Tecalco-Cruz Angeles C, Zepeda-Cervantes Jesús, Ramírez-Jarquín Josué O, Rojas-Ochoa Alberto
Programa en Ciencias Genómicas, Universidad Autónoma de la Ciudad de México (UACM), CDMX, Mexico City 03100, Mexico.
Departamento de Microbiología e Inmunología, Facultad de Medicina Veterinaria y Zootecnia, Universidad Nacional Autónoma de México (UNAM), CDMX, Mexico City 04510, Mexico.
Explor Target Antitumor Ther. 2021;2(6):496-510. doi: 10.37349/etat.2021.00060. Epub 2021 Dec 31.
Breast cancer (BC) is a highly heterogeneous neoplasm of the mammary tissue, causing the deaths of a large number of women worldwide. Nearly 70% and 20% of BC cases are estrogen receptor alpha positive (ERα+) and human epidermal growth factor receptor 2-positive (HER2+), respectively; therefore, ER and HER2 targeted therapies have been employed in BC treatment. However, resistance to these therapies has been reported, indicating a need for developing novel therapeutic strategies. Proteolysis-targeting chimeras (PROTACs) are new, promising therapeutic tools designed with a bimodular structure: one module allows specific binding to target proteins, and the other module allows efficient degradation of these target proteins. In this paper, PROTACs and their potential in controlling the progression of ERα and HER2+ BC are discussed.
乳腺癌(BC)是一种乳腺组织高度异质性的肿瘤,在全球导致大量女性死亡。近70%和20%的乳腺癌病例分别为雌激素受体α阳性(ERα+)和人表皮生长因子受体2阳性(HER2+);因此,ER和HER2靶向治疗已应用于乳腺癌治疗。然而,已有报道称对这些治疗存在耐药性,这表明需要开发新的治疗策略。蛋白酶靶向嵌合体(PROTACs)是一种新型的、有前景的治疗工具,其设计具有双模块结构:一个模块允许与靶蛋白特异性结合,另一个模块允许有效降解这些靶蛋白。本文讨论了PROTACs及其在控制ERα和HER2+乳腺癌进展方面的潜力。