metabolism to impair visual function
Grenell, A., Wang, Y., Yam, M., Swarup, A., Dilan, T. L., Hauer, A., Linton, J. D., Philp, N. J., Gregor, E., Zhu, S., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1812941116 · Cited by 101 · see citing works
Patterson, J. N., Cousteils, K., Lou, J. W., Manning Fox, J. E., MacDonald, P. E., & Joseph, J. W. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.521666 · Cited by 98 · see citing works
Engrailed homeoprotein blocks degeneration in adult dopaminergic neurons through LINE‐1 repression
de Thé, F.-X. B., Rekaik, H., Pezé-Heidsieck, E., Massiani-Beaudoin, O., Joshi, R. L., Fuchs, J., & Prochiantz, A. (2018) · The EMBO Journal · doi:10.15252/embj.201797374 · Cited by 95 · see citing works
Compan, V., Pierredon, S., Vanderperre, B., Krznar, P., Marchiq, I., Zamboni, N., Pouysségur, J., & Martinou, J. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.06.035 · Cited by 92 · see citing works
Self-citationImpaired mitochondrial pyruvate importation in a patient and a fetus at risk
Brivet, M. (2003) · Molecular Genetics and Metabolism · doi:10.1016/s1096-7192(03)00016-7 · Cited by 92 · see citing works
Zhong, Y., Li, X., Yu, D., Li, X., Li, Y., Long, Y., Yuan, Y., Ji, Z., Zhang, M., Wen, J., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.5386 · Cited by 81 · see citing works
Tompkins, S. C., Sheldon, R. D., Rauckhorst, A. J., Noterman, M. F., Solst, S. R., Buchanan, J. L., Mapuskar, K. A., Pewa, A. D., Gray, L. R., Oonthonpan, L., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.07.098 · Cited by 79 · see citing works
Li, D., Wang, C., Ma, P., Yu, Q., Gu, M., Dong, L., Jiang, W., Pan, S., Xie, C., Han, J., et al. (2018) · Cell Death and Disease · doi:10.1038/s41419-018-0494-0 · Cited by 77 · see citing works
What Effects Might Exenatide have on Non-Motor Symptoms in Parkinson’s Disease: A Post Hoc Analysis
Athauda, D. S., Maclagan, K., Budnik, N., Zampedri, L., Hibbert, S., Skene, S. S., Chowdhury, K., Avilés-Olmos, I., Limousin, P. D., & Foltynie, T. (2018) · Journal of Parkinson s Disease · doi:10.3233/jpd-181329 · Cited by 77 · see citing works
Rauckhorst, A. J., Gray, L. R., Sheldon, R. D., Fu, X., Pewa, A. D., Feddersen, C. R., Dupuy, A. J., Gibson-Corley, K. N., Cox, J. E., Burgess, S. C., et al. (2017) · Molecular Metabolism · doi:10.1016/j.molmet.2017.09.002 · Cited by 74 · see citing works
The yeast mitochondrial pyruvate carrier is a hetero-dimer in its functional state
Tavoulari, S., Thangaratnarajah, C., Mavridou, V., Harbour, M. E., Martinou, J., & Kunji, E. R. (2019) · The EMBO Journal · doi:10.15252/embj.2018100785 · Cited by 73 · see citing works
Self-citationLi, X., Han, G., Li, X., Kan, Q., Fan, Z., Li, Y., Ji, Y., Zhao, J., Zhang, M., Grigalavicius, M., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.18199 · Cited by 71 · see citing works
Mitochondrial pyruvate and fatty acid flux modulate MICU1-dependent control of MCU activity
Nemani, N., Dong, Z., Daw, C. C., Madaris, T. R., Karthik, R., Enslow, B. T., Rubannelsonkumar, C. S., Shanmughapriya, S., Mallireddigari, V., Maity, S., et al. (2020) · Science Signaling · doi:10.1126/scisignal.aaz6206 · Cited by 71 · see citing works
Bioenergetics failure in neurodegenerative diseases: back to the future
Saxena, U. (2012) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.2012.664135 · Cited by 67 · see citing works
Sharma, A., Oonthonpan, L., Sheldon, R. D., Rauckhorst, A. J., Zhu, Z., Tompkins, S. C., Cho, K., Grzesik, W. J., Gray, L. R., Scerbo, D. A., et al. (2019) · eLife · doi:10.7554/elife.45873 · Cited by 67 · see citing works
Vanderperre, B., Herzig, S., Krznar, P., Hörl, M., Ammar, Z., Montessuit, S., Pierredon, S., Zamboni, N., & Martinou, J. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006056 · Cited by 63 · see citing works
Self-citationDecreased Mitochondrial Pyruvate Transport Activity in the Diabetic Heart
Vadvalkar, S. S., Matsuzaki, S., Eyster, C. A., Giorgione, J. R., Bockus, L. B., Kinter, C. S., Kinter, M. T., & Humphries, K. M. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.753509 · Cited by 63 · see citing works
Cao, T., Liccardo, D., LaCanna, R., Zhang, X., Lü, R., Finck, B. N., Leigh, T., Chen, X., Drosatos, K., & Tian, Y. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00042 · Cited by 60 · see citing works
Sugden, M. C., & Holness, M. J. (2011) · Islets · doi:10.4161/isl.3.6.17806 · Cited by 58 · see citing works
MPC1, a key gene in cancer metabolism, is regulated by COUPTFII in human prostate cancer
Wang, L., Xu, M., Qin, J., Lin, S., Lee, H.-J., Tsai, S. Y., & Tsai, M. (2016) · Oncotarget · doi:10.18632/oncotarget.7405 · Cited by 58 · see citing works
Shah, R. C., Matthews, D. C., Andrews, R. D., Capuano, A. W., Fleischman, D. A., VanderLugt, J. T., & Colca, J. R. (2014) · Current Alzheimer Research · doi:10.2174/1567205011666140616113406 · Cited by 57 · see citing works
Sirt3 binds to and deacetylates mitochondrial pyruvate carrier 1 to enhance its activity
Liang, L., Li, Q., Huang, L., Li, D., & Li, X. (2015) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2015.11.036 · Cited by 56 · see citing works
Cui, J., Quan, M., Xie, D., Gao, Y., Guha, S., Fallon, M. B., Chen, J., & Xie, K. (2020) · Oncogene · doi:10.1038/s41388-019-1051-8 · Cited by 55 · see citing works
Human mitochondrial pyruvate carrier 2 as an autonomous membrane transporter
Nagampalli, R. S. K., Quesñay, J. E. N., Adamóski, D., Islam, Z., Birch, J., Sebinelli, H. G., Girard, R. M. B. M., Ascenção, C. F. R., Fala, A. M., Pauletti, B. A., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-21740-z · Cited by 53 · see citing works
Timón‐Gómez, A., Proft, M., & Pascual‐Ahuir, A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0079405 · Cited by 51 · see citing works
Bowman, C. E., Zhao, L., Härtung, T., & Wolfgang, M. J. (2016) · Molecular and Cellular Biology · doi:10.1128/mcb.00166-16 · Cited by 51 · see citing works
Takaoka, Y., Konno, M., Koseki, J., Colvin, H. S., Asai, A., Tamari, K., Satoh, T., Mori, M., Doki, Y., Ogawa, K., et al. (2019) · Cancer Science · doi:10.1111/cas.13980 · Cited by 49 · see citing works
Vanderperre, B., Cermakova, K., Escoffier, J., Kaba, M., Bender, T., Nef, S., & Martinou, J. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.733840 · Cited by 48 · see citing works
Self-citationPark, S. H., Safi, R., Liu, X., Baldi, R. M., Liu, W., Liu, J., Locasale, J. W., Chang, C., & McDonnell, D. P. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.05.066 · Cited by 48 · see citing works
MPC1 and MPC2 expressions are associated with favorable clinical outcomes in prostate cancer
Li, X., Ji, Y., Han, G., Li, X., Fan, Z., Li, Y., Zhong, Y., Cao, J., Zhao, J., Zhang, M., et al. (2016) · BMC Cancer · doi:10.1186/s12885-016-2941-6 · Cited by 46 · see citing works
An ancestral role for the mitochondrial pyruvate carrier in glucose-stimulated insulin secretion
McCommis, K. S., Hodges, W. T., Bricker, D. K., Wisidagama, D. R., Compan, V., Remedi, M. S., Thummel, C. S., & Finck, B. N. (2016) · Molecular Metabolism · doi:10.1016/j.molmet.2016.06.016 · Cited by 44 · see citing works
Gomkale, R., Cruz‐Zaragoza, L. D., Suppanz, I., Guiard, B., Montoya, J., Callegari, S., Pacheu‐Grau, D., Warscheid, B., & Rehling, P. (2020) · Current Biology · doi:10.1016/j.cub.2020.01.024 · Cited by 42 · see citing works
Li, Y., Li, X., Kan, Q., Zhang, M., Li, X., Xu, R., Wang, J., Yu, D., Goscinski, M. A., Wen, J., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.13717 · Cited by 41 · see citing works
Thiazolidinediones and Parkinson Disease: A Cohort Study
Connolly, J. G., Bykov, K., & Gagne, J. J. (2015) · American Journal of Epidemiology · doi:10.1093/aje/kwv109 · Cited by 39 · see citing works
Treating Hepatic Steatosis and Fibrosis by Modulating Mitochondrial Pyruvate Metabolism
McCommis, K. S., & Finck, B. N. (2019) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2018.09.017 · Cited by 39 · see citing works
Rampelt, H., Sučec, I., Bersch, B., Horten, P., Perschil, I., Martinou, J., van der Laan, M., Wiedemann, N., Schanda, P., & Pfanner, N. (2020) · BMC Biology · doi:10.1186/s12915-019-0733-6 · Cited by 37 · see citing works
Self-citationMPC1 is essential for PGC-1α-induced mitochondrial respiration and biogenesis
Koh, E., Kim, Y. K., Shin, D., & Kim, K. (2018) · Biochemical Journal · doi:10.1042/bcj20170967 · Cited by 36 · see citing works
Tang, X., Chen, Q., Li, Y., Wang, Y., Zou, H., Fu, W., Niu, Q., Pan, Q., Jiang, P., Xu, X., et al. (2018) · Laboratory Investigation · doi:10.1038/s41374-018-0138-0 · Cited by 36 · see citing works
MPC1 deletion is associated with poor prognosis and temozolomide resistance in glioblastoma
Chai, Y., Wang, C., Liu, W., Fan, Y., & Zhang, Y. (2019) · Journal of Neuro-Oncology · doi:10.1007/s11060-019-03226-8 · Cited by 35 · see citing works
MPC1 deficiency accelerates lung adenocarcinoma progression through the STAT3 pathway
Zou, H., Chen, Q., Zhang, A., Wang, S., Wu, H., Yuan, Y., Wang, S., Yu, J. H., Luo, M., Wen, X., et al. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1324-8 · Cited by 34 · see citing works
Oonthonpan, L., Rauckhorst, A. J., Gray, L. R., Boutron, A., & Taylor, E. B. (2019) · JCI Insight · doi:10.1172/jci.insight.126132 · Cited by 31 · see citing works
Han, P., Wang, Y., Zhan, H., Weng, W., Yu, X., Ge, N., Wang, W., Song, G., Yi, T., Li, S., et al. (2019) · Europe PMC (PubMed Central) · Cited by 30 · see citing works
Stark, H., Fichtner, M., König, R., Lorkowski, S., & Schuster, S. (2015) · Biochimie · doi:10.1016/j.biochi.2015.09.017 · Cited by 23 · see citing works
Li, X., Li, Y., Han, G., Li, X., Ji, Y., Fan, Z., Zhong, Y., Cao, J., Zhao, J., Goscinski, M. A., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.13210 · Cited by 23 · see citing works
Tai, Y., Cao, F., Li, M., Li, P., Xu, T., Wang, X., Yu, Y., Gu, B., Yu, X., Cai, X., et al. (2018) · Redox Biology · doi:10.1016/j.redox.2018.10.024 · Cited by 22 · see citing works
Mitochondrial pyruvate carrier modulates the epithelial-mesenchymal transition in cholangiocarcinoma
Ohashi, T., Eguchi, H., Kawamoto, K., Konno, M., Asai, A., Colvin, H. S., Ueda, Y., Takaoka, H., Iwagami, Y., Yamada, D., et al. (2017) · Oncology Reports · doi:10.3892/or.2017.6172 · Cited by 18 · see citing works
Medrano-Soto, A., Ghazi, F., Hendargo, K. J., Moreno‐Hagelsieb, G., Myers, S., & Saier, M. H. (2020) · PLoS ONE · doi:10.1371/journal.pone.0231085 · Cited by 18 · see citing works
Lee, J., Jin, Z., Lee, D., Yun, J.-H., & Lee, W. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21093403 · Cited by 18 · see citing works
MSDC-0160 and MSDC-0602 Binding with Human Mitochondrial Pyruvate Carrier (MPC) 1 and 2 Heterodimer
Phelix, C. F., Bourdon, A. K., Dugan, J. L., Villareal, G., & Perry, G. L. (2017) · International Journal of Knowledge Discovery in Bioinformatics · doi:10.4018/ijkdb.2017070103 · Cited by 8 · see citing works
Mitochondrial Pyruvate Carrier 1 and 2 Heterodimer, In Silico, Models of Plant and Human Complexes
Dugan, J. L., Bourdon, A. K., & Phelix, C. F. (2017) · International Journal of Knowledge Discovery in Bioinformatics · doi:10.4018/ijkdb.2017070102 · Cited by 7 · see citing works
Alzheimer's and Parkinson's Disease Novel Therapeutic Target
Bourdon, A. K., Villareal, G., Perry, G. L., & Phelix, C. F. (2017) · International Journal of Knowledge Discovery in Bioinformatics · doi:10.4018/ijkdb.2017070104 · Cited by 4 · see citing works
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Energy metabolism in health and diseases
Liu, H., Wang, S., Wang, J., Guo, X., Song, Y., Fu, K., Gao, Z., Liu, D., He, W., & Yang, L. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02141-x · Cited by 438 · see citing works
Valdebenito, S., Malik, S., Luu, R. H., Loudig, O. D., Mitchell, M. I., Okafo, G. N., Bhat, K., Prideaux, B., & Eugenín, E. A. (2021) · Scientific Reports · doi:10.1038/s41598-021-93775-8 · Cited by 120 · see citing works
Mitochondrial pyruvate metabolism regulates the activation of quiescent adult neural stem cells
Petrelli, F., Scandella, V., Montessuit, S., Zamboni, N., Martinou, J., & Knobloch, M. (2023) · Science Advances · doi:10.1126/sciadv.add5220 · Cited by 86 · see citing works
Self-citationEffects of Metabolism on Macrophage Polarization Under Different Disease Backgrounds
Sun, J., Xu, X.-H., & Jin, L. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.880286 · Cited by 79 · see citing works
Cancer cell metabolism: Rewiring the mitochondrial hub
Oliveira, G. L., Coelho, A. R., Marques, R., & Oliveira, P. J. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2020.166016 · Cited by 62 · see citing works
The mitochondrial pyruvate carrier at the crossroads of intermediary metabolism
Yiew, N. K. H., & Finck, B. N. (2022) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00074.2022 · Cited by 63 · see citing works
Duarte, I. F., Caio, J. M., Moedas, M. F., Rodrigues, L., Leandro, P., Rivera, I. A., & Silva, M. F. B. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03996-3 · Cited by 47 · see citing works
The FASTK family proteins fine-tune mitochondrial RNA processing
Ohkubo, A., Haute, L. V., Rudler, D. L., Stentenbach, M., Steiner, F. A., Rackham, O., Minczuk, M. A., Filipovska, A., & Martinou, J. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009873 · Cited by 42 · see citing works
Self-citationOmics and Male Infertility: Highlighting the Application of Transcriptomic Data
Omolaoye, T. S., Omolaoye, V. A., Kandasamy, R. K., Hachim, M. Y., & du Plessis, S. S. (2022) · Life · doi:10.3390/life12020280 · Cited by 42 · see citing works
Endres, J. L., Chaudhari, S. S., Zhang, X., Prahlad, J., Wang, S., Foley, L. A., Luca, S., Bose, J. L., Thomas, V. C., & Bayles, K. W. (2022) · mBio · doi:10.1128/mbio.02827-21 · Cited by 38 · see citing works
Dwivedi, S. K., Arachchige, D. L., Olowolagba, A. M., Mahmoud, M. E., Cunnien, J., Tucker, D. R., Fritz, D. R., Werner, T., Luck, R. L., & Liu, H. (2023) · Journal of Materials Chemistry B · doi:10.1039/d3tb00645j · Cited by 36 · see citing works
Transcriptome Analysis on Key Metabolic Pathways in Rhodotorula mucilaginosa Under Pb(II) Stress
Chen, T., Shi, Y., Peng, C., Tang, L., Chen, Y., Wang, T., Wang, Z., Wang, S., & Li, Z. (2022) · Applied and Environmental Microbiology · doi:10.1128/aem.02215-21 · Cited by 36 · see citing works
Soriano‐Baguet, L., Grusdat, M., Kurniawan, H., Benzarti, M., Binsfeld, C., Ewen, A., Longworth, J., Bonetti, L., Guerra, L., Franchina, D. G., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112153 · Cited by 33 · see citing works
Mangrulkar, S. V., Wankhede, N. L., Kale, M. B., Upaganlawar, A. B., Taksande, B. G., Umekar, M. J., Anwer, M. K., Dailah, H. G., Mohan, S., & Behl, T. (2023) · Neurotoxicity Research · doi:10.1007/s12640-023-00647-2 · Cited by 35 · see citing works
Ethyl pyruvate, a versatile protector in inflammation and autoimmunity
Koprivica, I., Djedović, N., Stojanović, I., & Miljković, D. M. (2022) · Inflammation Research · doi:10.1007/s00011-021-01529-z · Cited by 32 · see citing works
Structure of mitochondrial pyruvate carrier and its inhibition mechanism
Zheng, H., Zhang, J., Xu, Y., Fine, E. J., Suomivuori, C., Dror, R. O., & Feng, L. (2025) · Nature · doi:10.1038/s41586-025-08667-y · Cited by 33 · see citing works
Inorganic Phosphate as “Bioenergetic Messenger” Triggers M2‐Type Macrophage Polarization
Sun, X., Li, Z., Wang, X., He, J. H., & Wu, Y. (2024) · Advanced Science · doi:10.1002/advs.202306062 · Cited by 28 · see citing works
Targeting mitochondrial transporters and metabolic reprogramming for disease treatment
Anselme, M., He, H., Lai, C., Luo, W., & Zhong, S. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-06976-4 · Cited by 31 · see citing works
Ni, Q., Li, M., & Yu, S. (2022) · Technology in Cancer Research & Treatment · doi:10.1177/15330338221081219 · Cited by 27 · see citing works
Shi, J., Hu, M., Xia, Z., Zhang, J., Wang, Z., Li, L., & Zhao, Y. (2024) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2024.117048 · Cited by 27 · see citing works
Post-harvest precooling technology and fresh-keeping mechanism of fruits and vegetables: A review
Dai, O., Wang, Y., Li, M., Hong, W., Lei, X., Ye, Z., Pang, J., & Sun, Y. (2025) · Postharvest Biology and Technology · doi:10.1016/j.postharvbio.2025.113623 · Cited by 25 · see citing works
Baek, S., Kim, D., Song, D. H., Kim, H. B., Lee, S., Kim, J. H., Lee, J., Hong, Y. J., Park, C. G., & Han, D. K. (2022) · Biomaterials Research · doi:10.1186/s40824-022-00334-x · Cited by 25 · see citing works
The Metabolic Syndrome: An Overview and Proposed Mechanisms
Thomaz, F. S., John, O. D., Sinha, P., Shafie, S. R., & Worrall, S. (2024) · Obesities · doi:10.3390/obesities4030020 · Cited by 24 · see citing works
Frame, A. K., Robinson, J. W., Mahmoudzadeh, N. H., Tennessen, J. M., Simon, A. F., & Cumming, R. C. (2023) · Aging · doi:10.18632/aging.204565 · Cited by 22 · see citing works
Mallet, D., Goutaudier, R., Barbier, E., Carnicella, S., Colca, J. R., Fauvelle, F., & Boulet, S. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02962-9 · Cited by 21 · see citing works
PKM2 induces mitophagy through the AMPK-mTOR pathway promoting CSFV proliferation
Liu, X., Yan, Q., Liu, X., Wei, W., Zou, L., Zhao, F., Zeng, S., Yi, L., Ding, H., Zhao, M., et al. (2024) · Journal of Virology · doi:10.1128/jvi.01751-23 · Cited by 19 · see citing works
Linghu, T., Zhao, Y.-H., Wu, W., Gao, Y., Tian, J., & Qin, X. (2022) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2022.148578 · Cited by 19 · see citing works
MPC2 variants disrupt mitochondrial pyruvate metabolism and cause an early-onset mitochondriopathy
Pujol, C., Lebigot, É., Gaignard, P., Galaï, S., Kraoua, I., Bault, J., Dard, R., Youssef-Turki, I. B., Omar, S., Boutron, A., et al. (2022) · Brain · doi:10.1093/brain/awac444 · Cited by 22 · see citing works
Ceyzériat, K., Badina, A. M., Petrelli, F., Montessuit, S., Nicolaides, A., Millet, P., Savioz, A., Martinou, J.-C., & Tournier, B. B. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2024.106623 · Cited by 18 · see citing works
Self-citationStructural Insights into the Human Mitochondrial Pyruvate Carrier Complexes
Xu, L., Phelix, C. F., & Chen, L. Y. (2021) · Journal of Chemical Information and Modeling · doi:10.1021/acs.jcim.1c00879 · Cited by 18 · see citing works
Lauria, G., Curcio, R., Lunetti, P., Tiziani, S., Coppola, V., Dolce, V., Fiermonte, G., & Ahmed, A. (2023) · Cancers · doi:10.3390/cancers15020411 · Cited by 18 · see citing works
Structure of human mitochondrial pyruvate carrier MPC1 and MPC2 complex
Sun, Y., Wang, Y., Zheng, X., Li, D., Wang, R., Chen, B., Zhou, N., Ayala, A., Tu, B. P., & Qi, X. (2025) · Nature Communications · doi:10.1038/s41467-025-61939-z · Cited by 18 · see citing works
Sepsis: Evidence-based pathogenesis and treatment
Pravda, J. (2021) · World Journal of Critical Care Medicine · doi:10.5492/wjccm.v10.i4.66 · Cited by 17 · see citing works
Yuan, H., Xun, H., Wang, J., Wang, J., Yao, X., & Tang, F. (2024) · Molecules · doi:10.3390/molecules29102266 · Cited by 16 · see citing works
Negreiros, R. S., Lander, N. M., Chiurillo, M. Á., Vercesi, A. E., & Docampo, R. (2021) · mBio · doi:10.1128/mbio.00540-21 · Cited by 15 · see citing works
Beresewicz, M., Krupska, O., Bochomulski, P., Dudzik, D., Chęcińska, A., Hilgier, W., Barbas, C., Zabłocki, K., & Zabłocka, B. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22168504 · Cited by 14 · see citing works
Colca, J. R., & Finck, B. N. (2022) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2022.929328 · Cited by 16 · see citing works
Berberine regulates glucose metabolism in largemouth bass by modulating intestinal microbiota
Xia, Y. L., Yang, H.-C., Zhang, K., Tian, J., Li, Z., Yu, E., Li, H.-Y., Gong, W., Xie, W., Wang, G.-J., et al. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1147001 · Cited by 14 · see citing works
Zhao, D., Zhang, X., Jin, W., Huang, P., Wan, H., & He, Y. T. (2024) · Phytomedicine · doi:10.1016/j.phymed.2024.155881 · Cited by 15 · see citing works
Cendrowska‐Pinkosz, M., Ostrowska-Leśko, M., Ognik, K., Krauze, M., Juśkiewicz, J., Dąbrowska, A. M., Szponar, J., & Mańdziuk, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23126706 · Cited by 15 · see citing works
Hou, Y., He, Y., Wang, J., Zhou, Y., Ma, B., Li, X., Shi, L., & Zhang, Q. (2023) · Clinica Chimica Acta · doi:10.1016/j.cca.2023.117530 · Cited by 15 · see citing works
Liu, G., Bao, Y., Li, Y., Khan, J., & Xing, B. (2025) · Environmental Science & Technology · doi:10.1021/acs.est.5c10086 · Cited by 14 · see citing works
Cao, G., Yang, S., Wang, H., Zhang, R., Wu, Y., Liu, J., Qiu, K., Dong, Y., & Yue, M. (2023) · Animals · doi:10.3390/ani13132172 · Cited by 14 · see citing works
da Fonseca, A. M., Ispada, J., dos Santos, É. C., de Lima, C. B., da Silva, J. V. A., Paulson, E., Goszczynski, D. E., Goissis, M. D., Ross, P. J., & Milazzotto, M. P. (2023) · Scientific Reports · doi:10.1038/s41598-023-38686-6 · Cited by 13 · see citing works
Yang, X., Yin, M.-L., Zhu, Y., Zhao, S., & Xi, H. (2024) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2024.135489 · Cited by 14 · see citing works
Insulin sensitizers in 2023: lessons learned and new avenues for investigation
Colca, J. R., Tanis, S. P., Kletzien, R. F., & Finck, B. N. (2023) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2023.2263369 · Cited by 13 · see citing works
Findlay, S., Nair, R., Merrill, R. A., Kaiser, Z., Cajelot, A., Aryanpour, Z., Heath, J., St‐Louis, C., Papadopoli, D. J., Topisirović, I., et al. (2023) · Blood Advances · doi:10.1182/bloodadvances.2022008345 · Cited by 13 · see citing works
Laghezza, A., Cerchia, C., Genovese, M., Leuci, R., Pranzini, E., Santi, A., Brunetti, L., Piemontese, L., Tortorella, P., Biswas, A., et al. (2023) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.2c02093 · Cited by 12 · see citing works
Sajad, M., Zahoor, I., Rashid, F., Cerghet, M., Rattan, R., & Giri, S. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03546-x · Cited by 12 · see citing works
Metabolomic signature of sperm in men with obesity-associated asthenozoospermia
Hou, Y., Wang, J., Pan, M., Zhou, Y., Wang, Y., Chen, J., Zhong, M., Li, X., & Zhang, Q. (2024) · Journal of Assisted Reproduction and Genetics · doi:10.1007/s10815-024-03294-4 · Cited by 12 · see citing works
Santos, H. O., & Penha-Silva, N. (2025) · Nutrition · doi:10.1016/j.nut.2024.112617 · Cited by 11 · see citing works
Metabolic reprogramming tailors T cell immunity in sepsis
Xian, D., Chen, F., Liu, B., & Wang, L. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1679493 · Cited by 11 · see citing works
Anaplerotic filling in heart failure: a review of mechanism and potential therapeutics
Alhasan, K. A., King, M. A., Pattar, B. S. B., Lewis, I. A., Lopaschuk, G. D., & Greenway, S. C. (2024) · Cardiovascular Research · doi:10.1093/cvr/cvae248 · Cited by 11 · see citing works
Farahani, A., Farahani, A., Kashfi, K., & Ghasemi, A. (2025) · Medical Gas Research · doi:10.4103/mgr.medgasres-d-24-00100 · Cited by 12 · see citing works
Mitochondrial metabolism of the facultative parasite Chilodonella uncinata (Alveolata, Ciliophora)
Bu, X., Zhao, W., Li, W., Zou, H., Wu, S., Li, M., & Wang, G. (2023) · Parasites & Vectors · doi:10.1186/s13071-023-05695-3 · Cited by 11 · see citing works
Hossain, M. I., Lee, J. H., Gagné, J., Khan, J., Poirier, G. G., King, P. H., Dawson, V. L., Dawson, T. M., & Andrabi, S. A. (2024) · The FASEB Journal · doi:10.1096/fj.202302559r · Cited by 11 · see citing works
(2021) · Biointerface Research in Applied Chemistry · doi:10.33263/briac115.1345313464 · Cited by 11 · see citing works
Enhancing vitamin B 5 biosynthesis by multimodule optimization and protein engineering
Zhang, B., Xiao, Y., Zhu, Y., Liu, C., Zhu, L., Zhou, J., Cai, X., Qian, G., Liu, Z., & Zheng, Y. (2025) · Green Chemistry · doi:10.1039/d5gc02458g · Cited by 10 · see citing works
Mitochondrial Dynamics during Development
Maheshwari, A., He, L., & Tronstad, K. J. (2023) · Newborn · doi:10.5005/jp-journals-11002-0053 · Cited by 10 · see citing works
Zhang, Y., Ding, N., Cao, J., Zhang, J., Liu, J., Zhang, C., & Jiang, L. (2024) · Journal of Proteome Research · doi:10.1021/acs.jproteome.4c00060 · Cited by 10 · see citing works
Hyperpolarised 13C-MRI using 13C-pyruvate in breast cancer: A review
Arponen, O., Wodtke, P., Gallagher, F. A., & Woitek, R. (2023) · European Journal of Radiology · doi:10.1016/j.ejrad.2023.111058 · Cited by 11 · see citing works
Wen, Z., Liu, Z., Bu, H., Liu, Y., Zhu, J., Hu, F., Li, Z., Huang, B., & Peng, F. (2024) · Fungal Biology · doi:10.1016/j.funbio.2024.08.005 · Cited by 9 · see citing works
Wang, X., Zhou, S., Dong, J., Wei, Z., Liu, Y., Huang, Y., Sui, J., & Zhu, L. (2025) · Aquatic Toxicology · doi:10.1016/j.aquatox.2025.107259 · Cited by 9 · see citing works
Yoon, K., Choi, Y., Keum, G. B., Yeom, S., Kim, S.-S., Kim, E. S., Park, H. J., Kim, J.-E., Park, J., Song, B., et al. (2024) · BMC Microbiology · doi:10.1186/s12866-024-03536-6 · Cited by 8 · see citing works
Fu, J., Chen, S., Tan, Y., Zou, K., Yu, X., Ji, L., Zhang, J., Xiao, X., Wang, W., Zhao, K., et al. (2024) · Journal of Environmental Management · doi:10.1016/j.jenvman.2024.123601 · Cited by 8 · see citing works
Metabolic Targets in CRC: The Emerging Role of Cytochrome P450 Inhibitors
Alshakarchi, H. I., Azari, H., Jeddoa, Z. M. A., Jafar, N. N. A., Khazaei, Y., Gataa, I. S., Ferns, G. A., & Avan, A. (2025) · Current Pharmaceutical Design · doi:10.2174/0113816128341167250520063502 · Cited by 8 · see citing works
Xu, R., Ma, B., Yang, Y., Dong, X., Li, J., Xu, X., & Fang, Y. (2024) · iScience · doi:10.1016/j.isci.2024.109279 · Cited by 8 · see citing works
Wang, H., Li, B., Li, A., An, C., Liu, S., & Zhuang, Z. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25116131 · Cited by 8 · see citing works
Insights on the Quest for the Structure–Function Relationship of the Mitochondrial Pyruvate Carrier
Quesñay, J. E. N., Pollock, N. L., Nagampalli, R. S. K., Lee, S. C., Balakrishnan, V., Dias, S. M. G., Moraes, I., Dafforn, T. R., & Ambrosio, A. L. B. (2020) · Biology · doi:10.3390/biology9110407 · Cited by 8 · see citing works
Mitochondrial pyruvate carrier influences ganoderic acid biosynthesis in Ganoderma lucidum
Chen, J., Xu, W., Wang, Z., Li, T., Liu, W., Ren, A., Liu, R., Zhu, J. K., & Shi, L. (2023) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-022-12357-4 · Cited by 8 · see citing works
Politte, H., Maram, L., & Elgendy, B. (2025) · Biomolecules · doi:10.3390/biom15020223 · Cited by 8 · see citing works
Pan, X., Liao, G., Li, H., Yuan, W., Xu, L., Si, H., Zhang, J., Song, J., Chen, S., Wang, Z., et al. (2025) · Pest Management Science · doi:10.1002/ps.8931 · Cited by 7 · see citing works
Peng, Y., Yan, L. E., Zhao, C., Zhang, B., Zhang, B., & Qiu, L. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26178295 · Cited by 7 · see citing works
Xing, Y., Zhang, Y., Li, J., Tang, Y., Zhang, J., Yang, R., Tang, H., Qian, H., Huang, D., Chen, W., et al. (2024) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.4c11686 · Cited by 7 · see citing works
Xu, W., Fan, J., Wang, Y., Wang, Y., Zhu, J. K., Ren, A., Yu, H., Shi, L., & Zhao, M. (2021) · FEMS Microbiology Letters · doi:10.1093/femsle/fnab088 · Cited by 7 · see citing works
Moulistanos, A., Nikolaou, T., Sismanoglou, S., Gkagkavouzis, K., Karaiskou, N., Antonopoulou, E., Triantafyllidis, A., & Papakostas, S. (2023) · Ecology and Evolution · doi:10.1002/ece3.10727 · Cited by 6 · see citing works
Wang, P., Wang, Z., Jin, X., Zhang, M., Shen, M., & Li, D. (2025) · Antioxidants · doi:10.3390/antiox14050603 · Cited by 6 · see citing works
Strong, R., Nelson, J. F., Bogue, M. A., Colca, J. R., Denzel, M. S., Diaz, V., Finck, B. N., Gladyshev, V. N., Horvath, S., Jiang, N., et al. (2025) · GeroScience · doi:10.1007/s11357-025-01881-6 · Cited by 6 · see citing works
Akhmiyati, P. A., Chen, B., Yang, Y., Liu, L., & Liu, W. (2025) · Frontiers in Veterinary Science · doi:10.3389/fvets.2025.1682137 · Cited by 6 · see citing works
Laghezza, A., Cerchia, C., Genovese, M., Montanari, R., Capelli, D., Wackerlig, J., Simić, S., Falbo, E., Pecora, L., Leuci, R., et al. (2024) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2024.116567 · Cited by 6 · see citing works
The Role of Mitochondrial Pyruvate Carrier in Neurological Disorders
Liu, Y., Yu, X., & Jiang, W. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04435-7 · Cited by 7 · see citing works
Wang, L., Liu, C., Wang, L., Xu, J., Zheng, J., Xu, Y., Jin, Z., Feng, D., Zhang, M., Yu, M., et al. (2025) · Aquaculture · doi:10.1016/j.aquaculture.2025.742172 · Cited by 6 · see citing works
Rua, A. J., Mitchell, W., Claypool, S. M., Alder, N. N., & Alexandrescu, A. T. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2024.107746 · Cited by 6 · see citing works
Kazemi, E., Zargooshi, J., Dehpahni, M. F., Motlagh, H.-R. M., Kaboudi, M., Kahrizi, D., Khazaie, H., Mahaki, B., Mohammadian, Y., & Yazdani, L. (2021) · Cellular and Molecular Biology · doi:10.14715/cmb/2021.67.2.13 · Cited by 6 · see citing works
The fate of pyruvate dictates cell growth by modulating cellular redox potentialPreprint
Toshniwal, A. G., Lam, G., Bott, A. J., Cluntun, A. A., Skabelund, R. A., Nam, H.-J., Wisidagama, D. R., Thummel, C. S., & Rutter, J. P. (2024) · eLife · doi:10.7554/elife.103705 · Cited by 6 · see citing works
Where Is the Oxygen? The Mirage of Non-Oxidative Glucose Consumption During Brain Activity
Schurr, A. (2025) · NeuroSci · doi:10.3390/neurosci6040126 · Cited by 5 · see citing works
Alberti, G., D’Amico, G., Augello, M. A., Cappello, F., Szychlinska, M. A., Bavisotto, C. C., & Scalia, F. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms27010373 · Cited by 5 · see citing works
Mitochondrial YBX1 promotes cancer cell metastasis by inhibiting pyruvate uptake
Chen, H., Ling, T., Chen, D., Liu, W., Qi, H., Xia, T., Liu, X., Wang, W., Guo, X., Otkur, W., et al. (2023) · Life Metabolism · doi:10.1093/lifemeta/load038 · Cited by 5 · see citing works
Self-citationLópez-Muguruza, E., Peiró-Moreno, C., Pérez‐Cerdá, F., Matute, C., & Ruiz, A. (2025) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2025.1557214 · Cited by 5 · see citing works
Liu, Y., Li, X.-Y., Gong, C., Cao, Y., Wang, J., Han, M., & Yang, J. (2024) · Postharvest Biology and Technology · doi:10.1016/j.postharvbio.2024.113305 · Cited by 4 · see citing works
Sperm metabolomic profiles of varicocele-associated asthenozoospermia
Hou, Y., Wang, Y., Pan, M., An, D., Zhong, M., & Zhang, Q. (2025) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2025.116908 · Cited by 4 · see citing works
Structural transport and inhibition mechanism of the mitochondrial pyruvate carrier
Lacabanne, D., Ruprecht, J. J., Sichrovsky, M., Forrest, L. R., Leone, V., Tavoulari, S., & Kunji, E. R. S. (2025) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2025.11.002 · Cited by 4 · see citing works
Glucose-derived glutamate drives neuronal terminal differentiation in vitro
D’Andrea, L., Audano, M., Pedretti, S., Pelucchi, S., Stringhi, R., Imperato, G., Cesare, G. D., Cambria, C., Laporte, M. H., Zamboni, N., et al. (2024) · EMBO Reports · doi:10.1038/s44319-023-00048-8 · Cited by 4 · see citing works
Yao, W., Sun, R., Zhang, W., Kang, J., Wu, Z., Mao, L., Yang, Y., Li, S., Song, G., Ge, J., et al. (2025) · Foods · doi:10.3390/foods14152691 · Cited by 3 · see citing works
Strategic Targeting of Mitochondria: Bridging Biology and Therapy for Health Benefits
Kurian, G. A., Jayaraman, S., & Gino, E. R. (2025) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-025-01915-y · Cited by 3 · see citing works
Chang, C.-C., Pak, J., Bae, S., Kim, G. D., & Son, H.-S. (2025) · Current Research in Food Science · doi:10.1016/j.crfs.2025.101294 · Cited by 3 · see citing works
Zhang, L., Tang, H., Zheng, J., Yu, Q., Wang, H., Li, D., Zhang, Z., & Tang, Z. (2026) · Food Research International · doi:10.1016/j.foodres.2026.118721 · Cited by 3 · see citing works
Liang, Y.-G., Wang, H.-H., Wu, Y., & Tao, Y. (2026) · Biochemical Engineering Journal · doi:10.1016/j.bej.2026.110187 · Cited by 3 · see citing works
Feyera, T., Lashkari, S., Johannsen, J. C., Llauradó-Calero, E., Li, Z., Theil, P. K., & Jensen, S. K. (2023) · Journal of Animal Science · doi:10.1093/jas/skad372 · Cited by 3 · see citing works
Molecular mechanism of circHIPK3 in mitochondrial function in septic acute kidney injury
Tang, L., Zhang, J., Han, J., Zhang, D., Zhang, H., Liu, J., & Li, X. (2024) · Environmental Toxicology · doi:10.1002/tox.24127 · Cited by 3 · see citing works
- Authors
- Zangari, J., Petrelli, F., Maillot, B., & Martinou, J.-C.
- Affiliations
- University of Geneva (CH)
- Corresponding author
- Martinou, Jean-Claude
- Venue
- Biomolecules
- Publisher
- MDPI AG
- Published
- 2020-07-17
- Volume
- 10
- Issue
- 7
- Pages
- 1068
- ISSN
- 2218-273X (ISSN-L)
- PMC
- PMC7407832
- OpenAlex
- W3042494222
- Cited by
- 172
- References
- 103
- Citations by year
- 2026: 33 · 2025: 47 · 2024: 33 · 2023: 30 · 2022: 16 · 2021: 11 · 2020: 2
- FWCI
- 1.44
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Biomolecules (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Oncosuisse (KFS-4434-02-2018)
- Swiss National Foundation (31003A_179421)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Biochemical Acid Research Studies
- Keywords
- pyruvate metabolism, mitochondrial pyruvate carrier, glycolysis, TCA cycle, oxidative phosphorylation, mitochondrial dysfunction, neurodegenerative diseases, metabolic disorders, cancer
- MeSH terms
- Animals, Gene Expression Regulation, Humans, Metabolic Diseases, Mitochondria, Neoplasms, Pyruvic Acid, Neurodegenerative Diseases, Monocarboxylic Acid Transporters, Mitochondrial Membrane Transport Proteins
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