The DOI matches its Crossref record; 23 of the 23 references it cites were found in a registry or an index.
A High-Cholesterol Diet Exacerbates Liver Fibrosis in Mice via Accumulation of Free Cholesterol in Hepatic Stellate Cells
Open accessAbstract
Background & aims Some studies have indicated that dietary cholesterol has a role in the progression of liver fibrosis. We investigated the mechanisms by which dietary cholesterol might contribute to hepatic fibrogenesis.Methods C57BL/6 mice were fed a high-cholesterol diet or a control diet for 4 weeks; liver fibrosis then was induced by bile-duct ligation or carbon tetrachloride administration. Hepatic stellate cells (HSCs) were isolated from mice fed high-cholesterol diets or from Niemann-Pick type C1-deficient mice, which accumulate intracellular free cholesterol.Results After bile-duct ligation or carbon tetrachloride administration, mice fed high-cholesterol diets had significant increases in liver fibrosis and activation of HSCs compared with mice fed control diets. There were no significant differences in the degree of hepatocellular injury or liver inflammation, including hepatocyte apoptosis or Kupffer cell activation, between mice fed high-cholesterol or control diets. Levels of free cholesterol were much higher in HSCs from mice fed high-cholesterol diets than those fed control diets. In cultured HSCs, accumulation of free cholesterol in HSCs increased levels of Toll-like receptor 4 (TLR4), leading to down-regulation of bone morphogenetic protein and activin membrane-bound inhibitor (a pseudoreceptor for transforming growth factor [TGF]β); the HSCs became sensitized to TGFβ-induced activation. Liver fibrosis was not aggravated by the high-cholesterol diet in C3H/HeJ mice, which express a mutant form of TLR4; HSCs that express mutant TLR4 were not activated by accumulation of free cholesterol.Conclusions Dietary cholesterol aggravates liver fibrosis because free cholesterol accumulates in HSCs, leading to increased TLR4 signaling, down-regulation of bone morphogenetic protein and activin membrane-bound inhibitor, and sensitization of HSC to TGFβ. This pathway might be targeted by antifibrotic therapies.
Overview
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
Verification
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?
In the citing paper
“Increased cholesterol in turn promotes MASH fibrosis through the TAZ/Indian hedgehog pathway described above (232-234).”
From Found in translation—Fibrosis in metabolic dysfunction–associated steatohepatitis (MASH) (2023) · cites this paper as [232]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Mechanisms of Hepatic Fibrogenesis
Friedman, S. L. (2008) · Gastroenterology · doi:10.1053/j.gastro.2008.03.003 · Cited by 2,687
TLR4 enhances TGF-β signaling and hepatic fibrosis
Seki, E., De Minicis, S., Österreicher, C. H., Kluwe, J., Osawa, Y., Brenner, D. A., & Schwabe, R. F. (2007) · Nature Medicine · doi:10.1038/nm1663 · Cited by 1,942
Free Fatty Acids Induce JNK-dependent Hepatocyte Lipoapoptosis
Malhi, H., Bronk, S. F., Werneburg, N. W., & Gores, G. J. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m510660200 · Cited by 724
Paik, Y.-H., Schwabe, R. F., Bataller, R., Russo, M. P., Jobin, C., & Brenner, D. A. (2003) · Hepatology · doi:10.1053/jhep.2003.50182 · Cited by 651
Mitochondrial free cholesterol loading sensitizes to TNF- and Fas-mediated steatohepatitis
Marí, 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 624
Wouters, K., van Gorp, P. J., Bieghs, V., Gijbels, M. J., Duimel, H., Lütjohann, D., Kerksiek, A., van Kruchten, R., Maeda, N., Staels, B., et al. (2008) · Hepatology · doi:10.1002/hep.22363 · Cited by 482
Tomita, K., Tamiya, G., Ando, S., Ohsumi, K., Chiyo, T., Mizutani, A., Kitamura, N., Toda, K., Kaneko, T., Horie, Y., et al. (2005) · Gut · doi:10.1136/gut.2005.071118 · Cited by 454
Self-citationLi, Y., Schwabe, R. F., DeVries-Seimon, T., Yao, P. M., Gerbod-Giannone, M.-C., Tall, A. R., Davis, R. J., Flavell, R., Brenner, D. A., & Tabas, I. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m501759200 · Cited by 421
Ekstedt, M., Franzén, L. E., Mathiesen, U. L., Holmqvist, M., Bodemar, G., & Kechagias, S. (2007) · Journal of Hepatology · doi:10.1016/j.jhep.2007.02.013 · Cited by 272
Liao, G., Yao, Y., Liu, J., Yu, Z., Cheung, S., Xie, A., Liang, X., & Bi, X. (2007) · The American Journal of Pathology · doi:10.2353/ajpath.2007.070052 · Cited by 220
Research works printed but not linked: 2
- Paik, 2003, Toll-like receptor 4 mediates inflammatory signaling by bacterial lipopolysaccharide in human hepatic stellate cells, Hepatology, 37, 1043, 10.1053/jhep.2003.50182 · DOI · Paper page
- Seki, 2007, TLR4 enhances TGF-beta signaling and hepatic fibrosis, Nat Med, 13, 1324, 10.1038/nm1663 · DOI · Paper page
Cited by
Sorted by citations
Mechanisms of hepatic stellate cell activation
Tsuchida, T., & Friedman, S. L. (2017) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2017.38 · Cited by 2,909
Liver Fibrosis: Mechanistic Concepts and Therapeutic Perspectives
Roehlen, N., Crouchet, E., & Baumert, T. F. (2020) · Cells · doi:10.3390/cells9040875 · Cited by 1,237
Immunology in the liver — from homeostasis to disease
Heymann, F., & Tacke, F. (2016) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2015.200 · Cited by 1,180
Liver fibrosis: Pathophysiology, pathogenetic targets and clinical issues
Parola, M., & Pinzani, M. (2018) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2018.09.002 · Cited by 1,217
Lipotoxicity and the gut-liver axis in NASH pathogenesis
Marra, F., & Svegliati-Baroni, G. (2018) · Journal of Hepatology · doi:10.1016/j.jhep.2017.11.014 · Cited by 847
Mechanisms 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
Nonalcoholic Fatty Liver Disease: Pathogenesis and Disease Spectrum
Hardy, T., Oakley, F., Anstee, Q. M., & Day, C. P. (2016) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathol-012615-044224 · Cited by 641
The Role of Cholesterol in the Pathogenesis of NASH
Ioannou, G. N. (2016) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2015.11.008 · Cited by 498
Metabolic reprogramming in liver fibrosis
Horn, P., & Tacke, F. (2024) · Cell Metabolism · doi:10.1016/j.cmet.2024.05.003 · Cited by 432
The Power of Plasticity—Metabolic Regulation of Hepatic Stellate Cells
Trivedi, P., Wang, S., & Friedman, S. L. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2020.10.026 · Cited by 427
Hepatocyte TAZ/WWTR1 Promotes Inflammation and Fibrosis in Nonalcoholic Steatohepatitis
Wang, X., Zheng, Z., Caviglia, J. M., Corey, K. E., Herfel, T. M., Cai, B., Masia, R., Chung, R. T., Lefkowitch, J. H., Schwabe, R. F., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.09.016 · Cited by 413
Cholesterol metabolism and the pathogenesis of non-alcoholic steatohepatitis
Musso, G., Gambino, R., & Cassader, M. (2012) · Progress in Lipid Research · doi:10.1016/j.plipres.2012.11.002 · Cited by 415
Biomarkers of NAFLD progression: a lipidomics approach to an epidemic
Gorden, D. L., Myers, D. S., Ivanova, P. T., Fahy, E., Maurya, M. R., Gupta, S., Min, J., Spann, N. J., McDonald, J. G., Kelly, S. L., et al. (2015) · Journal of Lipid Research · doi:10.1194/jlr.p056002 · Cited by 372
Tomita, K., Teratani, T., Suzuki, T., Shimizu, M., Sato, H., Narimatsu, K., Okada, Y., Kurihara, C., Irie, R., Yokoyama, H., et al. (2014) · Hepatology · doi:10.1002/hep.26604 · Cited by 315
Self-citationRecent insights on the role of cholesterol in non-alcoholic fatty liver disease
Argüello, G., Balboa, E., Arrese, M. A., & Zanlungo, S. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2015.05.015 · Cited by 320
Non-alcoholic steatohepatitis: pathogenesis and novel therapeutic approaches
Schuppan, D., & Schattenberg, J. M. (2013) · Journal of Gastroenterology and Hepatology · doi:10.1111/jgh.12212 · Cited by 256
Lipidomic biomarkers and mechanisms of lipotoxicity in non-alcoholic fatty liver disease
Svegliati‐Baroni, G., Pierantonelli, I., Torquato, P., Marinelli, R., Ferreri, C., Chatgilialoglu, C., Bartolini, D., & Galli, F. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.05.029 · Cited by 255
Hepatic cholesterol transport and its role in non-alcoholic fatty liver disease and atherosclerosis
Li, H., Yu, X.-H., Ou, X., Ouyang, X.-P., & Tang, C. (2021) · Progress in Lipid Research · doi:10.1016/j.plipres.2021.101109 · Cited by 237
Metabolic Hallmarks of Hepatic Stellate Cells in Liver Fibrosis
Khomich, O. A., Ivanov, A. V., & Bartosch, B. (2019) · Cells · doi:10.3390/cells9010024 · Cited by 239
Role of Cholesterol‐Associated Steatohepatitis in the Development of NASH
Horn, C. L., Morales, A. L., Savard, C. E., Farrell, G. C., & Ioannou, G. N. (2021) · Hepatology Communications · doi:10.1002/hep4.1801 · Cited by 224
Cholesterol 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
Mitochondrial cholesterol: Metabolism and impact on redox biology and disease
Goicoechea, L., de la Rosa, L. C., Torres, S., García‐Ruiz, C., & Fernández-Checa, J. C. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102643 · Cited by 196
Pathophysiological mechanisms underlying MAFLD
Kuchay, M. S., Choudhary, N. S., & Mishra, S. K. (2020) · Diabetes & Metabolic Syndrome Clinical Research & Reviews · doi:10.1016/j.dsx.2020.09.026 · Cited by 188
Toll-Like Receptors in Liver Fibrosis: Cellular Crosstalk and Mechanisms
Yang, L., & Seki, E. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00138 · Cited by 184
Found in translation—Fibrosis in metabolic dysfunction–associated steatohepatitis (MASH)
Wang, S., & Friedman, S. L. (2023) · Science Translational Medicine · doi:10.1126/scitranslmed.adi0759 · Cited by 158
Metabolic liver disease in diabetes – From mechanisms to clinical trials
Dewidar, B., KAHL, S., Pafili, K., & Roden, M. (2020) · Metabolism · doi:10.1016/j.metabol.2020.154299 · Cited by 167
Noureddin, M., Zelber‐Sagi, S., Wilkens, L. R., Porcel, J., Boushey, C. J., Le Marchand, L., Rosen, H. R., & Setiawan, V. W. (2020) · Hepatology · doi:10.1002/hep.30967 · Cited by 148
Takeshita, Y., Takamura, T., Honda, M., Kita, Y., Zen, Y., Kato, K., Misu, H., Ota, T., Nakamura, M., Yamada, K., et al. (2014) · Diabetologia · doi:10.1007/s00125-013-3149-9 · Cited by 137
Jiang, Y., Xiang, C., Zhong, F., Zhang, Y., Wang, L., Zhao, Y., Wang, J., Ding, C., Li, J., He, F., et al. (2020) · Theranostics · doi:10.7150/thno.46360 · Cited by 124
Liu, H., Pathak, P., Boehme, S., & Chiang, J. Y. L. (2016) · Journal of Lipid Research · doi:10.1194/jlr.m069807 · Cited by 125
MASH: the nexus of metabolism, inflammation, and fibrosis
Steinberg, G. R., Carpentier, A. C., & Wang, D. (2025) · Journal of Clinical Investigation · doi:10.1172/jci186420 · Cited by 135
Role of Metabolism in Hepatic Stellate Cell Activation and Fibrogenesis
Hou, W., & Syn, W. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00150 · Cited by 121
Liu, M., Xu, Y., Han, X., Yin, L., Xu, L., Qi, Y., Zhao, Y., Liu, K., & Peng, J. (2015) · Scientific Reports · doi:10.1038/srep18038 · Cited by 120
Hatle, K. M., Gummadidala, P. M., Navasa, N., Bernardo, E., Dodge, J. T., Silverstrim, B., Fortner, K. A., Burg, E., Suratt, B. T., Hammer, J., et al. (2013) · Molecular and Cellular Biology · doi:10.1128/mcb.00189-13 · Cited by 117
Zisser, A., Ipsen, D. H., & Tveden‐Nyborg, P. (2021) · Biomedicines · doi:10.3390/biomedicines9040365 · Cited by 112
Targeted Drug Delivery to Hepatic Stellate Cells for the Treatment of Liver Fibrosis
Chen, Z., Jain, A., Liu, H., Zhao, Z., & Cheng, K. (2019) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.118.256156 · Cited by 105
Stellate Cells in Tissue Repair, Inflammation, and Cancer
Sherman, M. H. (2018) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100617-062855 · Cited by 104
Nlrp3 is a key modulator of diet-induced nephropathy and renal cholesterol accumulation
Bakker, P. J., Butter, L. M., Kors, L., Teske, G. J. D., Aten, J., Sutterwala, F. S., Florquin, S., & Leemans, J. C. (2013) · Kidney International · doi:10.1038/ki.2013.503 · Cited by 98
Tomita, K., Teratani, T., Suzuki, T., Shimizu, M., Sato, H., Narimatsu, K., Usui∥, S., Furuhashi, H., Kimura, A., Nishiyama, K., et al. (2014) · Journal of Hepatology · doi:10.1016/j.jhep.2014.03.018 · Cited by 96
Self-citationPathophysiological underpinnings of metabolic dysfunction-associated steatotic liver disease
Kuchay, M. S., Choudhary, N. S., & Ramos‐Molina, B. (2025) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00951.2024 · Cited by 104
Ichimura‐Shimizu, M., Kawase, M., Masuzumi, M., Sakaki, M., Nagata, Y., Tanaka, K., Suruga, K., Tamaru, S., Kato, S., Tsuneyama, K., et al. (2014) · Hepatology Research · doi:10.1111/hepr.12358 · Cited by 88
Jump, D. Β., Depner, C. M., Tripathy, S., & Lytle, K. A. (2015) · Advances in Nutrition · doi:10.3945/an.115.009423 · Cited by 84
The role of iNOS in cholesterol-induced liver fibrosis
Anavi, S., Eisenberg‐Bord, M., Hahn-Obercyger, M., Genin, O., Pines, M., & Tirosh, O. (2015) · Laboratory Investigation · doi:10.1038/labinvest.2015.67 · Cited by 80
Hepatic Stellate Cells: Dictating Outcome in Nonalcoholic Fatty Liver Disease
Wiering, L., Subramanian, P., & Hammerich, L. (2023) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2023.02.010 · Cited by 80
Hypoxic Signaling and Cholesterol Lipotoxicity in Fatty Liver Disease Progression
Tirosh, O. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/2548154 · Cited by 77
Rossi, R. E., Conte, D., & Massironi, S. (2015) · Digestive and Liver Disease · doi:10.1016/j.dld.2015.05.021 · Cited by 77
Targeting cell-intrinsic metabolism for antifibrotic therapy
Gilgenkrantz, H., Mallat, A., Moreau, R., & Lotersztajn, S. (2021) · Journal of Hepatology · doi:10.1016/j.jhep.2021.02.012 · Cited by 76
Nutrition in Alcoholic Liver Disease
Singal, A. K., & Charlton, M. (2012) · Clinics in Liver Disease · doi:10.1016/j.cld.2012.08.009 · Cited by 76
BMP Signalling at the Crossroad of Liver Fibrosis and Regeneration
Herrera, B. M., Addante, A., & Sánchez, A. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms19010039 · Cited by 79
Yang, X., Chen, J., Wang, J., Ma, S., Feng, W., Wu, Z., Guo, Y., Zhou, H., Mi, W., Chen, W., et al. (2022) · Immunity · doi:10.1016/j.immuni.2022.06.001 · Cited by 70
Liver X Receptors Regulate Cholesterol Metabolism and Immunity in Hepatic Nonparenchymal Cells
Endo‐Umeda, K., & Makishima, M. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20205045 · Cited by 68
Chan, Y.-T., Wang, N., Tan, H. Y., Li, S., & Feng, Y. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00548 · Cited by 63
Uil, M., Scantlebery, A. M. L., Butter, L. M., Larsen, P. W. B., de Boer, O. J., Leemans, J. C., Florquin, S., & Roelofs, J. J. T. H. (2018) · Scientific Reports · doi:10.1038/s41598-018-23839-9 · Cited by 61
Morrison, M. C., Liang, W., Mulder, P., Verschuren, L., Pieterman, E. J., Toet, K. H., Heeringa, P., Wielinga, P. Y., Kooistra, T., & Kleemann, R. (2014) · Journal of Hepatology · doi:10.1016/j.jhep.2014.12.011 · Cited by 61
Fibrotic Events in the Progression of Cholestatic Liver Disease
Wu, H., Chen, C., Ziani, S., Nelson, L. J., Avila, M. A., Nevzorova, Y. A., & Cubero, F. J. (2021) · Cells · doi:10.3390/cells10051107 · Cited by 62
The Space of Disse: The Liver Hub in Health and Disease
Sanz-García, C., Fernández-Iglesias, A., Gracia-Sancho, J., Arráez-Aybar, L. A., Nevzorova, Y. A., & Cubero, F. J. (2021) · Livers · doi:10.3390/livers1010002 · Cited by 57
Non‐alcoholic fatty liver disease
Tuyama, A. C., & Chang, C. (2012) · Journal of Diabetes · doi:10.1111/j.1753-0407.2012.00204.x · Cited by 58
Teratani, T., Tomita, K., Furuhashi, H., Sugihara, N., Higashiyama, M., Nishikawa, M., Irie, R., Takajo, T., Wada, A., Horiuchi, K., et al. (2019) · Hepatology Communications · doi:10.1002/hep4.1383 · Cited by 56
Self-citationCholesterol and nonalcoholic fatty liver disease: Renewed focus on an old villain
Kerr, T. A., Davidson, N. O., Groszmann, R. J., Iwakiri, Y., & Taddei, T. H. (2012) · Hepatology · doi:10.1002/hep.26088 · Cited by 55
Diabetes as a risk factor for MASH progression
Gancheva, S., Roden, M., & Castéra, L. (2024) · Diabetes Research and Clinical Practice · doi:10.1016/j.diabres.2024.111846 · Cited by 60
Miura, K., Ohnishi, H., Morimoto, N., Minami, S., Ishioka, M., Watanabe, S., Tsukui, M., Takaoka, Y., Nomoto, H., Isoda, N., et al. (2018) · Cancer Science · doi:10.1111/cas.13902 · Cited by 54
Lysosomal cholesterol overload in macrophages promotes liver fibrosis in a mouse model of NASH
Itoh, M., Tamura, A., KANAI, S., Tanaka, M., Kanamori, Y., Shirakawa, I., Ito, A., Oka, Y., Hidaka, I., Takami, T., et al. (2023) · The Journal of Experimental Medicine · doi:10.1084/jem.20220681 · Cited by 52
Kitsugi, K., Noritake, H., Matsumoto, M., Hanaoka, T., Umemura, M., Yamashita, M., Takatori, S., Ito, J., Ohta, K., Chida, T., et al. (2023) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2023.166750 · Cited by 53
Okazaki, I., Noro, T., Tsutsui, N., Yamanouchi, E., Kuroda, H., Nakano, M., Yokomori, H., & Inagaki, Y. (2014) · Cancers · doi:10.3390/cancers6031220 · Cited by 55
Review article: emerging anti‐fibrotic therapies in the treatment of non‐alcoholic steatohepatitis
Noureddin, M., Anstee, Q. M., & Loomba, R. S. (2016) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.13620 · Cited by 50
Du, W., & Wang, L. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.936196 · Cited by 53
Non-alcoholic fatty liver disease: What has changed in the treatment since the beginning?
Baran, B. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i39.14219 · Cited by 51
Dietary oleic acid regulates hepatic lipogenesis through a liver X receptor-dependent signaling
Ducheix, S., Montagner, A., Polizzi, A., Lasserre, F., Régnier, M., Marmugi, A., Benhamed, F., Bertrand‐Michel, J., Mselli-Lakhal, L., Loiseau, N., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0181393 · Cited by 53
Chitinase 3‐like 1 deficiency ameliorates liver fibrosis by promoting hepatic macrophage apoptosis
Higashiyama, M., Tomita, K., Sugihara, N., Nakashima, H., Furuhashi, H., Nishikawa, M., Inaba, K., Wada, A., Horiuchi, K., Hanawa, Y., et al. (2019) · Hepatology Research · doi:10.1111/hepr.13396 · Cited by 50
Self-citationThelwall, P. E., Smith, F. E., Leavitt, M. C., Canty, D. J., Hu, W., Hollingsworth, K. G., Thoma, C., Trenell, M. I., Taylor, R., Rutkowski, J. V., et al. (2013) · Journal of Hepatology · doi:10.1016/j.jhep.2013.04.016 · Cited by 45
Nascè, A., Gariani, K., Jornayvaz, F. R., & Szántó, I. (2022) · Antioxidants · doi:10.3390/antiox11061131 · Cited by 49
Huang, P., Kaluba, B., Jiang, X.-L., Chang, S., Tang, X.-F., Mao, L.-F., Zhang, Z.-P., & Huang, F.-Z. (2018) · BioMed Research International · doi:10.1155/2018/8071093 · Cited by 44
Targeting fatty acid metabolism for fibrotic disorders
Hwang, S., & Chung, K. W. (2021) · Archives of Pharmacal Research · doi:10.1007/s12272-021-01352-4 · Cited by 47
Kotlyarov, S. N., & Bulgakov, A. (2021) · Cells · doi:10.3390/cells10112978 · Cited by 45
Lee, C.-Y., Suk, F., Twu, Y., & Liao, Y. (2020) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph17113802 · Cited by 43
Shaaban, H. H., AlZaim, I., El‐Mallah, A., Aly, R. G. M., EL‐Yazbi, A. F., & Wahid, A. M. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.120956 · Cited by 42
Gut microbiota combined with metabolomics reveal the mechanism of curcumol on liver fibrosis in mice
Zheng, Y., Wang, J., Wang, J., 姜瑞祝, Liang, T., & Zhao, T. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113204 · Cited by 41
Kanno, K., Koseki, M., Chang, J., Saga, A., Inui, H., Okada, T., Tanaka, K., Asaji, M., Zhu, Y., Ide, S., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-06542-8 · Cited by 44
Chen, P., Huang, C., Meng, X., & Li, J. (2015) · Biochimie · doi:10.1016/j.biochi.2015.06.016 · Cited by 41
Molenaar, M. R., Haaker, M. W., Vaandrager, A. B., Houweling, M., & Helms, J. B. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.103042 · Cited by 41
Kaminsky-Kolesnikov, Y., Rauchbach, E., Abu-Halaka, D., Hahn, M., García-Ruiz, C., Fernandez-Checa, J. C., Madar, Z., & Tirosh, O. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/5393761 · Cited by 39
Bruschi, F. V., Claudel, T., Tardelli, M., Starlinger, P., Marra, F., & Trauner, M. (2019) · Hepatology Communications · doi:10.1002/hep4.1395 · Cited by 38
Gerges, S. H., Wahdan, S. A., Elsherbiny, D. A., & El‐Demerdash, E. (2020) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2020.115101 · Cited by 39
Chen, L., Xia, H. H., Xin, Y., Lin, Z., & Xuan, S. (2015) · Journal of Clinical and Translational Hepatology · doi:10.14218/jcth.2015.00023 · Cited by 38
Zhang, H., Léveillé, M., Courty, É., Güneş, A., Nguyen, B., & Estall, J. L. (2020) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00321.2020 · Cited by 35
Traussnigg, S., Kienbacher, C., Halilbasic, E., Rechling, C., Kazemi-Shirazi, L., Hofer, H., Munda, P., & Trauner, M. A. (2015) · Digestive Diseases · doi:10.1159/000375353 · Cited by 37
Rauchbach, E., Zeigerman, H., Abu-Halaka, D., & Tirosh, O. (2022) · Antioxidants · doi:10.3390/antiox11030536 · Cited by 36
Impact of dietary fat on the development of non-alcoholic fatty liver disease in Ldlr−/− mice
Jump, D. Β., Depner, C. M., Tripathy, S., & Lytle, K. A. (2015) · Proceedings of The Nutrition Society · doi:10.1017/s002966511500244x · Cited by 36
Teratani, T., Tomita, K., Suzuki, T., Furuhashi, H., Irie, R., Hida, S., Okada, Y., Kurihara, C., Ebinuma, H., Nakamoto, N., et al. (2017) · Journal of Hepatology · doi:10.1016/j.jhep.2017.05.020 · Cited by 38
Self-citationUnderstanding and Treating Niemann–Pick Type C Disease: Models Matter
Pallottini, V., & Pfrieger, F. W. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21238979 · Cited by 40
Furuhashi, H., Tomita, K., Teratani, T., Shimizu, M., Nishikawa, M., Higashiyama, M., Takajo, T., Shirakabe, K., Maruta, K., Okada, Y., et al. (2017) · Hepatology Research · doi:10.1111/hepr.13040 · Cited by 34
Self-citationPillai, S. S., Lakhani, H. V., Zehra, M., Wang, J., Dilip, A., Puri, N., O'Hanlon, K. M., & Sodhi, K. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21186698 · Cited by 34
Huang, P. F., Tu, B., Liao, H.-J., Huang, F., Li, Z., Zhu, K.-Y., Dai, F., Liu, H.-Z., Zhang, T.-Y., & Sun, C. (2021) · Scientific Reports · doi:10.1038/s41598-021-85421-0 · Cited by 34
When GLP-1 hits the liver: a novel approach for insulin resistance and NASH
Kim, Y. O., & Schuppan, D. (2012) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00078.2012 · Cited by 34
Lipids in Liver Disease: Looking Beyond Steatosis
Schwabe, R. F., & Maher, J. J. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.11.004 · Cited by 33
Targeting Liver X Receptors for the Treatment of Non-Alcoholic Fatty Liver Disease
Kim, H.-J., Park, C., & Kim, T. H. (2023) · Cells · doi:10.3390/cells12091292 · Cited by 34
Cell metabolism-based therapy for liver fibrosis, repair, and hepatocellular carcinoma
Gilgenkrantz, H., Paradis, V., & Lotersztajn, S. (2023) · Hepatology · doi:10.1097/hep.0000000000000479 · Cited by 31
Dietary macro and micronutrients associated with MASLD: Analysis of a national US cohort database
Nemer, M., Osman, F., & Said, A. (2024) · Annals of Hepatology · doi:10.1016/j.aohep.2024.101491 · Cited by 36
Immunoregulation by lipids during the development of non-alcoholic steatohepatitis.
Ramadori, P., Kroy, D. C., & Streetz, K. L. (2015) · Europe PMC (PubMed Central) · doi:10.3978/j.issn.2304-3881.2015.01.02 · Cited by 31
From Liver Fat to Cancer: Perils of the Western Diet
Kim, J. Y., He, F., & Karin, M. (2021) · Cancers · doi:10.3390/cancers13051095 · Cited by 32
Metadata
- Authors
- Teratani, T., Tomita, K., Suzuki, T., Oshikawa, T., Yokoyama, H., Shimamura, K., Tominaga, S., Hiroi, S., Irie, R., Okada, Y., Kurihara, C., Ebinuma, H., Saito, H., Hokari, R., Sugiyama, K., Kanai, T., Miura, S., & Hibi, T.
- Affiliations
- Keio University (JP)
- National Defense Medical College (JP)
- Kawasaki Municipal Hospital (JP)
- Corresponding author
- Tomita, Kengo
- ORCID
- Venue
- Gastroenterology
- Publisher
- Elsevier BV
- Published
- 2012-01
- Volume
- 142
- Issue
- 1
- Pages
- 152-164.e10
- ISSN
- 0016-5085 (ISSN-L)
- OpenAlex
- W1996266503
- Cited by
- 241
- References
- 23
- Citations by year
- 2026: 15 · 2025: 21 · 2024: 22 · 2023: 25 · 2022: 22 · 2021: 15 · 2020: 20 · 2019: 14 · 2018: 13 · 2017: 8 · 2016: 19 · 2015: 16 · 2014: 7 · 2013: 14 · 2012: 9
- FWCI
- 6.22
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Gastroenterology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ministry of Education, Culture, Sports, Science and Technology
- Topics
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Health Sciences › Medicine › Hepatology › Liver Disease Diagnosis and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Cholesterol and Lipid Metabolism
- Keywords
- dietary cholesterol, liver fibrosis, hepatic stellate cells, free cholesterol accumulation, TLR4, TGF-beta signaling, Niemann-Pick C1, bile duct ligation, carbon tetrachloride, hepatic fibrogenesis, antifibrotic therapy
- MeSH terms
- Niemann-Pick C1 Protein, Animals, Bile Ducts, Carbon Tetrachloride, Cholesterol, Dietary, Disease Models, Animal, Kupffer Cells, Ligation, Liver Cirrhosis, Male, Membrane Proteins, Mice, Inbred C3H, Mice, Inbred C57BL, Proteins, Time Factors, Signal Transduction, Transforming Growth Factor beta, Apoptosis, Mice, Knockout, Disease Progression, Intracellular Signaling Peptides and Proteins, Toll-Like Receptor 4, Mice, Niemann-Pick Disease, Type C, Hepatic Stellate Cells
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