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Effects of Estrogen and Estrogen Receptors on Transcriptomes of HepG2 Cells: A Preliminary Study Using RNA Sequencing.雌激素及雌激素受体对HepG2细胞转录组的影响:一项基于RNA测序的初步研究
Int J Endocrinol. 2018 Oct 28;2018:5789127. doi: 10.1155/2018/5789127. eCollection 2018.
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Obesity Drives STAT-1-Dependent NASH and STAT-3-Dependent HCC.肥胖驱动 STAT-1 依赖性 NASH 和 STAT-3 依赖性 HCC。
Cell. 2018 Nov 15;175(5):1289-1306.e20. doi: 10.1016/j.cell.2018.09.053. Epub 2018 Oct 25.
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MiR-133a acts as an anti-oncogene in Hepatocellular carcinoma by inhibiting FOSL2 through TGF-β/Smad3 signaling pathway.miR-133a 通过 TGF-β/Smad3 信号通路抑制 FOSL2 的表达,从而在肝癌中发挥抑癌基因的作用。
Biomed Pharmacother. 2018 Nov;107:168-176. doi: 10.1016/j.biopha.2018.07.151. Epub 2018 Aug 6.
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Serum miR-22 as potential non-invasive predictor of poor clinical outcome in newly diagnosed, uniformly treated patients with diffuse large B-cell lymphoma: an explorative pilot study.血清 miR-22 作为弥漫性大 B 细胞淋巴瘤新诊断且统一治疗患者不良临床结局的潜在非侵入性预测指标:一项探索性的初步研究。
J Exp Clin Cancer Res. 2018 May 2;37(1):95. doi: 10.1186/s13046-018-0768-5.
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Expression of sf1 and dax-1 are regulated by thyroid hormones and androgens during Silurana tropicalis early development.在热带爪蟾早期发育过程中,sf1和dax-1的表达受甲状腺激素和雄激素调控。
Gen Comp Endocrinol. 2018 Apr 1;259:34-44. doi: 10.1016/j.ygcen.2017.10.017. Epub 2017 Oct 28.
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Estrogen receptor expression in chronic hepatitis C and hepatocellular carcinoma pathogenesis.雌激素受体在慢性丙型肝炎和肝细胞癌发病机制中的表达。
World J Gastroenterol. 2017 Oct 7;23(37):6802-6816. doi: 10.3748/wjg.v23.i37.6802.
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Activation of SRY accounts for male-specific hepatocarcinogenesis: Implication in gender disparity of hepatocellular carcinoma.SRY 的激活导致男性特异性肝癌发生:对肝细胞癌性别差异的启示。
Cancer Lett. 2017 Dec 1;410:20-31. doi: 10.1016/j.canlet.2017.09.013. Epub 2017 Sep 21.
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Estrogen Replacement Reduces Risk and Increases Survival Times of Women With Hepatocellular Carcinoma.雌激素替代治疗降低了肝癌女性患者的发病风险并延长了其生存时间。
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Gender disparity in hepatocellular carcinoma (HCC): multiple underlying mechanisms.肝细胞癌(HCC)中的性别差异:多种潜在机制。
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NF90 regulates PARP1 mRNA stability in hepatocellular carcinoma.NF90调节肝癌中PARP1 mRNA的稳定性。
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肝细胞癌性别差异分子机制的最新进展

Recent advances in the molecular mechanism of sex disparity in hepatocellular carcinoma.

作者信息

Li Yanmeng, Xu Anjian, Jia Siyu, Huang Jian

机构信息

Experimental Center, Liver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, P.R. China.

National Clinical Research Center for Digestive Disease, Beijing 100050, P.R. China.

出版信息

Oncol Lett. 2019 May;17(5):4222-4228. doi: 10.3892/ol.2019.10127. Epub 2019 Mar 8.

DOI:10.3892/ol.2019.10127
PMID:30988804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6447942/
Abstract

Hepatocellular carcinoma (HCC) is more frequently observed and aggressive in men compared with women. Increasing evidence demonstrates that the sex disparity appears to be mediated by the stimulatory effects of androgens and the protective effects of estrogen in the development and progression of HCC. In the past few decades, studies on the sex difference of HCC mainly focused on the effect of sex hormones on the transactivation of hepatitis B virus X protein and the release of inflammatory cytokines, and these studies have further intensified in recent years. Sex hormones are also involved in genetic alterations and DNA damage repair in hepatocytes through binding to their specific cellular receptors and affecting the corresponding signaling pathways. Furthermore, the theory of sex chromosomes participating in HCC has been considered. The present review discussed the recent advances in the molecular mechanisms of sex disparity in HCC, with the aim of improving the understanding of the underlying critical factors and exploring more effective methods for the prevention and treatment of HCC.

摘要

与女性相比,肝细胞癌(HCC)在男性中更常见且侵袭性更强。越来越多的证据表明,这种性别差异似乎是由雄激素的刺激作用和雌激素在HCC发生发展中的保护作用介导的。在过去几十年中,关于HCC性别差异的研究主要集中在性激素对乙型肝炎病毒X蛋白反式激活和炎性细胞因子释放的影响上,并且这些研究近年来进一步加强。性激素还通过与其特定细胞受体结合并影响相应信号通路,参与肝细胞的基因改变和DNA损伤修复。此外,还考虑了性染色体参与HCC的理论。本综述讨论了HCC性别差异分子机制的最新进展,旨在增进对潜在关键因素的理解,并探索更有效的HCC预防和治疗方法。