Electronic Journal of Liver Tumor ›› 2025, Vol. 12 ›› Issue (2): 22-25.
• Review • Previous Articles Next Articles
Zhao Weihua, Li Changying*
Received:
2024-06-12
Published:
2025-07-29
Contact:
*Li Changying, E-mail: changyingli1006@163.com
Zhao Weihua, Li Changying. Advances in study on farnesoid X receptor in hepatocellular carcinoma[J]. Electronic Journal of Liver Tumor, 2025, 12(2): 22-25.
[1] HOOFNAGLE J H.FXR agonists as therapy for liver disease[J]. Hepatology, 2020, 72(1): 1-3. [2] ZHOU J, CUI S, HE Q, et al.SUMOylation inhibitors synergize with FXR agonists in combating liver fibrosis[J]. Nat Commun, 2020, 11(1): 240. [3] DAWSON P A.Hepatic bile acid uptake in humans and mice: multiple pathways and expanding potential role for gut-liver signaling[J]. Hepatology, 2017, 66(5): 1384-1386. [4] CHIANG J Y L, Ferrell JM. Discovery of farnesoid X receptor and its role in bile acid metabolism[J]. Mol Cell Endocrinol, 2022, 548: 111618. [5] FAN M, WANG X, XU G, et al.Bile acid signaling and liver regeneration[J]. Biochim Biophys Acta, 2015, 1849(2): 196-200. [6] MASSAFRA V, VAN MIL S W C. Farnesoid X receptor: a "homeostat" for hepatic nutrient metabolism[J]. Biochim Biophys Acta Mol Basis Dis, 2018, 1864(1): 45-59. [7] ZHENG R S, CHEN R, HAN B F, et al.Cancer incidence and mortality in China, 2022[J]. J Natl Cancer Cent, 2024, 46(3) :221-231. [8] SUN L, CAI J, GONZALEZ F J.The role of farnesoid X receptor in metabolic diseases,and gastrointestinal and liver cancer[J]. Nat Rev Gastroenterol Hepatol, 2021, 18(5): 335-347. [9] LI T, APTE U.Bile acid metabolism and signaling in cholestasis,inflammation,and cancer[J]. Adv Pharmacol, 2015, 74: 263-302. [10] KIMHOFER T, FYE H, TAYLOR-ROBINSON S, et al.Proteomic and metabonomic biomarkers for hepatocellular carcinoma: a comprehensive review[J]. Br J Cancer, 2015, 112(7): 1141-1156. [11] TAKAHASHI S, TANAKA N, FUKAMI T, et al.Role of farnesoid X receptor and bile acids in hepatic tumor development[J]. Hepatol Commun, 2018, 2(12): 1567-1582. [12] ANAKK S, BHOSALE M, SCHMIDT V A, et al.Bile acids activate YAP to promote liver carcinogenesis[J]. Cell Rep, 2013, 5(4): 1060-1069. [13] YOSHIMOTO S, LOO T M, ATARASHI K, et al.Obesity-induced gut microbial metabolite promotes liver cancer through senescence secretome[J]. Nature, 2013, 499(7456): 97-101. [14] MA C, HAN MJ, HEINRICH B, et al.Gut microbiome-mediated bile acid metabolism regulates liver cancer via NKT cells[J]. Science, 2018, 360(6391): 1-23. [15] DEGIROLAMO C, MODICA S, VACCA M, et al.Prevention of spontaneous hepatocarcinogenesis in farnesoid X receptor-null mice by intestinal-specific farnesoid X receptor reactivation[J]. Hepatology, 2015, 61(1): 161-170. [16] KAINUMA M, TAKADA I, MAKISHIMA M, et al.Farnesoid X receptor activation enhances transforming growth factor β-induced epithelial-mesenchymal transition in hepatocellular carcinoma cells[J]. Int J Mol Sci, 2018, 19(7): 1898. [17] STOFAN M, GUO G L.Bile acids and FXR:novel targets for liver diseases[J]. Front Med(Lausanne), 2020, 7: 544. [18] FERRELL J M, PATHAK P, BOEHME S, et al.Deficiency of both farnesoid x receptor and takeda g protein-coupled receptor 5 exacerbated liver fibrosis in mice[J]. Hepatology, 2019, 70(3): 955-970. [19] HUANG X F, ZHAO W Y, HUANG W D.FXR and liver carcinogenesis[J]. Acta Pharmacol Sin, 2015, 36(1): 37-43. [20] LIU N, MENG Z, LOU G, et al.Hepatocarcinogenesis in FXR-/- mice mimics human HCC progression that operates through HNF1α regulation of FXR expression[J]. Mol Endocrinol, 2012, 26(5): 775-785. [21] MENG Z,WANG X, GAN Y, et al.Deletion of IFNγ enhances hepatocarcinogenesis in FXR knockout mice[J]. J Hepatol, 2012, 57(5): 1004-1012. [22] ZHANG Y, GE X, HEEMSTRA L A, et al.Loss of FXR protects against diet-induced obesity and accelerates liver carcinogenesis in Ob/Ob mice[J]. Mol Endocrinol, 2012, 26(2): 272-280. [23] CARIELLO M, PERES C, ZERLOTIN R, et al.Long-term administration of nuclear bile acid receptor FXR agonist prevents spontaneous hepatocarcinogenesis in Abcb4-/- mice[J]. Sci Rep, 2017, 7(1): 11203. [24] KONG B, ZHU Y, LI G, et al.Mice with hepatocyte-specific FXR deficiency are resistant to spontaneous but susceptible to cholic acid-induced hepatocarcinogenesis[J]. Am J Physiol Gastrointest Liver Physiol, 2016, 310(5): 295-302. [25] ZHANG C,WANG Z,FENG Q, et al.Farnesoid X receptor: a potential therapeutic target in multiple organs[J]. Histol Histopathol, 2020, 35(12): 1403-1414. [26] TAKAHASHI S, TANAKA N, GOLLA S, et al.Editor's highlight:Farnesoid X receptor protects against low-dose carbon tetrachloride-induced liver injury through the taurocholate-JNK pathway[J]. Toxicol Sci, 2017, 158(2): 334-346. [27] KONG B, WANG L, CHIANG J Y, et al.Mechanism of tissue-specific farnesoid X receptor in suppressing the expression of genes in bile-acid synthesis in mice[J]. Hepatology, 2012, 56(3): 1034-1043. [28] LI Q, ZHAO Q, ZHANG C Z, et al.The ileal FGF15/19 to hepatic FGFR4 axis regulates liver regeneration after partial hepatectomy in mice[J]. J Physiol Biochem, 2018, 74(2): 247-260. [29] RAJA A, PARK I, HAQ F, et al.FGF19-FGFR4 signaling in hepatocellular carcinoma[J]. Cells, 2019, 8(6): 536. [30] CHEN J, DU F, DANG Y, et al.Fibroblast growth factor 19-mediated up-regulation of SYR-related high-mobility group Box 18 promotes hepatocellular carcinoma metastasis by transactivating fibroblast growth factor receptor 4 and Fms-related tyrosine kinase 4[J]. Hepatology, 2020, 71(5): 1712-1731. [31] ZHOU M, LUO J, CHEN M, et al.Mouse species-specific control of hepatocarcinogenesis and metabolism by FGF19/FGF15[J]. J Hepatol, 2017, 66(6): 1182-1192. [32] JIA J, ZHOU X, CHU Q.Mechanisms and therapeutic prospect of the JAK-STAT signaling pathway in liver cancer[J]. Mol Cell Biochem, Epub 2024. [33] LEE K W, LIM S, KIM K D.The function of N-Myc downstream-regulated gene 2 (NDRG2) as a negative regulator in tumor cell metastasis[J]. Int J Mol Sci, 2022, 23(16): 9365. [34] HE J, ZHAO K, ZHENG L, et al.Upregulation of microRNA-122 by farnesoid X receptor suppresses the growth of hepatocellular carcinoma cells[J]. Mol Cancer, 2015, 14: 163. [35] KIM R D, SARKER D, MEYER T, et al.First-in-human phase I study of fisogatinib(BLU-554) validates aberrant FGF19 signaling as a driver event in hepatocellular carcinoma[J]. Cancer Discov, 2019, 9(12): 1696-1707. [36] LIU T, YANG H, FAN W, et al.Mechanisms of MAFG dysregulation in cholestatic liver injury and development of liver cancer[J]. Gastroenterology, 2018, 155(2): 557-571. [37] CARIELLO M, PERES C, ZERLOTINET R, et al.Long-term administration of nuclear bile acid receptor FXR agonist prevents spontaneous hepatocarcinogenesis in Abcb4-/- mice[J]. Sci Rep, 2017, 7(1): 11203. [38] GONG Y, LI K, QIN Y, et al.Norcholic acid promotes tumor progression and immune escape by regulating farnesoid X receptor in hepatocellular carcinoma[J]. Front Oncol, 2021, 11: 1-12. [39] FENG S, XIE X, CHEN C, et al.Alpha-linolenic acid inhibits hepatocellular carcinoma cell growth through farnesoid X receptor/β-catenin signaling pathway[J]. Nutr Metab (Lond), 2022,19(1): 57. [40] SHI J J, JIA X L, LI M, et al.Guggulsterone induces apoptosis of human hepatocellular carcinoma cells through intrinsic mitochondrial pathway[J]. World J Gastroenterol, 2015, 21(47): 13277-13287. [41] GIRISA S, PARAMA D, HARSHA C, et al.Potential of guggulsterone,a farnesoid X receptor antagonist,in the prevention and treatment of cancer[J]. Explor Target Antitumor Ther, 2020, 1(5): 313-342. |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||