Inhibition of the Cyclin-Dependent Kinases (CDK) 4/6 as Therapy for Estrogen Receptor Positive Breast Cancer

A. Castrellon, S. Nguyen, L. Raez
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引用次数: 1

Abstract

Endocrine therapy (ET) is the usual first-line therapy for patients with hormone receptor-positive metastatic breast cancer (HR+MBC). However, resistance to ET frequently occurs during the course of treatment. Cellular pathways involved in cell proliferation are targets for new drugs that interfere with development of resistance to ET. Cyclin-dependent kinases (CDKs) are a subgroup of serine/ threonine kinases that play a key role in regulating cell cycle progression. In this review, we discuss the currently approved and under investigation CDK 4/6 inhibitors, in addition to their preclinical data and clinical trials that demonstrated their benefit in the treatment of HR+ breast cancer.
抑制细胞周期蛋白依赖性激酶(CDK) 4/6治疗雌激素受体阳性乳腺癌
内分泌治疗(ET)是激素受体阳性转移性乳腺癌(HR+MBC)患者常用的一线治疗方法。然而,在治疗过程中,对ET的耐药性经常发生。参与细胞增殖的细胞通路是干扰ET抗性发展的新药的靶标。细胞周期蛋白依赖性激酶(CDKs)是丝氨酸/苏氨酸激酶的一个亚组,在调节细胞周期进程中起关键作用。在这篇综述中,我们讨论了目前批准和正在研究的cdk4 /6抑制剂,以及它们的临床前数据和临床试验,这些数据和临床试验证明了它们在治疗HR+乳腺癌方面的益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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