期刊文献+

CDK4/6抑制剂治疗三阴性乳腺癌的研究进展 被引量:3

Advances in the treatment of triple-negative breast cancer with CDK4/6 inhibitors
下载PDF
导出
摘要 细胞周期的调控机制在肿瘤的发生、发展中发挥着重要作用。多项研究表明,在雌激素受体阳性、人类表皮生长因子受体阴性的乳腺癌患者中,细胞周期蛋白依赖性激酶4/6(cyclin-dependent kinase 4/6,CDK4/6)抑制剂具有较好的疗效,然而其在三阴性乳腺癌患者中的疗效仍需进一步探讨。Cyclin D-CDK4/6-INK4-Rb-E2F信号通路因具有调控细胞周期检查点的作用,被认为是乳腺癌潜在的治疗靶点。寻找三阴性乳腺癌与CDK4/6抑制剂关联的生物标志物,探究合理的药物配伍,筛选能从中获益的靶向人群,对临床工作具有重要意义。对CDK4/6抑制剂在三阴性乳腺癌的研究进展进行综述,探讨其应用前景及优化手段。 The regulatory mechanism of cell cycle plays an important role in the occurrence and development of tumors.In recent years,a number of studies have shown that cyclin-dependent kinase 4/6(CDK4/6)inhibitors have good efficacy in patients with estrogen receptor-positive,human epidermal growth factor receptor-negative breast cancer,but their efficacy in patients with triple-negative breast cancer is still controversial.Cyclin D-CDK4/6-INK4-Rb-E2 F signaling pathway is considered as a potential therapeutic target for breast cancer due to its role in regulating cell cycle check points.It is of great significance to explore the molecular markers related to CDK4/6 inhibitors for triple-negative breast cancer,guide rational drug combination,and screen the population of triple-negative breast cancer patient who can benefit from this drug.In this article,we reviewed the research progress of CDK4/6 inhibitors in triple-negative breast cancer,and discussed their application prospects and optimization methods.
作者 朱秀之 陈力 纪磊 高雨 王中华 ZHU Xiuzhi;CHEN Li;JI Lei;GAO Yu;WANG Zhonghua(Department of Breast Surgery,Key Laboratory of Breast Cancer in Shanghai,Fudan University Shanghai Cancer Center,Department of Oncology,Shanghai Medical College,Fudan University,Shanghai 200032,China)
出处 《中国癌症杂志》 CAS CSCD 北大核心 2019年第11期899-905,共7页 China Oncology
基金 北京乳腺病防治学会乳腺癌预防与诊治科研基金(2016) 上海市抗癌协会青年医生“雏鹰”项目(2018)(SACA-CY1B02)
关键词 细胞周期蛋白依赖激酶4/6 细胞周期蛋白D和E 三阴性乳腺癌 视网膜母细胞瘤蛋白质 雄激素受体 Cyclin-dependent kinase 4/6 Cyclin D/E Triple-negative breast cancer Retinoblastoma protein Androgen receptor
  • 相关文献

参考文献1

共引文献5

同被引文献44

引证文献3

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部