Recent research progress on the role of BCL2 in cancer and related drugs

Bcl-2家族 转移 细胞凋亡 生物 癌症研究 调节器 癌症 癌细胞 小RNA 细胞 淋巴瘤 突变 蛋白质家族 程序性细胞死亡 基因 遗传学 免疫学
作者
Yubo Jianga,Yanbin Luan,Shuyan Wang,Baoyue Zhang
标识
DOI:10.1117/12.2669368
摘要

B-cell lymphoma (Bcl-2) proteins are a family of proteins that all have Bcl-2 homologous (BH) structural domains, such as Bcl-2, Bcl-xl, Bax, Bak and Bid. most Bcl-2 proteins have four BH structural domains (BH1, BH2, BH3 and BH4) which interact with each other. Although the bcl-2 family of proteins has long been recognized as a dominant regulator of apoptosis, beginning in the late 1990s, Sierra et al. found that bcl-2 not only limited the regulation of cell death, but also played an important role in cell migration, invasion, and tumor metastasis. In order to prove this idea, the literature on bcl- 2 family proteins was reviewed to understand the effects of bcl-2 family proteins on tumour invasion and metastasis and to investigate small molecule drugs for bcl-2 and microRNAs targeting bcl-2 inhibition. This article focuses on four main aspects of the bcl family, namely the bcl-2 composition, bcl mutation sites and their effect on tumour cell invasion and metastasis, the relationship between pro-apoptotic proteins and tumours and bcl-2 small molecule resistance. Expected to provide a theoretical basis for understanding drug studies of bcl inhibition of tumor metastasis.
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