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乳腺癌中对人表皮生长因子受体2(Her2)靶向治疗的耐药性概述。

An overview of resistance to Human epidermal growth factor receptor 2 (Her2) targeted therapies in breast cancer.

作者信息

Elshazly Ahmed M, Gewirtz David A

机构信息

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Kafrelsheikh University, Kafrelsheikh 33516, Egypt.

Department of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond, VA 23298, USA.

出版信息

Cancer Drug Resist. 2022 Jun 1;5(2):472-486. doi: 10.20517/cdr.2022.09. eCollection 2022.

Abstract

Breast cancer (BC) is the second most common cause of cancer-related deaths and the most frequently diagnosed cancer in females. Among breast cancer types, HER2-positive breast cancer occurs in nearly 20% of human breast cancers and is associated with increased aggressiveness, poor prognosis, and shortened overall survival. HER2+ breast cancer is currently managed with multidisciplinary treatment strategies including surgery, radiation, chemotherapy, and targeted therapy. Drug resistance remains a continuing challenge, especially to targeted therapy utilizing monoclonal antibodies and tyrosine kinase inhibitors. This review discusses some of the recent molecular mechanisms that are involved in the development of resistance to Her2-targeted therapies including the PI3K/Akt/mTOR pathway, IGF-IR, Src, c-MET, the PP2A family, CD36, p27 and miRNAs.

摘要

乳腺癌(BC)是癌症相关死亡的第二大常见原因,也是女性中最常被诊断出的癌症。在乳腺癌类型中,HER2阳性乳腺癌占人类乳腺癌的近20%,并且与侵袭性增加、预后不良和总生存期缩短有关。目前,HER2 +乳腺癌采用包括手术、放疗、化疗和靶向治疗在内的多学科治疗策略进行管理。耐药性仍然是一个持续存在的挑战,尤其是对于使用单克隆抗体和酪氨酸激酶抑制剂的靶向治疗。本综述讨论了一些最近涉及对Her2靶向治疗耐药性发展的分子机制,包括PI3K/Akt/mTOR途径、IGF-IR、Src、c-MET、PP2A家族、CD36、p27和微小RNA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f101/9255238/8ea4641c115d/cdr-5-2-472.fig.1.jpg

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