Activating transcription factor 3, glucolipid metabolism, and metabolic diseases
Open accessAbstract
Lipids and glucose exert many essential physiological functions, such as providing raw materials or energy for cellular biosynthesis, regulating cell signal transduction, and maintaining a constant body temperature. Dysregulation of lipid and glucose metabolism can lead to glucolipid metabolic disorders linked to various metabolic diseases, such as obesity, diabetes, and cardiovascular disease. Therefore, intervention in glucolipid metabolism is a key therapeutic strategy for the treatment of metabolic diseases. Activating transcription factor 3 (ATF3) is a transcription factor that acts as a hub of the cellular adaptive-response network and plays a pivotal role in the regulation of inflammation, apoptosis, DNA repair, and oncogenesis. Emerging evidence has illustrated the vital roles of ATF3 in glucolipid metabolism. ATF3 inhibits intestinal lipid absorption, enhances hepatic triglyceride hydrolysis and fatty acid oxidation, promotes macrophage reverse cholesterol transport, and attenuates the progression of western diet-induced nonalcoholic fatty liver disease and atherosclerosis. In addition to its role in lipid metabolism, ATF3 has also been identified as an important regulator of glucose metabolism. Here, we summarize the recent advances in the understanding of ATF3, mainly focusing on its role in glucose and lipid metabolism and potential therapeutic implications.
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ATF3 is an important regulator of glucose and lipid metabolism in various tissues.
“The literature data suggest that ATF3 also is an important regulator of glucose and lipid metabolism in various tissues [43].”
From 20-Hydroxyecdysone Boosts Energy Production and Biosynthetic Processes in Non-Transformed Mouse Cells (2024) · cites this paper as [43]
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Cites
Progress and challenges in translating the biology of atherosclerosis
Libby, P., Ridker, P. M., & Hansson, G. K. (2011) · Nature · doi:10.1038/nature10146 · Cited by 4,010 · see citing works
Adiponectin and adiponectin receptors in insulin resistance, diabetes, and the metabolic syndrome
Kadowaki, T. (2006) · Journal of Clinical Investigation · doi:10.1172/jci29126 · Cited by 2,824 · see citing works
Macrophages in the Pathogenesis of Atherosclerosis
Moore, K. J., & Tabas, I. (2011) · Cell · doi:10.1016/j.cell.2011.04.005 · Cited by 2,669 · see citing works
Adipogenesis and metabolic health
Ghaben, A. L., & Scherer, P. E. (2019) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-018-0093-z · Cited by 1,395 · see citing works
Binding of a nuclear protein to the cyclic-AMP response element of the somatostatin gene
Montminy, M., & Bilezikjian, L. M. (1987) · Nature · doi:10.1038/328175a0 · Cited by 1,390 · see citing works
Chávez-Talavera, O., Tailleux, A., Lefebvre, P., & Staels, B. (2017) · Gastroenterology · doi:10.1053/j.gastro.2017.01.055 · Cited by 970 · see citing works
Altered adipose tissue and adipocyte function in the pathogenesis of metabolic syndrome
Kahn, C. R., Wang, G., & Lee, K. Y. (2019) · Journal of Clinical Investigation · doi:10.1172/jci129187 · Cited by 656 · see citing works
Adipokine dysregulation and adipose tissue inflammation in human obesity
Unamuno, X., Gómez‐Ambrosi, J., Rodríguez, A., Becerril, S., Frühbeck, G., & Catalán, V. (2018) · European Journal of Clinical Investigation · doi:10.1111/eci.12997 · Cited by 610 · see citing works
Nardo, D. D., Labzin, L. I., Kono, H., Seki, R., Schmidt, S. V., Beyer, M., Xu, D., Zimmer, S., Lahrmann, C., Schildberg, F. A., et al. (2013) · Nature Immunology · doi:10.1038/ni.2784 · Cited by 463 · see citing works
Guo, L., Li, X., & Tang, Q.-Q. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.r114.619957 · Cited by 354 · see citing works
Coronary Artery Disease: From Mechanism to Clinical Practice
Shao, C., Wang, J., Tian, J., & Tang, Y. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-2517-9_1 · Cited by 345 · see citing works
Master Regulator Activating Transcription Factor 3 (ATF3) in Metabolic Homeostasis and Cancer
Ku, H.-C., & Cheng, C.-F. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.00556 · Cited by 345 · see citing works
Role for Activating Transcription Factor 3 in Stress-Induced β-Cell Apoptosis
Hartman, M. G., Lü, D., Kim, M.-L., Kociba, G. J., Shukri, T., Buteau, J., Wang, X., Frankel, W. L., D, D. C. G., Prentki, M., et al. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.13.5721-5732.2004 · Cited by 313 · see citing works
Regulation of glucose and lipid metabolism in health and disease
Chen, L., Chen, X., Huang, X., Song, B., Wang, Y., & Wang, Y. (2019) · Science China Life Sciences · doi:10.1007/s11427-019-1563-3 · Cited by 309 · see citing works
Inter-organ cross-talk in metabolic syndrome
Priest, C., & Tontonoz, P. (2019) · Nature Metabolism · doi:10.1038/s42255-019-0145-5 · Cited by 279 · see citing works
Pro-resolving lipid mediators: regulators of inflammation, metabolism and kidney function
Brennan, E. P., Kantharidis, P., Cooper, M. E., & Godson, C. (2021) · Nature Reviews Nephrology · doi:10.1038/s41581-021-00454-y · Cited by 274 · see citing works
Transcriptional and Epigenomic Regulation of Adipogenesis
Lee, J., Schmidt, H., Lai, B., & Ge, K. (2019) · Molecular and Cellular Biology · doi:10.1128/mcb.00601-18 · Cited by 265 · see citing works
Structural determinants for transcriptional activation by cAMP-responsive DNA elements.
Deutsch, P., Hoeffler, J. P., Jameson, J. L., Lin, J. C., & Habener, J. F. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)81381-9 · Cited by 257 · see citing works
Chen, B. P. C., Liang, G., Whelan, J., & Hai, T. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)40754-x · Cited by 249 · see citing works
Intestinal absorption of bile acids in health and disease
Ticho, A. L., Malhotra, P., Dudeja, P. K., Gill, R. K., & Alrefai, W. A. (2019) · Comprehensive physiology · doi:10.1002/cphy.c190007 · Cited by 215 · see citing works
Negative Regulation of TLR-Signaling Pathways by Activating Transcription Factor-3
Whitmore, M., Iparraguirre, A., Kubelka, L., Weninger, W., Hai, T., & Williams, B. R. G. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.6.3622 · Cited by 214 · see citing works
Nrf2 and oxidative stress in liver ischemia/reperfusion injury
Bardallo, R. G., Rosello, A. P., Sánchez-Nuño, S., Alva, N., Roselló‐Catafau, J., & Carbonell, T. (2021) · FEBS Journal · doi:10.1111/febs.16336 · Cited by 208 · see citing works
Hoetzenecker, W., Echtenacher, B., Guenova, E., Hoetzenecker, K., Woelbing, F., Brück, J., Teske, A., Valtcheva, N., Fuchs, K., Kneilling, M., et al. (2011) · Nature Medicine · doi:10.1038/nm.2557 · Cited by 192 · see citing works
Inter‐organ communication: a gatekeeper for metabolic health
Castillo‐Armengol, J., Fajas, L., & Lopez‐Mejia, I. C. (2019) · The EMBO Reports · doi:10.15252/embr.201947903 · Cited by 178 · see citing works
Gold, E. S., Ramsey, S. A., Sartain, M. J., Selinummi, J., Podolsky, I., Rodriguez, D. J., Moritz, R. L., & Aderem, A. A. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20111202 · Cited by 154 · see citing works
Kawauchi, J., Zhang, C., Nobori, K., Hashimoto, Y., Adachi, M. T., Noda, A., Sunamori, M., & Kitajima, S. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m202974200 · Cited by 131 · see citing works
The Roles of ATF3 in Glucose Homeostasis
Allen-Jennings, A. E., Hartman, M. G., Kociba, G. J., & Hai, T. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m100986200 · Cited by 116 · see citing works
Zhao, J. C., Li, X., Guo, M., Yu, J., & Yan, C. (2016) · BMC Genomics · doi:10.1186/s12864-016-2664-8 · Cited by 114 · see citing works
NFATc4 and ATF3 Negatively Regulate Adiponectin Gene Expression in 3T3-L1 Adipocytes
Kim, H. B., Kong, M., Kim, T., et al. (2006) · Diabetes · doi:10.2337/db05-1507 · Cited by 108 · see citing works
Kwon, J.-W., Kwon, H., Shin, H., Choi, Y.-M., Anwar, M. A., & Choi, S. (2015) · Scientific Reports · doi:10.1038/srep14470 · Cited by 100 · see citing works
The Drosophila MAPK p38c Regulates Oxidative Stress and Lipid Homeostasis in the Intestine
Chakrabarti, S., Poidevin, M., & Lemaître, B. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004659 · Cited by 96 · see citing works
Kim, J. Y., Song, E. H., Lee, H. J., Oh, Y. K., Park, Y. S., Park, J.-W., Kim, B. J., Kim, D. J., Lee, I., Song, J., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.142315 · Cited by 94 · see citing works
Hepatocyte ATF3 protects against atherosclerosis by regulating HDL and bile acid metabolism
Xu, Y., Li, Y., Jadhav, K. S., Pan, X., Zhu, Y., Hu, S., Chen, S., Chen, L., Tang, Y., Wang, H. H., et al. (2021) · Nature Metabolism · doi:10.1038/s42255-020-00331-1 · Cited by 91 · see citing works
Self-citationZmuda, E. J., Qi, L., Zhu, M. X., Mirmira, R. G., Montminy, M., & Hai, T. (2010) · Molecular Endocrinology · doi:10.1210/me.2009-0463 · Cited by 90 · see citing works
Activating Transcription Factor 3 Regulates Immune and Metabolic Homeostasis
Ryneš, J., Donohoe, C. D., Frommolt, P., Brodesser, S., Jindra, M., & Uhlířová, M. (2012) · Molecular and Cellular Biology · doi:10.1128/mcb.00429-12 · Cited by 80 · see citing works
Clément, M., Basatemur, G., Masters, L. M., Baker, L. L., Bruneval, P., Iwawaki, T., Kneilling, M., Yamasaki, S., GOODALL, J. C., & Mallat, Z. (2016) · Circulation · doi:10.1161/circulationaha.116.022668 · Cited by 79 · see citing works
Kim, W., Park, K. J., Hwang, J., Kim, G. H., Lee, D.-Y., Lee, Y. J., Song, E. H., Yoo, M., Kim, B.-J., Suh, Y. H., et al. (2017) · Journal of Hepatology · doi:10.1016/j.jhep.2017.03.023 · Cited by 79 · see citing works
Adipocyte dedifferentiation in health and diseases
Song, T., & Kuang, S. (2019) · Clinical Science · doi:10.1042/cs20190128 · Cited by 79 · see citing works
Nawa, T., Nawa, M., Adachi, M. T., UCHIMURA, I., Shimokawa, R., Fujisawa, K., Tanaka, A., Numano, F., & Kitajima, S. (2002) · Atherosclerosis · doi:10.1016/s0021-9150(01)00639-6 · Cited by 78 · see citing works
Transcriptional factor ATF3 promotes liver fibrosis via activating hepatic stellate cells
Shi, Z., Zhang, K., Chen, T., Zhang, Y., Du, X., Zhao, Y., Shao, S., Zheng, L., Han, T., & Wei, H. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-03271-6 · Cited by 75 · see citing works
Self-citationActivating transcription factor 3 in immune response and metabolic regulation
Jadhav, K. S., & Zhang, Y. (2017) · Liver Research · doi:10.1016/j.livres.2017.08.001 · Cited by 72 · see citing works
Self-citationAdipocyte browning and resistance to obesity in mice is induced by expression of ATF3
Cheng, C., Ku, H., Cheng, J., Chao, S.-W., Li, H., Lai, P., Chang, C., Don, M., Chen, H.-H., & Lin, H. (2019) · Communications Biology · doi:10.1038/s42003-019-0624-y · Cited by 71 · see citing works
Zhu, Q., Wang, H., Jiang, B., Ni, X., Jiang, L., Li, C., Wang, X., Zhang, F., Ke, B., & Lü, L. (2018) · Cell Death and Disease · doi:10.1038/s41419-018-0894-1 · Cited by 65 · see citing works
ATF3 inhibits adipocyte differentiation of 3T3-L1 cells
Jang, M. K., Kim, C. H., Seong, J. K., & Jung, M. H. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.03.104 · Cited by 57 · see citing works
Zmuda, E. J., Viapiano, M. S., Grey, S. T., Hadley, G. A., Garcı́a-Ocaña, A., & Hai, T. (2010) · Diabetologia · doi:10.1007/s00125-010-1696-x · Cited by 57 · see citing works
Genomic Characterization of Metformin Hepatic Response
Luizon, M. R., Eckalbar, W. L., Wang, Y., Jones, S. L., Smith, R. P., Megan, L., Lin, L., Gallins, P. J., Etheridge, A. S., Wright, F. A., et al. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006449 · Cited by 49 · see citing works
ATF3 acts as a rheostat to control JNK signalling during intestinal regeneration
Zhou, J., Edgar, B. A., & Boutros, M. (2017) · Nature Communications · doi:10.1038/ncomms14289 · Cited by 49 · see citing works
Dai, Z., Wang, X., Peng, R., Zhang, B., Han, Q., Lin, J., Wang, J., Lin, J., Jiang, M., Liu, H., et al. (2021) · Cancer Letters · doi:10.1016/j.canlet.2021.10.024 · Cited by 49 · see citing works
Hypothalamic ATF3 is involved in regulating glucose and energy metabolism in mice
Lee, Y., Sasaki, T., Kobayashi, M., Kikuchi, O., Kim, H.-J., Yokota‐Hashimoto, H., Shimpuku, M., Susanti, V. Y., Ido-Kitamura, Y., Kimura, K., et al. (2013) · Diabetologia · doi:10.1007/s00125-013-2879-z · Cited by 45 · see citing works
AdipoR2 is transcriptionally regulated by ER stress‐inducible ATF3 in HepG2 human hepatocyte cells
Koh, I.-U., Lim, J. H., Joe, M. K., Kim, W., Jung, M. H., Yoon, J. B., & Song, J. (2010) · FEBS Journal · doi:10.1111/j.1742-4658.2010.07646.x · Cited by 42 · see citing works
Xu, Y., Hu, S., Jadhav, K. S., Zhu, Y., Pan, X., Bawa, F. N. C., Yin, L., & Zhang, Y. (2021) · Diabetes · doi:10.2337/db21-0181 · Cited by 42 · see citing works
Self-citationThe New Therapeutic Approaches in the Treatment of Non-Alcoholic Fatty Liver Disease
Filipović, B. F., Lukić, S., Mijac, D. D., Marjanovic-Haljilji, M., Vojnović, M., Bogdanović, J. M., Glišić, T., Filipović, N., Kiswani, J. A., Djoković, A., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222413219 · Cited by 42 · see citing works
Fang, J., Ji, Y., Zhang, P., Cheng, L., Chen, Y., Chen, J., Su, Y., Cheng, X., Zhang, Y., Li, T., et al. (2019) · Hepatology · doi:10.1002/hep.30950 · Cited by 39 · see citing works
Self-citationWang, Y., Gao, H., Wang, F., Ye, Z., Mokrý, M., Turner, A. W., Ye, J., Koplev, S., Luo, L., Alsaigh, T., et al. (2021) · Cardiovascular Research · doi:10.1093/cvr/cvab347 · Cited by 39 · see citing works
Tu, C., Xiong, H. Y., Hu, Y., Wang, W., Mei, G., Wang, H., Li, Y., Zhou, Z., Meng, F., Zhang, P., et al. (2020) · Hepatology · doi:10.1002/hep.31202 · Cited by 37 · see citing works
Jeong, B. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.03.214 · Cited by 35 · see citing works
Adipose tissue development and the molecular regulation of lipid metabolism
Raajendiran, A., Tsiloulis, T., & Watt, M. J. (2016) · Essays in Biochemistry · doi:10.1042/ebc20160042 · Cited by 32 · see citing works
Qian, L., Zhao, Y., Guo, L., et al. (2017) · Journal of Cellular Physiology · doi:10.1002/jcp.25849 · Cited by 32 · see citing works
ATF3 represses PPARγ expression and inhibits adipocyte differentiation
Jang, M.-K., & Jung, M. H. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.10.028 · Cited by 30 · see citing works
Wang, A., Arantes, S., Conti, C. J., McArthur, M. J., Aldaz, C. M., & MacLeod, M. C. (2007) · Molecular Carcinogenesis · doi:10.1002/mc.20298 · Cited by 30 · see citing works
Favre, D., Gouill, E. L., Fahmi, D., Verdumo, C., Chinetti, G., Staels, B., Caiazzo, R. J., Pattou, F. N., Lê, K., Tappy, L., et al. (2011) · Diabetes · doi:10.2337/db10-1743 · Cited by 30 · see citing works
Ku, H., Chan, T.-Y., Chung, J.-F., Kao, Y., & Cheng, C. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.112440 · Cited by 29 · see citing works
Kim, S. Y., Hwang, S., Lee, B., Hong, J. A., Sung, Y. H., & Kim, I. (2022) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2022.109806 · Cited by 25 · see citing works
Lee, Y. M., Uhm, K.-O., Lee, E. S., et al. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.04.003 · Cited by 24 · see citing works
He, F., Zhou, M., Yu, T., et al. (2016) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjw021 · Cited by 22 · see citing works
Sulfuretin Prevents Obesity and Metabolic Diseases in Diet Induced Obese Mice
Kim, S., Song, N., Chang, S., Bahn, G., Choi, Y., Rhee, D. K., Yun, U. J., Choi, J., Lee, J., Yoo, J. H., et al. (2018) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2018.090 · Cited by 22 · see citing works
Overexpression of activating transcription factor 3 exerts suppressive effects in HepG2 cells
Li, X., Zang, S., Cheng, H., et al. (2018) · Molecular Medicine Reports · doi:10.3892/mmr.2018.9707 · Cited by 20 · see citing works
Wu, S., Hsu, L., Cheng, C., et al. (2011) · Clinica Chimica Acta · doi:10.1016/j.cca.2011.02.011 · Cited by 19 · see citing works
Fernández‐Verdejo, R., Vanwynsberghe, A. M., Hai, T., et al. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.08.059 · Cited by 15 · see citing works
Role of activating transcription factor 3 in fructose-induced metabolic syndrome in mice
Chou, C., Li, C.-H., Lin, H., et al. (2018) · Hypertension Research · doi:10.1038/s41440-018-0058-9 · Cited by 14 · see citing works
The Role of Mondo Family Transcription Factors in Nutrient-Sensing and Obesity
Ke, H., Luan, Y., Wu, S., Zhu, Y., & Tong, X. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.653972 · Cited by 14 · see citing works
Lee, Y., Kobayashi, M., Kikuchi, O., et al. (2013) · Endocrine Journal · doi:10.1507/endocrj.ej13-0383 · Cited by 13 · see citing works
Nagahara, R., Matono, T., Sugihara, T., Matsuki, Y., Yamane, M., Okamoto, T., Miyoshi, K., Nagahara, T., Okano, J., Koda, M., et al. (2019) · Yonago acta medica · doi:10.33160/yam.2019.03.006 · Cited by 12 · see citing works
Regulation of toll-like receptors expression in muscle cells by exercise-induced stress
Park, J.-W., Kim, K.-H., Choi, J.-K., Park, T. S., Song, K., & Cho, B.-W. (2020) · Animal Bioscience · doi:10.5713/ab.20.0484 · Cited by 9 · see citing works
LINC00238 inhibits hepatic carcinoma progression by activating TMEM106C‑mediated apoptosis pathway
Jiang, C., Li, F., Yang, M., Duan, J., Lai, J., Sun, S., & Fan, S. (2021) · Molecular Medicine Reports · doi:10.3892/mmr.2021.12397 · Cited by 8 · see citing works
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- Authors
- Hu, S., Zhao, X., Li, R., Hu, C., Wu, H., Li, J., Zhang, Y., & Xu, Y.
- Affiliations
- Northeast Ohio Medical University (US)
- Shanghai Medical College of Fudan University (CN)
- Capital Medical University (CN)
- Corresponding author
- Hu, Shuwei
- Zhang, Yanqiao
- Xu, Yanyong
- Venue
- Journal of Molecular Cell Biology
- Publisher
- Oxford University Press (OUP)
- Published
- 2022-10
- Volume
- 14
- Issue
- 10
- ISSN
- 1674-2788 (ISSN-L)
- 1759-4685
- PMC
- PMC10076183
- OpenAlex
- W4310780158
- Cited by
- 33
- References
- 75
- Citations by year
- 2026: 9 · 2025: 11 · 2024: 10 · 2023: 3
- FWCI
- 1.96
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Journal of Molecular Cell Biology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- National Natural Science Foundation of China (32271218, 81670519)
- Science and Technology Commission of Shanghai Municipality (22ZR1414300)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Lipid metabolism and biosynthesis
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipid metabolism and disorders
- Keywords
- ATF3, glucolipid metabolism, glucose metabolism, lipid metabolism, metabolic disorders, obesity, diabetes mellitus, cardiovascular disease, intestinal lipid absorption, fatty acid oxidation, reverse cholesterol transport, macrophages, non-alcoholic fatty liver disease, atherosclerosis, Western diet, transcriptional regulation
- MeSH terms
- Glucose, Humans, Lipids, Liver, Metabolic Diseases, Lipid Metabolism, Activating Transcription Factor 3
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