ER Stress Drives Lipogenesis and Steatohepatitis via Caspase-2 Activation of S1P
Open accessAbstract
Nonalcoholic fatty liver disease (NAFLD) progresses to nonalcoholic steatohepatitis (NASH) in response to elevated endoplasmic reticulum (ER) stress. Whereas the onset of simple steatosis requires elevated de novo lipogenesis, progression to NASH is triggered by accumulation of hepatocyte-free cholesterol. We now show that caspase-2, whose expression is ER-stress inducible and elevated in human and mouse NASH, controls the buildup of hepatic-free cholesterol and triglycerides by activating sterol regulatory element-binding proteins (SREBP) in a manner refractory to feedback inhibition. Caspase-2 colocalizes with site 1 protease (S1P) and cleaves it to generate a soluble active fragment that initiates SCAP-independent SREBP1/2 activation in the ER. Caspase-2 ablation or pharmacological inhibition prevents diet-induced steatosis and NASH progression in ER-stress-prone mice. Caspase-2 inhibition offers a specific and effective strategy for preventing or treating stress-driven fatty liver diseases, whereas caspase-2-generated S1P proteolytic fragments, which enter the secretory pathway, are potential NASH biomarkers.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
ER stress might contribute to the development of increased hepatic DNL in hepatic IR, at least in advanced stages of MASLD/MASH.
“Thus, ER stress might contribute to the development of increased hepatic DNL in hepatic IR, at least in the advanced stages of MASLD/MASH [91].”
From Hepatic Insulin Resistance and Steatosis in Metabolic Dysfunction-Associated Steatotic Liver Disease: New Insights into Mechanisms and Clinical Implications (2025) · cites this paper as [91]
ER-stress-mediated SREBP1/2 activation, TG and cholesterol accumulation, as well as MASH progression, all depend on Casp2.
“A study showed that ER-stress-mediated SREBP1/2 activation, TG and cholesterol accumulation, as well as MASH progression, all depend on Casp2 [91].”
From Hepatic Insulin Resistance and Steatosis in Metabolic Dysfunction-Associated Steatotic Liver Disease: New Insights into Mechanisms and Clinical Implications (2025) · cites this paper as [91]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Improved vectors and genome-wide libraries for CRISPR screening
Sanjana, N. E., Shalem, O., & Zhang, F. (2014) · Nature Methods · doi:10.1038/nmeth.3047 · Cited by 5,239 · see citing works
Obesity induces a phenotypic switch in adipose tissue macrophage polarization
Lumeng, C. N., Bodzin, J. L., & Saltiel, A. R. (2007) · Journal of Clinical Investigation · doi:10.1172/jci29881 · Cited by 4,664 · see citing works
Self-citationBrown, M. S., & Goldstein, J. L. (1997) · Cell · doi:10.1016/s0092-8674(00)80213-5 · Cited by 3,834 · see citing works
Evolution of inflammation in nonalcoholic fatty liver disease: The multiple parallel hits hypothesis
Tilg, H., & Moschen, A. R. (2010) · Hepatology · doi:10.1002/hep.24001 · Cited by 2,548 · see citing works
Human Fatty Liver Disease: Old Questions and New Insights
Cohen, J. C., Horton, J. D., & Hobbs, H. H. (2011) · Science · doi:10.1126/science.1204265 · Cited by 2,089 · see citing works
A lipidomic analysis of nonalcoholic fatty liver disease
Puri, P., Baillie, R. A., Wiest, M. M., Mirshahi, F., Choudhury, J., Cheung, O., Sargeant, C., Contos, M. J., & Sanyal, A. J. (2007) · Hepatology · doi:10.1002/hep.21763 · Cited by 1,338 · see citing works
Feldmann, H. M., Golozoubova, V., Cannon, B., & Nedergaard, J. (2009) · Cell Metabolism · doi:10.1016/j.cmet.2008.12.014 · Cited by 1,318 · see citing works
Loomba, R., Seguritan, V., Li, W., Long, T., Klitgord, N., Bhatt, A., Dulai, P. S., Caussy, C., Bettencourt, R., Highlander, S. K., et al. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.04.001 · Cited by 1,123 · see citing works
Self-citationLambert, J. E., Ramos–Roman, M. A., Browning, J. D., & Parks, E. J. (2014) · Gastroenterology · doi:10.1053/j.gastro.2013.11.049 · Cited by 1,069 · cited 1× · see citing works
“One metabolic process thought to initiate NAFLD is de novo lipogenesis (DNL), whose rate is up to 3-fold higher in NAFLD patients (Lambert et al., 2014).”
Regulation of Hepatic Lipogenesis by the Transcription Factor XBP1
Lee, A., Scapa, E. F., Cohen, D. E., & Glimcher, L. H. (2008) · Science · doi:10.1126/science.1158042 · Cited by 978 · see citing works
Substrate Specificities of Caspase Family Proteases
Talanian, R. V., Quinlan, C., Trautz, S., Hackett, M. C., Mankovich, J. A., Banach, D. L., Ghayur, T., Brady, K. D., & Wong, W. W. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.15.9677 · Cited by 879 · see citing works
Park, C. C., Nguyen, P., Hernandez, C., Bettencourt, R., Ramirez, K., Fortney, L., Hooker, J. C., Sy, E. Z., Savides, M. T., Alquiraish, M. H., et al. (2016) · Gastroenterology · doi:10.1053/j.gastro.2016.10.026 · Cited by 715 · see citing works
Self-citationYecies, J. L., Zhang, H., Menon, S., Liu, S., Yecies, D. W., Lipovsky, A. I., Görgün, C. Z., Kwiatkowski, D. J., Hotamışlıgil, G. S., Lee, C., et al. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.06.002 · Cited by 662 · see citing works
IRE1α Cleaves Select microRNAs During ER Stress to Derepress Translation of Proapoptotic Caspase-2
Upton, J.-P., Wang, L., Han, D., Wang, E. S., Huskey, N. E., Lim, L., Truitt, M., McManus, M. T., Ruggero, D., Goga, A., et al. (2012) · Science · doi:10.1126/science.1226191 · Cited by 640 · see citing works
Mitochondrial free cholesterol loading sensitizes to TNF- and Fas-mediated steatohepatitis
Marı́, M., Caballero, F. G., Colell, A., Morales, A., Caballería, J., Fernandez, A., Enrich, C., Fernández-Checa, J. C., & García‐Ruiz, C. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2006.07.006 · Cited by 605 · see citing works
ER Stress Cooperates with Hypernutrition to Trigger TNF-Dependent Spontaneous HCC Development
Nakagawa, H., Umemura, A., Taniguchi, K., Font-Burgada, J., Dhar, D., Ogata, H., Zhong, Z., Valasek, M. A., Seki, E., Hidalgo, J., et al. (2014) · Cancer Cell · doi:10.1016/j.ccr.2014.07.001 · Cited by 525 · see citing works
Self-citationUnsaturated Fatty Acids Down-regulate SREBP Isoforms 1a and 1c by Two Mechanisms in HEK-293 Cells
Hannah, V. C., Ou, J., Luong, A., Goldstein, J. L., & Brown, M. S. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m007273200 · Cited by 448 · see citing works
Oyadomari, S., Harding, H. P., Zhang, Y., Oyadomari, M., & Ron, D. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2008.04.011 · Cited by 431 · see citing works
Sakai, J., Rawson, R. B., Espenshade, P. J., Cheng, D., Seegmiller, A. C., Goldstein, J. L., & Brown, M. S. (1998) · Molecular Cell · doi:10.1016/s1097-2765(00)80150-1 · Cited by 405 · see citing works
NASH is an Infl ammatory Disorder: Pathogenic, Prognostic and Therapeutic Implications
Farrell, G. C., Rooyen, D. M. V., Gan, L. T., & Chitturi, S. (2012) · Gut and Liver · doi:10.5009/gnl.2012.6.2.149 · Cited by 400 · see citing works
Caspase-2 Is Localized at the Golgi Complex and Cleaves Golgin-160 during Apoptosis
Mancini, M., Machamer, C. E., Roy, S., Nicholson, D. W., Thornberry, N. A., Casciola-Rosen, L. A., & Rosen, A. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.149.3.603 · Cited by 379 · see citing works
The unfolded protein response transducer IRE1α prevents ER stress‐induced hepatic steatosis
Zhang, K., Wang, S., Malhotra, J. D., Hassler, J. R., Back, S. H., Wang, G., Chang, L., Xu, W., Miao, H. Z., Leonardi, R., et al. (2011) · The EMBO Journal · doi:10.1038/emboj.2011.52 · Cited by 368 · see citing works
Self-citationEnhanced free cholesterol, SREBP-2 and StAR expression in human NASH
Caballero, F., Fernández, A., De Lacy, A. M., Fernández-Checa, J. C., Caballería, J., & García-Ruiz, C. (2009) · Journal of Hepatology · doi:10.1016/j.jhep.2008.12.016 · Cited by 368 · see citing works
Loomba, R. S., Sirlin, C. B., Ang, B., Bettencourt, R., Jain, R., Salotti, J., Soaft, L., Hooker, J. C., Kono, Y., Bhatt, A., et al. (2014) · Hepatology · doi:10.1002/hep.27647 · Cited by 346 · see citing works
Self-citationAnimal models of NASH: Getting both pathology and metabolic context right
Larter, C. Z., & Yeh, M. M. (2008) · Journal of Gastroenterology and Hepatology · doi:10.1111/j.1440-1746.2008.05543.x · Cited by 337 · see citing works
Transport-Dependent Proteolysis of SREBP
DeBose‐Boyd, R. A., Brown, M. S., Li, W., Nohturfft, A., Goldstein, J. L., & Espenshade, P. J. (1999) · Cell · doi:10.1016/s0092-8674(00)81668-2 · Cited by 326 · see citing works
Cleavage of sterol regulatory element binding proteins (SREBPs) by CPP32 during apoptosis.
Wang, X., Zelenski, N. G., Yang, J., Sakai, J., Brown, M. S., & Goldstein, J. L. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00438.x · Cited by 313 · see citing works
Role of endoplasmic reticulum stress in the pathogenesis of nonalcoholic fatty liver disease
Zhang, X.-Q. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i7.1768 · Cited by 290 · see citing works
Insulin stimulation of SREBP-1c processing in transgenic rat hepatocytes requires p70 S6-kinase
Owen, J., Zhang, Y., Bae, S., Farooqi, M., Liang, G., Hammer, R., Goldstein, J., & Brown, M. S. (2012) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1213343109 · Cited by 276 · see citing works
Osborne, T. F., & Espenshade, P. J. (2009) · Genes & Development · doi:10.1101/gad.1854309 · Cited by 264 · see citing works
Bobrovnikova-Marjon, E. V., Hatzivassiliou, G., Grigoriadou, C., Romero, M., Cavener, D. R., Thompson, C. B., & Diehl, J. A. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808517105 · Cited by 262 · see citing works
Lodhi, I. J., Yin, L., Jensen-Urstad, A. P. L., Funai, K., Coleman, T., Baird, J. H., Ramahi, M. K. E., Razani, B., Song, H., Hsu, F., et al. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.06.013 · Cited by 245 · see citing works
Le, T., Chen, J., Changchien, C., Peterson, M. R., Kono, Y., Patton, H. M., Cohen, B. L., Brenner, D. A., Sirlin, C. B., & Loomba, R. S. (2012) · Hepatology · doi:10.1002/hep.25731 · Cited by 244 · see citing works
Self-citationDecreased lipid synthesis in livers of mice with disrupted Site-1 protease gene
Yang, J., Goldstein, J. L., Hammer, R. E., Moon, Y.-A., Brown, M. S., & Horton, J. D. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.201524598 · Cited by 237 · see citing works
ATF6 modulates SREBP2‐mediated lipogenesis
Zeng, L., Lu, M. M., Mori, K., Luo, S. D., Lee, A. S., Zhu, Y., & Shyy, J. Y. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600106 · Cited by 218 · see citing works
Animal Models of Nonalcoholic Steatohepatitis: Eat, Delete, and Inflame
Ibrahim, S. H., Hirsova, P., Malhi, H., & Gores, G. J. (2016) · Digestive Diseases and Sciences · doi:10.1007/s10620-015-3977-1 · Cited by 218 · see citing works
O’Reilly, L. A., Ekert, P. G., Harvey, N. L., Marsden, V. S., Cullen, L., Vaux, D. L., Häcker, G. A., Magnusson, C., Pakusch, M., Cecconi, F., et al. (2002) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401033 · Cited by 191 · see citing works
Lee, J. N., & Ye, J. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m408235200 · Cited by 186 · see citing works
Espenshade, P. J., Cheng, D., Goldstein, J. L., & Brown, M. S. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.32.22795 · Cited by 179 · see citing works
ER stress: Can the liver cope?
Ji, C., & Kaplowitz, N. (2006) · Journal of Hepatology · doi:10.1016/j.jhep.2006.06.004 · Cited by 171 · see citing works
Nonalcoholic fatty liver disease with cirrhosis increases familial risk for advanced fibrosis
Caussy, C., Soni, M., Cui, J. Y., Bettencourt, R., Schork, N. J., Chen, C., Ikhwan, M., Bassirian, S., Cepin, S., Gonzalez, M. P., et al. (2017) · Journal of Clinical Investigation · doi:10.1172/jci93465 · Cited by 166 · see citing works
Self-citationHepatocyte Transplantation into Diseased Mouse Liver
Weglarz, T. C., Degen, J. L., & Sandgren, E. P. (2000) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)64835-3 · Cited by 149 · see citing works
The enigma of caspase-2: the laymen's view
Krumschnabel, G., Sohm, B., Bock, F. J., Manzl, C., & Villunger, A. (2008) · Cell Death and Differentiation · doi:10.1038/cdd.2008.170 · Cited by 122 · see citing works
Bouchier‐Hayes, L., & Green, D. R. (2011) · Cell Death and Differentiation · doi:10.1038/cdd.2011.157 · Cited by 110 · see citing works
Machado, M. V., Michelotti, G. A., Pereira, T. A., Boursier, J., Krüger, L., Swiderska‐Syn, M., Karaca, G., Xie, G., Guy, C. D., Bohinc, B. N., et al. (2014) · Gut · doi:10.1136/gutjnl-2014-307362 · Cited by 102 · see citing works
Cheung, H. H., Kelly, N. L., Liston, P., & Korneluk, R. G. (2006) · Experimental Cell Research · doi:10.1016/j.yexcr.2006.03.027 · Cited by 101 · see citing works
Endoplasmic reticulum stress and lipid dysregulation
Colgan, S. M., Al‐Hashimi, A., & Austin, R. C. (2011) · Expert Reviews in Molecular Medicine · doi:10.1017/s1462399410001742 · Cited by 98 · see citing works
Croze, E. M., & Morré, D. J. (1984) · Journal of Cellular Physiology · doi:10.1002/jcp.1041190109 · Cited by 91 · see citing works
Cheng, D., Espenshade, P. J., Slaughter, C. A., Jaén, J. C., Brown, M. S., & Goldstein, J. L. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.32.22805 · Cited by 79 · see citing works
A novel automated image analysis method for accurate adipocyte quantification
Osman, O. S., Selway, J. L., Kępczyńska, M. A., Stocker, C. J., O’Dowd, J. F., Cawthorne, M. A., Arch, J. R. S., Jassim, S., & Langlands, K. (2013) · Adipocyte · doi:10.4161/adip.24652 · Cited by 64 · see citing works
ER stress does not cause upregulation and activation of caspase-2 to initiate apoptosis
Sandow, J. J., Dorstyn, L., O’Reilly, L. A., Tailler, M., Kumar, S., Strasser, A., & Ekert, P. G. (2013) · Cell Death and Differentiation · doi:10.1038/cdd.2013.168 · Cited by 56 · see citing works
Caspase-2, a Novel Lipid Sensor under the Control of Sterol Regulatory Element Binding Protein 2
Logette, E., Jossic-Corcos, C. L., Masson, D., Solier, S., Sequeira-Legrand, A., Dugail, I., Lemaire‐Ewing, S., Desoche, L., Solary, É., & Corcos, L. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.21.9621-9631.2005 · Cited by 52 · see citing works
A Modified Urokinase Plasminogen Activator Induces Liver Regeneration Without Bleeding
Lieber, A., Peeters, M.-J. T. F. D. V., Gown, A. M., Perkins, J. D., & Kay, M. A. (1995) · Human Gene Therapy · doi:10.1089/hum.1995.6.8-1029 · Cited by 50 · see citing works
DNA rearrangement causes hepatocarcinogenesis in albumin-plasminogen activator transgenic mice.
Sandgren, E. P., Palmiter, R. D., Heckel, J. L., Brinster, R. L., & Degen, J. L. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.23.11523 · Cited by 41 · see citing works
Liver cholesterol: is it playing possum in NASH?
Farrell, G. C., & Rooyen, D. M. V. (2012) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00008.2012 · Cited by 41 · see citing works
Pastorino, J. G., & Shulga, N. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m800237200 · Cited by 24 · see citing works
Characterization of the Human Insulin-induced Gene 2 (INSIG2) Promoter
Fernández-Álvarez, A. J., Álvarez, M. S., Cucarella, C., & Casado, M. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.067447 · Cited by 23 · see citing works
Zymogen Activation and Subcellular Activity of Subtilisin Kexin Isozyme 1/Site 1 Protease
da Palma, J. R., Burri, D. J., Oppliger, J., Salamina, M., Cendron, L., de Laureto, P. P., Seidah, N. G., Kunz, S., & Pasquato, A. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.588525 · Cited by 22 · see citing works
Activation of Sterol Regulatory Element-binding Protein by the Caspase Drice in Drosophila Larvae
Amarneh, B., Matthews, K. A., & Rawson, R. B. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m900346200 · Cited by 22 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Molecular and cellular mechanisms of liver fibrosis and its regression
Kisseleva, T., & Brenner, D. (2021) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-020-00372-7 · Cited by 2,024 · see citing works
Mechanisms and disease consequences of nonalcoholic fatty liver disease
Loomba, R., Friedman, S. L., & Shulman, G. I. (2021) · Cell · doi:10.1016/j.cell.2021.04.015 · Cited by 2,002 · see citing works
Self-citationMechanisms of Fibrosis Development in Nonalcoholic Steatohepatitis
Schwabe, R. F., Tabas, I., & Pajvani, U. B. (2020) · Gastroenterology · doi:10.1053/j.gastro.2019.11.311 · Cited by 671 · see citing works
Immune cell-mediated features of non-alcoholic steatohepatitis
Huby, T., & Gautier, E. L. (2022) · Nature Reviews Immunology · doi:10.1038/s41577-021-00639-3 · Cited by 573 · see citing works
Bile acid receptors FXR and TGR5 signaling in fatty liver diseases and therapy
Chiang, J. Y. L., & Ferrell, J. M. (2020) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00223.2019 · Cited by 580 · see citing works
Pharmacological targeting of endoplasmic reticulum stress in disease
Marciniak, S. J., Chambers, J. E., & Ron, D. (2021) · Nature Reviews Drug Discovery · doi:10.1038/s41573-021-00320-3 · Cited by 536 · see citing works
Non-alcoholic fatty liver disease: the interplay between metabolism, microbes and immunity
Tilg, H., Adolph, T., Dudek, M., & Knolle, P. (2021) · Nature Metabolism · doi:10.1038/s42255-021-00501-9 · Cited by 495 · see citing works
Insulin signaling in health and disease
Saltiel, A. R. (2021) · Journal of Clinical Investigation · doi:10.1172/jci142241 · Cited by 446 · see citing works
Self-citationRole of Insulin Resistance in MAFLD
Sakurai, Y., Kubota, N., Yamauchi, T., & Kadowaki, T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22084156 · Cited by 448 · see citing works
Metabolic reprogramming in liver fibrosis
Horn, P., & Tacke, F. (2024) · Cell Metabolism · doi:10.1016/j.cmet.2024.05.003 · Cited by 432 · see citing works
Endoplasmic reticulum stress in liver diseases
Ajoolabady, A., Kaplowitz, N., Lebeaupin, C., Kroemer, G., Kaufman, R. J., Malhi, H., & Ren, J. T. (2022) · Hepatology · doi:10.1002/hep.32562 · Cited by 410 · see citing works
Self-citationA new perspective on NAFLD: Focusing on lipid droplets
Scorletti, E., & Carr, R. M. (2021) · Journal of Hepatology · doi:10.1016/j.jhep.2021.11.009 · Cited by 376 · see citing works
Apoptotic cell death in disease—Current understanding of the NCCD 2023
Vitale, I., Pietrocola, F., Guilbaud, E., Aaronson, S. A., Abrams, J., Adam, D., Agostini, M., Agostinis, P., Alnemri, E. S., Altucci, L., et al. (2023) · Cell Death and Differentiation · doi:10.1038/s41418-023-01153-w · Cited by 359 · see citing works
Fructose stimulated de novo lipogenesis is promoted by inflammation
Todoric, J., Di Caro, G., Reibe, S., Henstridge, D. C., Green, C. R., Vrbanac, A., Ceteci, F., Conche, C., McNulty, R., Shalapour, S., et al. (2020) · Nature Metabolism · doi:10.1038/s42255-020-0261-2 · Cited by 328 · see citing works
Self-citationCholesterol-induced toxicity: An integrated view of the role of cholesterol in multiple diseases
Song, Y., Liu, J., Zhao, K. Z., Gao, L., & Zhao, J. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.09.001 · Cited by 325 · see citing works
An AMPK–caspase-6 axis controls liver damage in nonalcoholic steatohepatitis
Zhao, P., Sun, X., Chaggan, C., Liao, Z., Wong, K. I., He, F., Singh, S., Loomba, R. S., Karin, M., Witztum, J. L., et al. (2020) · Science · doi:10.1126/science.aay0542 · Cited by 308 · see citing works
Self-citationHigh fat diet-triggered non-alcoholic fatty liver disease: A review of proposed mechanisms
Lian, C.-Y., Zhai, Z., Li, Z., & Wang, L. (2020) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2020.109199 · Cited by 304 · see citing works
Molecular aspects of fructose metabolism and metabolic disease
Herman, M. A., & Birnbaum, M. J. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.09.010 · Cited by 298 · see citing works
Hou, J., Zhang, J., Cui, P., Zhou, Y., Liu, C., Wu, X., Ji, Y., Wang, S., Cheng, B., Ye, H., et al. (2021) · Journal of Clinical Investigation · doi:10.1172/jci135197 · Cited by 239 · see citing works
Liver fibrosis in NAFLD/NASH: from pathophysiology towards diagnostic and therapeutic strategies
Parola, M., & Pinzani, M. (2023) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2023.101231 · Cited by 226 · see citing works
Ma, H.-Y., Yamamoto, G., Xu, J., Liu, X., Karin, D., Kim, J. Y., Alexandrov, L. B., Koyama, Y., Nishio, T., Benner, C., et al. (2020) · Journal of Hepatology · doi:10.1016/j.jhep.2019.12.016 · Cited by 216 · see citing works
Self-citationCholesterol Stabilizes TAZ in Hepatocytes to Promote Experimental Non-alcoholic Steatohepatitis
Wang, X., Cai, B., Yang, X., Sonubi, O. O., Zheng, Z., Ramakrishnan, R., Shi, H., Valenti, L., Pajvani, U. B., Sandhu, J., et al. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.03.010 · Cited by 204 · see citing works
A long way to go: caspase inhibitors in clinical use
Dhani, S., Zhao, Y., & Zhivotovsky, B. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-04240-3 · Cited by 200 · see citing works
“Sweet death”: Fructose as a metabolic toxin that targets the gut-liver axis
Febbraio, M. A., & Karin, M. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.09.004 · Cited by 177 · see citing works
Self-citationSREBP-1c and lipogenesis in the liver: an update
Ferré, P., Phan, F., & Foufelle, F. (2021) · Biochemical Journal · doi:10.1042/bcj20210071 · Cited by 168 · see citing works
Oxidative Stress in NAFLD: Role of Nutrients and Food Contaminants
Rives, C., Fougerat, A., Ellero‐Simatos, S., Loiseau, N., Guillou, H., Gamet‐Payrastre, L., & Wahli, W. (2020) · Biomolecules · doi:10.3390/biom10121702 · Cited by 160 · see citing works
TMEM41B acts as an ER scramblase required for lipoprotein biogenesis and lipid homeostasis
Huang, D., Xu, B., Liu, L., Wu, L., Zhu, Y., Ghanbarpour, A., Wang, Y., Chen, F., Lyu, J., Hu, Y., et al. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.05.006 · Cited by 157 · see citing works
Fan, Y., & Simmen, T. (2019) · Cells · doi:10.3390/cells8091071 · Cited by 141 · see citing works
Yahoo, N., Dudek, M., Knolle, P. A., & Heikenwälder, M. F. (2023) · Journal of Hepatology · doi:10.1016/j.jhep.2023.02.033 · Cited by 145 · see citing works
SREBP Regulation of Lipid Metabolism in Liver Disease, and Therapeutic Strategies
Li, N., Li, X., Ding, Y., Liu, X., Diggle, K., Kisseleva, T., & Brenner, D. A. (2023) · Biomedicines · doi:10.3390/biomedicines11123280 · Cited by 140 · see citing works
Immunopathobiology and therapeutic targets related to cytokines in liver diseases
He, Y., Hwang, S., Ahmed, Y. A., Feng, D., Li, N., Ribeiro, M. D. C., Lafdil, F., Kisseleva, T., Szabó, G., & Gao, B. (2020) · Cellular and Molecular Immunology · doi:10.1038/s41423-020-00580-w · Cited by 136 · see citing works
Danger signals in liver injury and restoration of homeostasis
Han, H., Desert, R., Das, S., Song, Z., Athavale, D., Ge, X., & Nieto, N. (2020) · Journal of Hepatology · doi:10.1016/j.jhep.2020.04.033 · Cited by 127 · see citing works
Wei, S., Qiu, T., Wang, N., Yao, X., Jiang, L., Jia, X., Tao, Y., Zhang, J., Zhu, Y., Yang, G., et al. (2020) · Environmental Research · doi:10.1016/j.envres.2020.109824 · Cited by 121 · see citing works
FOXA3 induction under endoplasmic reticulum stress contributes to non-alcoholic fatty liver disease
Liu, C., Zhou, B., Meng, M., Zhao, W., Wang, D., Yuan, Y., Zheng, Y. F., Qiu, J. F., Li, Y., Li, G., et al. (2021) · Journal of Hepatology · doi:10.1016/j.jhep.2021.01.042 · Cited by 119 · see citing works
Kawamura, S., Matsushita, Y., Kurosaki, S., Tange, M., Fujiwara, N., Hayata, Y., Hayakawa, Y., Suzuki, N., Hata, M., Tsuboi, M., et al. (2022) · Journal of Clinical Investigation · doi:10.1172/jci151895 · Cited by 115 · see citing works
Podszun, M. C., Alawad, A. S., Lingala, S., Morris, N., Huang, W. A., Yang, S. B., Schoenfeld, M., Rolt, A., Ouwerkerk, R., Valdez, K., et al. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101710 · Cited by 115 · see citing works
de la Rosa, L. C., García‐Ruiz, C., Vallejo, C., Baulies, A., Núñez, S., Monte, M. J., Marı́n, J. J. G., Baila-Rueda, L., Cenarro, A., Civeira, F., et al. (2021) · Journal of Hepatology · doi:10.1016/j.jhep.2021.01.028 · Cited by 101 · see citing works
Self-citationKanda, T., Goto, T., Hirotsu, Y., Masuzaki, R., Moriyama, M., & Omata, M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21041525 · Cited by 95 · see citing works
Zhou, Y., Li, P., Wang, X., Wu, C., Fan, N., Liu, X., Wu, L., Zhang, W., Zhang, W., Liu, Z., et al. (2020) · Chemical Science · doi:10.1039/d0sc02922j · Cited by 90 · see citing works
The metabolic basis of nonalcoholic steatohepatitis
Chakravarthy, M. V., & Neuschwander‐Tetri, B. A. (2020) · Endocrinology Diabetes & Metabolism · doi:10.1002/edm2.112 · Cited by 87 · see citing works
Truong, X. T., & Lee, D. H. (2025) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2025.0644 · Cited by 84 · see citing works
“A study showed that ER-stress-me-diated SREBP1/2 activation, TG and cholesterol accumulation, as well as MASH progression, all depend on Casp2 [91].”
Donné, R., Saroul-Aïnama, M., Cordier, P., Hammoutène, A., Kaboré, C., Stadler, M., Nemazanyy, I., Galy–Fauroux, I., Herrag, M., Riedl, T., et al. (2022) · Developmental Cell · doi:10.1016/j.devcel.2022.06.003 · Cited by 81 · see citing works
P53 deficiency affects cholesterol esterification to exacerbate hepatocarcinogenesis
Zhu, Y., Gu, L., Lin, X., Zhou, X., Lu, B., Liu, C., Li, Y., Prochownik, E. V., Karin, M., Wang, X., et al. (2022) · Hepatology · doi:10.1002/hep.32518 · Cited by 78 · see citing works
Self-citationLi, S., Li, X., Chen, F., Liu, M., Ning, L., Yan, Y.-F., Zhang, S., Huang, S., & Tu, C. (2021) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2021.108888 · Cited by 73 · see citing works
Endoplasmic Reticulum Stress Signaling and the Pathogenesis of Hepatocarcinoma
Wei, J., & Fang, D. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041799 · Cited by 69 · see citing works
Sladky, V. C., Knapp, K., Soratroi, C., Heppke, J., Eichin, F., Rocamora-Reverte, L., Szabo, T., Bongiovanni, L., Westendorp, B., Moreno, E., et al. (2020) · Developmental Cell · doi:10.1016/j.devcel.2019.12.016 · Cited by 55 · see citing works
The role of exosomal miRNA in nonalcoholic fatty liver disease
Mahmoudi, A. A., Butler, A. E., Jamialahmadi, T., & Sahebkar, A. (2022) · Journal of Cellular Physiology · doi:10.1002/jcp.30699 · Cited by 65 · see citing works
El-Derany, M. O., & AbdelHamid, S. G. (2021) · Biochemical Pharmacology · doi:10.1016/j.bcp.2021.114624 · Cited by 64 · see citing works
Regulation of Hepatic Stellate Cell Phenotypes in Metabolic Dysfunction–Associated Steatohepatitis
Kisseleva, T., Ganguly, S., Murad, R., Wang, A., & Brenner, D. A. (2025) · Gastroenterology · doi:10.1053/j.gastro.2025.03.010 · Cited by 72 · see citing works
The Origin and Fate of Liver Myofibroblasts
Kim, H. Y., Sakane, S., Eguileor, A., Carvalho Gontijo Weber, R., Lee, W., Liu, X., Lam, K., Ishizuka, K., Rosenthal, S. B., Diggle, K., et al. (2024) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2023.09.008 · Cited by 63 · see citing works
Tak, J., Kim, Y. S., Kim, T. H., Park, G., Hwang, S., & Kim, S. G. (2022) · Theranostics · doi:10.7150/thno.67722 · Cited by 63 · see citing works
Decoding inflammation, its causes, genomic responses, and emerging countermeasures
Hawiger, J., & Zienkiewicz, J. (2019) · Scandinavian Journal of Immunology · doi:10.1111/sji.12812 · Cited by 62 · see citing works
Hepatocyte Injury and Hepatic Stem Cell Niche in the Progression of Non-Alcoholic Steatohepatitis
Overi, D., Carpino, G., Franchitto, A., Onori, P., & Gaudio, E. (2020) · Cells · doi:10.3390/cells9030590 · Cited by 61 · see citing works
Caspase-2 Substrates: To Apoptosis, Cell Cycle Control, and Beyond
Brown-Suedel, A. N., & Bouchier‐Hayes, L. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.610022 · Cited by 58 · see citing works
Endoplasmic reticulum stress sensor IRE1α propels neutrophil hyperactivity in lupus
Sule, G. J., Abuaita, B. H., Steffes, P. A., Fernandes, A. T., Estes, S. K., Dobry, C. J., Pandian, D., Gudjonsson, J. E., Kahlenberg, J. M., O’Riordan, M. X., et al. (2021) · Journal of Clinical Investigation · doi:10.1172/jci137866 · Cited by 60 · see citing works
Interleukin-17 in Liver Disease Pathogenesis
Li, N., Yamamoto, G., Fuji, H., & Kisseleva, T. (2021) · Seminars in Liver Disease · doi:10.1055/s-0041-1730926 · Cited by 64 · see citing works
Endoplasmic reticulum stress in diseases
Liu, Y., Xu, C., Gu, R., Han, R., Li, Z., & Xu, X. (2024) · MedComm · doi:10.1002/mco2.701 · Cited by 67 · see citing works
Jia, H., Liu, J., Fang, T., Zhou, Z. D., Li, R., Yin, W., Qian, Y., Wang, Q., Zhou, W., Liu, C., et al. (2023) · Science Advances · doi:10.1126/sciadv.abq2937 · Cited by 58 · see citing works
Ali, E. S., Rychkov, G. Y., & Barritt, G. J. (2019) · Cell Calcium · doi:10.1016/j.ceca.2019.102057 · Cited by 58 · see citing works
Reprogramming of Hepatic Metabolism and Microenvironment in Nonalcoholic Steatohepatitis
Rui, L., & Lin, J. D. (2022) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-062220-105200 · Cited by 56 · see citing works
Jiang, S., Yang, X., Yang, Z., Li, J., Xu, M., Qu, Y.-X., Tang, J., Li, Y., Wang, L., Shao, Y., et al. (2022) · Hepatology · doi:10.1002/hep.32381 · Cited by 56 · see citing works
Treating inflammation to combat non-alcoholic fatty liver disease
Wiering, L., & Tacke, F. (2022) · Journal of Endocrinology · doi:10.1530/joe-22-0194 · Cited by 58 · see citing works
Animal Models of Fibrosis in Nonalcoholic Steatohepatitis: Do They Reflect Human Disease?
Ipsen, D. H., Lykkesfeldt, J., & Tveden-Nyborg, P. (2020) · Advances in Nutrition · doi:10.1093/advances/nmaa081 · Cited by 51 · see citing works
The p53-caspase-2 axis in the cell cycle and DNA damage response
Lim, Y. P., Dorstyn, L., & Kumar, S. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00590-2 · Cited by 56 · see citing works
Overcoming enzalutamide resistance in metastatic prostate cancer by targeting sphingosine kinase
Lin, H., Mak, B., Yeung, N. K., Huynh, K., Meikle, T. G., Mellett, N. A., Kwan, E. M., Fettke, H., Tran, B., Davis, I. D., et al. (2021) · EBioMedicine · doi:10.1016/j.ebiom.2021.103625 · Cited by 55 · see citing works
Zhou, Y., Liu, Z., Qiao, G., Tang, B., & Li, P. (2021) · Chinese Chemical Letters · doi:10.1016/j.cclet.2021.04.035 · Cited by 54 · see citing works
p62/SQSTM1 in liver diseases: the usual suspect with multifarious identities
Tan, C. T., Soh, N. J. H., Chang, H., & Yu, V. C. K. (2021) · FEBS Journal · doi:10.1111/febs.16317 · Cited by 52 · see citing works
Fowler, J. W., Zhang, R., Tao, B., Boutagy, N. E., & Sessa, W. C. (2022) · eLife · doi:10.7554/elife.79529 · Cited by 51 · see citing works
Mollica, G., Senesi, P., Codella, R., Vacante, F., Montesano, A., Luzi, L., & Terruzzi, I. M. (2019) · Digestive and Liver Disease · doi:10.1016/j.dld.2019.09.002 · Cited by 52 · see citing works
Transcriptional Regulation in Non-Alcoholic Fatty Liver Disease
Steensels, S., Qiao, J., & Ersoy, B. A. (2020) · Metabolites · doi:10.3390/metabo10070283 · Cited by 51 · see citing works
MITOCHONDRIAL CHOLESTEROL AND CANCER
García‐Ruiz, C., de la Rosa, L. C., Ribas, V., & Fernández-Checa, J. C. (2020) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2020.07.014 · Cited by 52 · see citing works
PIDDosome‐induced p53‐dependent ploidy restriction facilitates hepatocarcinogenesis
Sladky, V. C., Knapp, K., Szabo, T., Braun, V. Z., Bongiovanni, L., van den Bos, H., Spierings, D., Westendorp, B., Curinha, A., Stojaković, T., et al. (2020) · EMBO Reports · doi:10.15252/embr.202050893 · Cited by 43 · see citing works
Li, C., Cai, C., Wang, C., Chen, X., Zhang, B., & Huang, Z. (2024) · Clinical and Molecular Hepatology · doi:10.3350/cmh.2024.0857 · Cited by 56 · see citing works
Morgan, P. K., Fang, L., Lancaster, G. I., & Murphy, A. J. (2019) · Journal of Lipid Research · doi:10.1194/jlr.tr119000267 · Cited by 49 · see citing works
Rao, S., Yang, X., Ohshiro, K., Zaidi, S., Wang, Z., Shetty, K., Xiang, X., Hassan, M. I., Mohammad, T., Latham, P. S., et al. (2021) · Science Translational Medicine · doi:10.1126/scitranslmed.abk2267 · Cited by 47 · see citing works
Samy, A. M., Kandeil, M. A., Sabry, D., Abdel-Ghany, A. A., & Mahmoud, M. O. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e30387 · Cited by 50 · see citing works
Antifibrotic therapies for metabolic dysfunction-associated steatotic liver disease
Schwabe, R. F., Tacke, F., Sugimoto, A., & Friedman, S. L. (2025) · JHEP Reports · doi:10.1016/j.jhepr.2025.101421 · Cited by 50 · see citing works
Eilam, Y., Pintel, N., Khattib, H., Shagug, N., Taha, R., & Avni, D. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232213667 · Cited by 48 · see citing works
Uncovering the PIDDosome and caspase-2 as regulators of organogenesis and cellular differentiation
Sladky, V. C., & Villunger, A. (2020) · Cell Death and Differentiation · doi:10.1038/s41418-020-0556-6 · Cited by 39 · see citing works
NIRANJAN, S., Phillips, B. E., & Giannoukakis, N. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1193373 · Cited by 43 · see citing works
Phospholipid Membrane Transport and Associated Diseases
Ventura, R., Martínez-Ruíz, I., & Hernández‐Álvarez, M. I. (2022) · Biomedicines · doi:10.3390/biomedicines10051201 · Cited by 42 · see citing works
JMJD4-demethylated RIG-I prevents hepatic steatosis and carcinogenesis
Li, Z., Zhou, Y., Jia, K., Yang, Y., Zhang, L., Wang, S., Dong, Y., Wang, M., Li, Y., Lu, S., et al. (2022) · Journal of Hematology & Oncology · doi:10.1186/s13045-022-01381-6 · Cited by 42 · see citing works
Gu, L., Zhu, Y., Watari, K., Lee, M., Liu, J., Perez, S., Thai, M., Mayfield, J. E., Zhang, B., Rocha, K. C. E., et al. (2023) · Cell Metabolism · doi:10.1016/j.cmet.2023.03.021 · Cited by 43 · see citing works
Self-citationKuan, Y.-C., Takahashi, Y., Maruyama, T., Shimizu, M., Yamauchi, Y., & Sato, R. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.011849 · Cited by 41 · see citing works
Endoplasmic Reticulum Stress in Biological Processing and Disease
Köksal, A. R., Verne, G. N., & Zhou, Q. (2021) · Journal of Investigative Medicine · doi:10.1136/jim-2020-001570 · Cited by 41 · see citing works
Shin, S., You, I., Jeong, M., Bae, Y., Wang, X., Cawley, M. L., Han, A., & Lim, B. K. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01208-0 · Cited by 40 · see citing works
Unfolded Protein Response Signaling in Liver Disorders: A 2023 Updated Review
Shreya, S., Grosset, C. F., & Jain, B. P. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241814066 · Cited by 41 · see citing works
Kisseleva, T., & Brenner, D. A. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.10.010 · Cited by 39 · see citing works
MASH as an emerging cause of hepatocellular carcinoma: current knowledge and future perspectives
Karin, M., & Kim, J. Y. (2024) · Molecular Oncology · doi:10.1002/1878-0261.13685 · Cited by 43 · see citing works
Self-citationBarbhuiya, P. A., Yoshitomi, R., & Pathak, M. P. (2025) · Current Obesity Reports · doi:10.1007/s13679-025-00626-y · Cited by 38 · see citing works
Deng, X., Ye, Z., Cao, H., Bai, Y., Che, Q., Guo, J., & Su, Z. (2020) · Food & Function · doi:10.1039/d0fo01107j · Cited by 38 · see citing works
Li, R., Li, Y., Yang, X., Yu, H., Yu, H., & Li, Y. (2022) · Journal of Translational Medicine · doi:10.1186/s12967-022-03540-2 · Cited by 38 · see citing works
ACMSD inhibition corrects fibrosis, inflammation, and DNA damage in MASLD/MASH
Liu, Y. J., Kimura, M., Li, X., Sulc, J., Wang, Q., Rodríguez-López, S., Scantlebery, A. M. L., Strotjohann, K., Gallart‐Ayala, H., Vijayakumar, A., et al. (2024) · Journal of Hepatology · doi:10.1016/j.jhep.2024.08.009 · Cited by 37 · see citing works
Angelini, G., Castagneto‐Gissey, L., Salinari, S., BERTUZZI, A., Anello, D., Pradhan, M., Zschätzsch, M., Ritter, P., le Roux, C. W., Rubino, F., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-35310-5 · Cited by 36 · see citing works
Multi-walled carbon nanotubes promoted lipid accumulation in human aortic smooth muscle cells
Yang, H., Li, J., Yang, C., Liu, H., & Cao, Y. (2019) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2019.04.022 · Cited by 36 · see citing works
Kim, J. Y., Wang, L. Q., Sladky, V. C., Oh, T. G., Liu, J., Trinh, K., Eichin, F., Downes, M., Hosseini, M., Jacotot, E. D., et al. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2022.08.005 · Cited by 36 · see citing works
Self-citationPark, S., Helsley, R. N., Fadhul, T., Willoughby, J. L. S., Noetzli, L. J., Tu, H.-C., Solheim, M. H., Fujisaka, S., Pan, H., Dreyfuss, J. M., et al. (2023) · Metabolism · doi:10.1016/j.metabol.2023.155591 · Cited by 36 · see citing works
Pan, Y., Wang, Y., Tang, W., Sun, W., Ma, Y., Lin, S., Jing, J., Jiang, L., Shi, H., Song, Z., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-61473-6 · Cited by 35 · see citing works
Wang, Y.-L., Zhou, X., Li, D., & Ye, J. (2021) · Acta Pharmacologica Sinica · doi:10.1038/s41401-021-00629-0 · Cited by 34 · see citing works
Lactational delivery of Triclosan promotes non-alcoholic fatty liver disease in newborn mice
Weber, A. A., Yang, X., Mennillo, E., Ding, J., Watrous, J. D., Jain, M., Chen, S., Karin, M., & Tukey, R. H. (2022) · Nature Communications · doi:10.1038/s41467-022-31947-4 · Cited by 33 · see citing works
Self-citation
- Authors
- Kim, J. Y., Garcia-Carbonell, R., Yamachika, S., Zhao, P., Dhar, D., Loomba, R., Kaufman, R. J., Saltiel, A. R., & Karin, M.
- Affiliations
- University of California San Diego (US)
- Sanford Burnham Prebys Medical Discovery Institute (US)
- Corresponding author
- Karin, Michael
- ORCID
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2018-09
- Volume
- 175
- Issue
- 1
- Pages
- 133-145.e15
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC6159928
- OpenAlex
- W2890819762
- Cited by
- 333
- References
- 59
- Citations by year
- 2026: 16 · 2025: 45 · 2024: 48 · 2023: 49 · 2022: 49 · 2021: 49 · 2020: 49 · 2019: 24 · 2018: 4
- FWCI
- 24.60
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- NIH
- NCI (R01CA211794, R01CA198103, R01CA155120)
- NIEHS (P42ES010337)
- NHMRC (APP112227)
- AACR-Bayer Hepatocellular Carcinoma Fellowship (16-40-44-KIMJ)
- Diabetes Research Center Pilot and Feasibility Grant (P30DK063491)
- Boehringer Ingelheim Fonds
- Topics
- Health Sciences › Medicine › Epidemiology › Liver Disease Diagnosis and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Endoplasmic Reticulum Stress and Disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Lipids, and Metabolism
- Keywords
- endoplasmic reticulum stress, nonalcoholic steatohepatitis, non-alcoholic fatty liver disease, caspase-2, site-1 protease, de novo lipogenesis, hepatic steatosis, free cholesterol accumulation, triglyceride accumulation
- MeSH terms
- Animals, Cholesterol, Endoplasmic Reticulum, Fatty Liver, Humans, Liver, Mice, Inbred C57BL, Serine Endopeptidases, Triglycerides, Hepatocytes, Proprotein Convertases, Lipogenesis, Mice, Sterol Regulatory Element Binding Protein 1, Caspase 2, HEK293 Cells, Endoplasmic Reticulum Stress
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review