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Oxidative stress and calcium dysregulation by palmitate in type 2 diabetes
Open accessAbstract
Free fatty acids (FFAs) are important substrates for mitochondrial oxidative metabolism and ATP synthesis but also cause serious stress to various tissues, contributing to the development of metabolic diseases. CD36 is a major mediator of cellular FFA uptake. Inside the cell, saturated FFAs are able to induce the production of cytosolic and mitochondrial reactive oxygen species (ROS), which can be prevented by co-exposure to unsaturated FFAs. There are close connections between oxidative stress and organellar Ca2+ homeostasis. Highly oxidative conditions induced by palmitate trigger aberrant endoplasmic reticulum (ER) Ca2+ release and thereby deplete ER Ca2+ stores. The resulting ER Ca2+ deficiency impairs chaperones of the protein folding machinery, leading to the accumulation of misfolded proteins. This ER stress may further aggravate oxidative stress by augmenting ER ROS production. Secondary to ER Ca2+ release, cytosolic and mitochondrial matrix Ca2+ concentrations can also be altered. In addition, plasmalemmal ion channels operated by ER Ca2+ depletion mediate persistent Ca2+ influx, further impairing cytosolic and mitochondrial Ca2+ homeostasis. Mitochondrial Ca2+ overload causes superoxide production and functional impairment, culminating in apoptosis. This vicious cycle of lipotoxicity occurs in multiple tissues, resulting in β-cell failure and insulin resistance in target tissues, and further aggravates diabetic complications. High levels of the fatty acid palmitate cause cell death and exacerbate the complications of type 2 diabetes. Kyu-Sang Park at Yonsei University Wonju College of Medicine and colleagues review the molecular mechanisms responsible for palmitate-induced toxicity. The transmembrane protein CD36 mediates the uptake of palmitate into cells where it triggers the production of reactive oxygen species (ROS). Overproduction of ROS interferes with the cell's protein-processing organelle, the endoplasmic reticulum (ER), leading to damaged misfolded proteins and to ER calcium loss. This loss further damages protein folding and increases ROS production. Moreover, it causes an influx of calcium into mitochondria, the cell's power plants, and ultimately results in cell death. Therapeutic agents that inhibit CD36, reduce ROS production or prevent ER calcium loss could break this toxic cycle and contribute to the treatment of type 2 diabetes.
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“ROS accumulation triggers damaging cascades: a decrease in mitochondrial membrane potential, activation of caspases 3/7, apoptosis, and ER stress and inflammation via NF-κB [90,152,153,154,155].”
From The HepG2 Cell Line as a Model for Studying Metabolic Dysfunction-Associated Steatotic Liver Disease (2026) · cites this paper as [153]
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Citations
Cites
Biochemistry and molecular cell biology of diabetic complications
Brownlee, M. (2001) · Nature · doi:10.1038/414813a · Cited by 9,107
Signal integration in the endoplasmic reticulum unfolded protein response
Ron, D., & Walter, P. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2199 · Cited by 6,431
Control of inositol 1,4,5-trisphosphate-induced Ca2+ release by cytosolic Ca2+
Bootman, M. D., Missiaen, L., Parys, J. B., SMEDT, H. D., & Casteels, R. (1995) · Biochemical Journal · doi:10.1042/bj3060445 · Cited by 5,131
Meijer, L., Nelson, D. J., Riazanski, V., Gabdoulkhakova, A. G., Héry-Arnaud, G., Berre, R. L., Loaëc, N., Oumata, N., Galons, H., Nowak, E., et al. (2016) · Journal of Innate Immunity · doi:10.1159/000444256 · Cited by 5,008
Mitochondrial control of cell death
Kroemer, G., & Reed, J. C. (2000) · Nature Medicine · doi:10.1038/74994 · Cited by 3,103
THE MAMMALIAN UNFOLDED PROTEIN RESPONSE
Schröder, M., & Kaufman, R. J. (2005) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.73.011303.074134 · Cited by 3,099
Fission and selective fusion govern mitochondrial segregation and elimination by autophagy
Twig, G., Elorza, A., Molina, A. J. A., Mohamed, H., Wikstrom, J. D., Walzer, G., Stiles, L., Haigh, S. E., Katz, S., Las, G., et al. (2008) · The EMBO Journal · doi:10.1038/sj.emboj.7601963 · Cited by 3,082
Triglyceride accumulation protects against fatty acid-induced lipotoxicity
Listenberger, L. L., Han, X., Lewis, S. E., Cases, S., Farese, R. V., Ory, D. S., & Schaffer, J. E. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0630588100 · Cited by 2,075
Mitochondria as sensors and regulators of calcium signalling
Rizzuto, R., De Stefani, D., Raffaello, A., & Mammucari, C. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3412 · Cited by 1,781
Redox regulation of cell survival
Trachootham, D., Lu, W., Ogasawara, M. A., Valle, N. R.-D., & Huang, P. (2008) · Antioxidants & Redox Signaling · doi:10.1089/ars.2007.1957 · Cited by 1,781
Flagged first, then by citations
Cited by
Sorted by citations
Role of Minerals and Trace Elements in Diabetes and Insulin Resistance
Dubey, P., Thakur, V., & Chattopadhyay, M. (2020) · Nutrients · doi:10.3390/nu12061864 · Cited by 407
Piao, M. J., Ahn, M. J., Kang, K. A., Ryu, Y. S., Hyun, Y. J., Shilnikova, K., Zhen, A. X., Jeong, J. W., Choi, Y. H., Kang, H. K., et al. (2018) · Archives of Toxicology · doi:10.1007/s00204-018-2197-9 · Cited by 339
“Excessive ER Ca2+ release and mitochondrial Ca2+ overload further amplify oxidative stress (Ly et al. 2017).”
The Role of Oxidative Stress in Pancreatic β Cell Dysfunction in Diabetes
Eguchi, N., Vaziri, N. D., Dafoe, D. C., & Ichii, H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041509 · Cited by 367
The aftermath of the interplay between the endoplasmic reticulum stress response and redox signaling
Bhattarai, K. R., Riaz, T. A., Kim, H., & Chae, H. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00560-8 · Cited by 356
Fatty Acid-Induced Lipotoxicity in Pancreatic Beta-Cells During Development of Type 2 Diabetes
Oh, Y. S., Bae, G. D., Baek, D. J., Park, E., & Jun, H. (2018) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00384 · Cited by 323
Changes in Plasma Free Fatty Acids Associated with Type-2 Diabetes
Sobczak, A. I. S., Blindauer, C. A., & Stewart, A. J. (2019) · Nutrients · doi:10.3390/nu11092022 · Cited by 314
Mori, Y., Ajay, A. K., Chang, J., Mou, S., Zhao, H., Kishi, S., Li, J., Brooks, C. R., Xiao, S., Woo, H., et al. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.04.004 · Cited by 304
Mechanism of increased risk of insulin resistance in aging skeletal muscle
Shou, J., Chen, P.-J., & Xiao, W.-H. (2020) · Diabetology & Metabolic Syndrome · doi:10.1186/s13098-020-0523-x · Cited by 283
Functional diversity of small nucleolar RNAs
Bratkovič, T., Božič, J., & Rogelj, B. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkz1140 · Cited by 272
Role of c-Jun N-terminal Kinase (JNK) in Obesity and Type 2 Diabetes
Yung, J. H. M., & Giacca, A. (2020) · Cells · doi:10.3390/cells9030706 · Cited by 284
Effects of Dietary n–3 and n–6 Polyunsaturated Fatty Acids in Inflammation and Cancerogenesis
Liput, K. P., Lepczyński, A., Ogłuszka, M., Nawrocka, A., Poławska, E., Grzesiak, A., Ślaska, B., Pareek, C. S., Czarnik, U., & Pierzchała, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22136965 · Cited by 271
Monounsaturated Fatty Acids in Obesity-Related Inflammation
Ravaut, G., Légiot, A., Bergeron, K., & Mounier, C. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms22010330 · Cited by 272
Targeting Oxidative Stress for the Treatment of Liver Fibrosis
Luangmonkong, T., Suriguga, S., Mutsaers, H. A. M., Groothuis, G. M. M., Olinga, P., & Boersema, M. (2018) · Reviews of physiology, biochemistry and pharmacology · doi:10.1007/112_2018_10 · Cited by 252
Recent advances in reactive oxygen species scavenging nanomaterials for wound healing
Joorabloo, A., & Liu, T. (2024) · Exploration · doi:10.1002/exp.20230066 · Cited by 237
Zhao, X., Liu, Y., Ma, R., Chen, J., Qiu, J., Du, S., Li, C., Wu, Z., Yang, X., Chen, Z., et al. (2022) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.1c24569 · Cited by 216
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
Self-citationEnvironmental Chemical Exposures and Mitochondrial Dysfunction: a Review of Recent Literature
Reddam, A., McLarnan, S. M., & Kupsco, A. J. (2022) · Current Environmental Health Reports · doi:10.1007/s40572-022-00371-7 · Cited by 192
The risk of osteoarthritis with running and aging: a 5-year longitudinal study.
Lane, N. E., Michel, B. A., Björkengren, A. G., Oehlert, J. W., Shi, H., Bloch, D. A., & Fries, J. F. (1993) · PubMed · Cited by 166
Redox changes in obesity, metabolic syndrome, and diabetes
Korać, B., Kalezic, A., Pekovic‐Vaughan, V., Korać, A., & Janković, A. (2021) · Redox Biology · doi:10.1016/j.redox.2021.101887 · Cited by 168
Vilas‐Boas, E. A., de Almeida, D. C., Roma, L. P., Ortis, F., & Carpinelli, Â. R. (2021) · Cells · doi:10.3390/cells10123328 · Cited by 163
Modulation of Cardiac Arrhythmogenesis by Epicardial Adipose Tissue
Ernault, A. C., Meijborg, V. M. F., & Coronel, R. (2021) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2021.08.037 · Cited by 139
Biotechnological production of omega-3 fatty acids: current status and future perspectives
Qin, J., Kurt, E., LBassi, T., Sa, L., & Xie, D. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1280296 · Cited by 147
Geller, S., Arribat, Y., Netzahualcoyotzi, C., Lagarrigue, S., Carneiro, L., Zhang, L., Amati, F., López‐Mejía, I. C., & Pellerin, L. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.08.004 · Cited by 117
Water Extract of Curcuma longa L. Ameliorates Non-Alcoholic Fatty Liver Disease
Mun, J., Kim, S., Yoon, H., You, Y., Kim, O., Choi, K., Lee, Y., Lee, J., Park, J., & Jun, W. (2019) · Nutrients · doi:10.3390/nu11102536 · Cited by 106
Pancreatic Beta-cell Dysfunction in Type 2 Diabetes
Khin, P. P., Lee, J. H., & Jun, H. (2023) · European Journal of Inflammation · doi:10.1177/1721727x231154152 · Cited by 127
Riaz, T. A., Junjappa, R. P., Handigund, M., Ferdous, J., Kim, H., & Chae, H. (2020) · Cells · doi:10.3390/cells9051160 · Cited by 108
Metabolic Effects of Metformin in the Failing Heart
Dziubak, A., Wójcicka, G., Wojtak, A., & Bełtowski, J. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19102869 · Cited by 99
Nemecz, M., Constantin, A. L., Dumitrescu, M., Alexandru, N., Filippi, A., Tanko, G., & Georgescu, A. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.01554 · Cited by 100
Srivastava, R., Li, Z., Russo, G., Tang, J., Bi, R., Muppirala, U. K., Chudalayandi, S., Severin, A. J., He, M., Vaitkevicius, S. I., et al. (2018) · The Plant Cell · doi:10.1105/tpc.18.00153 · Cited by 92
Bugliani, M., Mossuto, S., Grano, F., Suleiman, M., Marselli, L., Boggi, U., SIMONE, P. D., Eizirik, D. L., Cnop, M., Marchetti, P., et al. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00052 · Cited by 91
Contribution of Oxidative Stress and Impaired Biogenesis of Pancreatic β-Cells to Type 2 Diabetes
Ježek, P., Jabůrek, M., & Plecitá‐Hlavatá, L. (2018) · Antioxidants and Redox Signaling · doi:10.1089/ars.2018.7656 · Cited by 89
Subedi, A., Liu, Q., Ayyathan, D. M., Sharon, D. M., Cathelin, S., Hosseini, M., Xu, C., Voisin, V., Bader, G. D., D’Alessandro, A., et al. (2020) · Cell stem cell · doi:10.1016/j.stem.2021.06.004 · Cited by 86
Neto, M. P. C., Aquino, J. D. S., da Silva, L. D. F. R., Silva, R. D. O., Guimarães, K. S. D. L., de Oliveira, Y., de Souza, E. L., Magnani, M., Vidal, H., & Alves, J. L. D. B. (2018) · Pharmacological Research · doi:10.1016/j.phrs.2018.01.020 · Cited by 84
Gao, X., Guo, S., Zhang, S., Liu, A., Shi, L., & Zhang, Y. (2018) · Journal of Translational Medicine · doi:10.1186/s12967-018-1685-2 · Cited by 82
The Human Islet: Mini-Organ With Mega-Impact
Walker, J. T., Saunders, D. C., Briššová, M., & Powers, A. C. (2021) · Endocrine Reviews · doi:10.1210/endrev/bnab010 · Cited by 88
Veitch, S., Njock, M., Chandy, M., Siraj, M. A., Chi, L., Mak, H., Yu, K., Rathnakumar, K., Perez-Romero, C. A., Chen, Z., et al. (2022) · Cardiovascular Diabetology · doi:10.1186/s12933-022-01458-z · Cited by 82
Roy, B. (2025) · Medical Sciences · doi:10.3390/medsci13030087 · Cited by 103
Chen, Q., Su, Y., Ju, Y., Ma, K., Li, W., & Li, W. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.09.049 · Cited by 76
Deficiency of the Circadian Clock Gene Bmal1 Reduces Microglial Immunometabolism
Wang, X., Wolff, S. E. C., Korpel, N. L., Milanova, I. V., Sandu, C., Rensen, P. C. N., Kooijman, S., Cassel, J., Kalsbeek, A., Boutillier, A., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.586399 · Cited by 79
Lipid-Induced Mechanisms of Metabolic Syndrome
Denisenko, Y., Kytikovа, O. Y., Novgorodtseva, T. P., Antonyuk, M. V., Gvozdenko, T. A., & Анатольевна, К. Т. (2020) · Journal of Obesity · doi:10.1155/2020/5762395 · Cited by 81
Integrative biology of extracellular vesicles in diabetes mellitus and diabetic complications
Liu, J., Zhang, Y., Tian, Y., Huang, W. C., Tong, N., & Fu, X. (2022) · Theranostics · doi:10.7150/thno.65778 · Cited by 75
Research progress on the mechanism of beta-cell apoptosis in type 2 diabetes mellitus
You, S., Zheng, J., Chen, Y., & Huang, H. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.976465 · Cited by 71
Seufert, A. L., Hickman, J. W., Traxler, S. K., Peterson, R. M., Waugh, T. A., Lashley, S. J., Shulzhenko, N., Napier, R. J., & Napier, B. A. (2022) · eLife · doi:10.7554/elife.76744 · Cited by 72
Rinaldi, A. M., Lazareth, H., Poindessous, V., Nemazanyy, I., Sampaio, J. L., Malpetti, D., Bignon, Y., Naesens, M., Rabant, M., Anglicheau, D., et al. (2022) · JCI Insight · doi:10.1172/jci.insight.161783 · Cited by 72
Liu, M., Mu, J., Wang, M., Hu, C., Ji, J., Wen, C., & Zhang, D. (2023) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2023.131918 · Cited by 66
Sources and triggers of oxidative damage in neurodegeneration
Angelova, P. R. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.07.003 · Cited by 67
From obesity to Alzheimer's disease through insulin resistance
Terzo, S., Amato, A., & Mulè, F. (2021) · Journal of Diabetes and its Complications · doi:10.1016/j.jdiacomp.2021.108026 · Cited by 63
Li, X., Li, Z., Dong, X., Wu, Y., Li, B., Kuang, B., Chen, G., & Zhang, L. (2023) · Phytotherapy Research · doi:10.1002/ptr.7798 · Cited by 65
Martínez‐Klimova, E., Aparicio‐Trejo, O. E., Gómez‐Sierra, T., Jiménez‐Uribe, A. P., Bellido, B., & Pedraza‐Chaverrí, J. (2020) · BioFactors · doi:10.1002/biof.1673 · Cited by 62
Remodeling of Mitochondrial Plasticity: The Key Switch from NAFLD/NASH to HCC
Longo, M., Paolini, E., Meroni, M., & Dongiovanni, P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22084173 · Cited by 61
A Brief Review of the Mechanisms of β-Cell Dedifferentiation in Type 2 Diabetes
Khin, P. P., Lee, J., & Jun, H. (2021) · Nutrients · doi:10.3390/nu13051593 · Cited by 62
Kim, C., & Choi, K. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.119607 · Cited by 65
Ophiopogonin D alleviates diabetic myocardial injuries by regulating mitochondrial dynamics
Li, W., Ji, L., Tian, J., Tang, W., Shan, X., Zhao, P., Chen, H., Zhang, C., Xu, M. G., Lü, R., et al. (2021) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2021.113853 · Cited by 60
Lin, K.-J., Wang, T., Chen, S., Lin, K.-L., Liou, C., Lan, M., Chuang, Y., Chuang, J., Wang, P., Lee, J., et al. (2021) · Antioxidants · doi:10.3390/antiox10121935 · Cited by 63
Protein aggregation: Consequences, mechanism, characterization and inhibitory strategies
Majid, N., & Khan, R. H. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.125123 · Cited by 59
Molecular mechanisms of lipotoxicity-induced pancreatic β-cell dysfunction
Benito‐Vicente, A., Jebari‐Benslaiman, S., Galicia-García, U., Larrea, A., Uribe, K. B., & Martín, C. (2021) · International review of cytology · doi:10.1016/bs.ircmb.2021.02.013 · Cited by 59
Metabolites of Gut Microbiota and Possible Implication in Development of Diabetes Mellitus
Guo, Z., Pan, J., Zhu, H., & Chen, Z. (2022) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.1c07851 · Cited by 58
The Effect of Omega-3 Fatty Acids on Insulin Resistance
Sinha, S., Haque, M., Lugova, H., & Kumar, S. (2023) · Life · doi:10.3390/life13061322 · Cited by 59
Shaping of Innate Immune Response by Fatty Acid Metabolite Palmitate
Tzeng, H., Chyuan, I., & Chen, W. (2019) · Cells · doi:10.3390/cells8121633 · Cited by 59
Karamzad, N., Maleki, V., Carson‐Chahhoud, K., Azizi, S., Sahebkar, A., & Gargari, B. P. (2019) · BioFactors · doi:10.1002/biof.1569 · Cited by 55
Seeley, E. H., Liu, Z., Yuan, S. S., Stroope, C., Cockerham, E. D., Rashdan, N. A., Delgadillo, L. F., Finney, A. C., Kumar, D., Das, S. R., et al. (2023) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.122.318684 · Cited by 52
Wang, S., Xu, L., Lu, Y., Liu, Y.-F., Han, B., Liu, T., Tang, J., Li, J. X., Wu, J., Li, J., et al. (2017) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2017.02.048 · Cited by 51
Lipotoxic Impairment of Mitochondrial Function in β-Cells: A Review
Römer, A., Linn, T., & Petry, S. F. (2021) · Antioxidants · doi:10.3390/antiox10020293 · Cited by 52
CD47 and thrombospondin-1 regulation of mitochondria, metabolism, and diabetes
Roberts, D. D., & Isenberg, J. S. (2021) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00175.2021 · Cited by 50
Cai, T., Wu, H., Qin, J., Qiao, J., Yang, Y., Wu, Y. M., Qiao, D., Xu, H. X., & Cao, Y. (2019) · LWT · doi:10.1016/j.lwt.2019.108455 · Cited by 47
High Dietary Fat Consumption Impairs Axonal Mitochondrial Function In Vivo
Sajic, M., Rumora, A. E., Kanhai, A. A., Dentoni, G., Varatharajah, S., Casey, C. S., Brown, R. D. R., Peters, F., Hinder, L. M., Savelieff, M. G., et al. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1852-20.2021 · Cited by 47
Oh, B. (2023) · Experimental & Molecular Medicine · doi:10.1038/s12276-023-01067-0 · Cited by 51
Maghsoudi, A. S., Hassani, S., Momtaz, S., Shadboorestan, A., Ganjali, M. R., Ghahremani, M. H., Hosseini, R., Norouzi, P., & Abdollahi, M. R. (2018) · Toxicology · doi:10.1016/j.tox.2018.10.014 · Cited by 45
Su, Y., Chen, Q., Ma, K., Ju, Y., Ji, T., Wang, Z., Li, W., & Li, W. (2018) · Pharmacological Reports · doi:10.1016/j.pharep.2018.12.008 · Cited by 45
Nascè, A., Gariani, K., Jornayvaz, F. R., & Szántó, I. (2022) · Antioxidants · doi:10.3390/antiox11061131 · Cited by 49
Type 2 Diabetes and Alzheimer’s Disease: The Emerging Role of Cellular Lipotoxicity
Marrano, N., Biondi, G., Borrelli, A., Rella, M., Zambetta, T., Gioia, L. D., Caporusso, M., Logroscino, G., Perrini, S., Giorgino, F., et al. (2023) · Biomolecules · doi:10.3390/biom13010183 · Cited by 44
Xia, J., Yu, J., Xu, H., Zhou, Y., Li, H., Yin, S., Xu, D., Wang, Y., Xia, H., Liao, W., et al. (2023) · Pharmacological Research · doi:10.1016/j.phrs.2023.106647 · Cited by 44
Ma, B., Ju, A., Zhang, S., An, Q., Xu, S., Liu, J., Yu, L., Fu, Y., & Luo, Y. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01437-0 · Cited by 43
Self-citationLiu, X., Zeng, X., Chen, X., Luo, R., Li, L., Wang, C., Liu, J., Cheng, J., Lu, Y., & Chen, Y. (2019) · Endocrine · doi:10.1007/s12020-019-01867-3 · Cited by 43
Han, Y., Su, Y., Han, M., Liu, Y., Shi, Q., Li, X., Wang, P., Li, W., & Li, W. (2022) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2022.115923 · Cited by 42
Wang, X., Chen, S., He, J., Chen, W., Ding, Y., Huang, J., & Huang, J. (2020) · Metabolism · doi:10.1016/j.metabol.2020.154404 · Cited by 42
Ye, M., Qiu, H., Cao, Y., Zhang, M., Mi, Y., Yu, J., & Wang, C. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00148 · Cited by 41
RetractedRole of mitochondria in pathogenesis of type 2 diabetes mellitus
Prasun, P. (2020) · Journal of Diabetes & Metabolic Disorders · doi:10.1007/s40200-020-00679-x · Cited by 45
Increased glycolysis is an early consequence of palmitate lipotoxicity mediated by redox signaling
Kakimoto, P. A., Serna, J. D. C., Ramos, V. D. M., Antonio Zorzano, A., & Kowaltowski, A. J. (2021) · Redox Biology · doi:10.1016/j.redox.2021.102026 · Cited by 41
Anwer, M. D. A., & Wei, M. Q. (2024) · Food Science and Biotechnology · doi:10.1007/s10068-024-01630-z · Cited by 46
Taddeo, E. P., Alsabeeh, N., Baghdasarian, S., Wikström, J. D., Ritou, E., Sereda, S. B., Erion, K., Li, J., Stiles, L., Abdulla, M., et al. (2019) · Diabetes · doi:10.2337/db19-0379 · Cited by 40
Differential effects of saturated and unsaturated free fatty acids on ferroptosis in rat β-cells
Krümmel, B., von Hanstein, A., Plötz, T., Lenzen, S., & Mehmeti, I. (2022) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2022.109013 · Cited by 40
Oberhauser, L., & Maechler, P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms23010324 · Cited by 41
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Miao, Z., Miao, Z., Feng, S., & Xu, S. (2023) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2023.109053 · Cited by 38
Self-citationAyeleso, T. B., Ramachela, K., & Mukwevho, E. (2018) · Molecules · doi:10.3390/molecules23082058 · Cited by 39
Kim, S. H., Kim, C., & Park, S. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18091947 · Cited by 37
Sindhu, S. T. A. K., Akhter, N., Wilson, A., Thomas, R., Arefanian, H., Madhoun, A. S. A., Al‐Mulla, F., & Ahmad, R. (2020) · Cells · doi:10.3390/cells9081799 · Cited by 38
Adzigbli, L., Sokolov, E. P., Ponsuksili, S., & Sokolova, I. M. (2021) · Journal of Experimental Biology · doi:10.1242/jeb.243304 · Cited by 37
John, A. S. P., Kundu, S., Pushpakumar, S. B., Amin, M., Tyagi, S. C., & Sen, U. (2019) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00251.2018 · Cited by 37
Ravi, S., & Gunawan, R. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009589 · Cited by 35
Cremonini, E., & Oteiza, P. I. (2018) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2018.03.027 · Cited by 36
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Keenan, S. N., Watt, M. J., & Montgomery, M. K. (2020) · Current Diabetes Reports · doi:10.1007/s11892-020-01300-4 · Cited by 38
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Roham, P. H., Save, S. N., & Sharma, S. (2022) · Journal of Pharmaceutical Analysis · doi:10.1016/j.jpha.2022.04.001 · Cited by 37
Nguyen, H. T., Polo, C. N., Wiederkehr, A., Wollheim, C. B., & Park, K. (2023) · British Journal of Pharmacology · doi:10.1111/bph.16160 · Cited by 35
Self-citationSerbis, A., Giapros, V. I., Tsamis, K. I., Balomenou, F., Galli‐Τsinopoulou, A., & Siomou, E. C. (2023) · Nutrients · doi:10.3390/nu15092217 · Cited by 42
Pan, M., Han, Y., Basu, A., Dai, A., Si, R., Willson, C., Balistrieri, A., Scott, B. T., & Makino, A. (2018) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00350.2017 · Cited by 34
Bourebaba, L., Łyczko, J., Alicka, M., Bourebaba, N., Szumny, A., Fal, A., & Marycz, K. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9051294 · Cited by 34
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Vilas‐Boas, E. A., Nalbach, L., Ampofo, E., Lucena, C. F., Naudet, L., Ortis, F., Carpinelli, Â. R., Morgan, B., & Roma, L. P. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.11.023 · Cited by 33
Metadata
- Authors
- Ly, L. D., Xu, S., Choi, S.-K., Ha, C.-M., Thoudam, T., Cha, S.-K., Wiederkehr, A., Wollheim, C. B., Lee, I.-K., & Park, K.-S.
- Affiliations
- Yonsei University (KR)
- Kyungpook National University Hospital (KR)
- University of Geneva (CH)
- Corresponding author
- Park, Kyu-Sang
- ORCID
- Venue
- Experimental & Molecular Medicine
- Published
- 2017-02-03
- Volume
- 49
- Issue
- 2
- Pages
- e291-e291
- ISSN
- 1226-3613 (ISSN-L)
- 2092-6413
- PMC
- PMC5336562
- OpenAlex
- W2584561009
- Cited by
- 378
- References
- 161
- Citations by year
- 2026: 30 · 2025: 44 · 2024: 36 · 2023: 53 · 2022: 42 · 2021: 60 · 2020: 39 · 2019: 35 · 2018: 32 · 2017: 5
- FWCI
- 3.57
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Experimental & Molecular Medicine (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Archive ouverte UNIGE (University of Geneva) (publishedVersion, other-oa)
- Archive ouverte UNIGE (University of Geneva) (submittedVersion, cc-by)
- Funders
- Korea Health Industry Development Institute (HI16C1501)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Endoplasmic Reticulum Stress and Disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Neuroscience › Sensory Systems › Ion Channels and Receptors
- Keywords
- palmitate, lipotoxicity, type 2 diabetes, oxidative stress, calcium homeostasis, CD36, free fatty acids, reactive oxygen species, endoplasmic reticulum calcium depletion, endoplasmic reticulum stress, protein misfolding, mitochondrial calcium overload, apoptosis, beta-cell failure, insulin resistance, unsaturated fatty acids
- MeSH terms
- Animals, Calcium, Diabetes Mellitus, Type 2, Endoplasmic Reticulum, Fatty Acids, Nonesterified, Humans, Mitochondria, Palmitic Acids, Reactive Oxygen Species, Oxidative Stress, CD36 Antigens, Insulin-Secreting Cells, Endoplasmic Reticulum Stress
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