An overview of resistance to Human epidermal growth factor receptor 2(Her2)targeted therapies in breast cancer
作者机构:Department of Pharmacology and ToxicologyFaculty of PharmacyKafrelsheikh UniversityKafrelsheikh 33516Egypt. Department of Pharmacology and ToxicologyVirginia Commonwealth UniversityRichmondVA 23298USA.
出 版 物:《Cancer Drug Resistance》 (癌症耐药(英文))
年 卷 期:2022年第5卷第2期
页 面:472-486页
学科分类:1002[医学-临床医学] 100214[医学-肿瘤学] 10[医学]
基 金:National Institutes of Health, NIH National Cancer Institute, NCI, (81XWH19-1-0490, CA260819) California Breast Cancer Research Program, CBCRP
主 题:HER2+ Targeted therapy resistance IGF-IR Src c-MET PP2A CD36 miRNA
摘 要:Breast cancer(BC)is the second most common cause of cancer-related deaths and the most frequently diagnosed cancer in *** 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 ***2+breast cancer is currently managed with multidisciplinary treatment strategies including surgery,radiation,chemotherapy,and targeted *** resistance remains a continuing challenge,especially to targeted therapy utilizing monoclonal antibodies and tyrosine kinase *** 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^(kip1),and miRNAs.