视网膜母细胞瘤
视网膜母细胞瘤蛋白
生物
癌变
转录因子
染色质
染色质重塑
细胞生物学
细胞周期
细胞命运测定
细胞生长
细胞
转录调控
血管生成
癌症研究
基因
遗传学
作者
Paola Indovina,Eleonora Marcelli,Nadia Casini,Valeria Rizzo,Antonio Giordano
摘要
Abstract The retinoblastoma (RB) family of proteins, including RB1/p105, retinoblastoma‐like 1 (RBL1/p107), and retinoblastoma‐like 2 (RBL2/p130), is principally known for its central role on cell cycle regulation. The inactivation of RB proteins confers a growth advantage and underlies multiple types of tumors. Recently, it has been shown that RB proteins have other important roles, such as preservation of chromosomal stability, induction and maintenance of senescence and regulation of apoptosis, cellular differentiation, and angiogenesis. RB proteins are involved in many cellular pathways and act as transcriptional regulators able to bind several transcription factors, thus antagonizing or potentiating their functions. Furthermore, RB proteins might control the expression of specific target genes by recruiting chromatin remodeling enzymes. Although many efforts have been made to dissect the different functions of RB proteins, it remains still unclear which are necessary for cancer suppression and the role they play at distinct steps of carcinogenesis. Moreover, RB proteins can behave differently in various cell types or cell states. Elucidating the intricate RB protein network in regulating cell fate might provide the knowledge necessary to explain their potent tumor suppressor activity and to design novel therapeutic strategies. J. Cell. Physiol. 228: 525–535, 2013. © 2012 Wiley Periodicals, Inc.
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