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中国临床药理学与治疗学 ›› 2018, Vol. 23 ›› Issue (6): 715-720.doi: 10.12092/j.issn.1009-2501.2018.06.020

• 综述与讲座 • 上一篇    

他莫昔芬诱导非酒精性脂肪肝的机制研究进展

陈 曦1,凌嘉伟1,丁嘉欣1,江振洲1,3,张陆勇1,2   

  1. 1中国药科大学江苏省新药筛选重点实验室,南京 210009,江苏;2广东药科大学药学院新药筛选与药效学评价中心,广州 510006,广东;3药物质量与安全预警教育部重点实验室(中国药科大学),南京 210009,江苏
  • 收稿日期:2018-03-19 修回日期:2018-04-18 出版日期:2018-06-26 发布日期:2018-06-19
  • 通讯作者: 张陆勇,男,教授,博导,研究方向:分子药理学,高通量高内涵药物筛选。 Tel:02583271023 Email: lyzhang@cpu.edu.cn
  • 作者简介:陈曦,女,硕士研究生,研究方向:分子药理学。 Tel:18251982192 E-mail:chenxi199307@163.com
  • 基金资助:

    国家自然科学基金面上项目(81773827);公益性行业科研专项(201507004-002);国家重大新药创制专项(2015ZX09501004-002-004);国家自然科学基金重大国际(地区)合作研究项目(81320108029)

Advances in pathogenesis of nonalcoholic fatty liver disease caused by tamoxifen

CHEN Xi 1, LING Jiawei 1, DING Jiaxin 1, JIANG Zhenzhou 1,3, ZHANG Luyong 1,2   

  1. 1 Jiangsu Key Laboratory of Drug Screening, China Pharmaceutical University, Nanjing 210009, Jiangsu, China; 2 Center for Drug Screening and Pharmacodynamics Evaluation, School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, Guangdong, China; 3 Key Laboratory of Drug Quality Control and Pharmacovigilance (China Pharmaceutical University), Ministry of Education, Nanjing 210009, Jiangsu, China
  • Received:2018-03-19 Revised:2018-04-18 Online:2018-06-26 Published:2018-06-19

摘要:

选择性雌激素受体拮抗剂他莫昔芬目前在临床上乳腺癌术后内分泌治疗的应用中最为广泛,然而,越来越多的证据显示他莫昔芬可大大提高乳腺癌患者非酒精性脂肪肝的发病风险。目前关于他莫昔芬造成肝脏脂毒性的研究并不详尽,其造成非酒精性脂肪肝的具体机制仍不明确,本文对他莫昔芬诱导非酒精性脂肪肝这一现象及其机制研究进展进行综述,为后续深入探索其机制及研发治疗药物提供参考。

关键词: 他莫昔芬, 辅助内分泌治疗, 非酒精性脂肪肝, 发病机制

Abstract:

Tamoxifen, a selective estrogen receptor antagonist, is most widely used for endocrine therapy for breast cancer. However, mounting evidence suggests that tamoxifen treatment can significantly improve the risk of nonalcoholic fatty liver disease (NAFLD) in breast cancer patients. At present, there is no enough research on hepatic lipotoxicity caused by tamoxifen, the exact mechanism of it is still unknown. In this paper, we reviewed the phenomenon and mechanism of tamoxifen induced nonalcoholic fatty liver disease, providing references for further mechanism research and therapeutic drugs development.

Key words: tamoxifen, endocrine therapy, nonalcoholic fatty liver disease, pathogenesis

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