Stiegler P, Kasten M, Giordano A
Department of Pathology, Anatomy and Cell Biology, Jefferson Medical College, Philadelphia, Pennsylvania 19107, USA.
J Cell Biochem Suppl. 1998;30-31:30-6.
The intense investigation of the retinoblastoma "tumor suppressor family" members, pRb, pRb2/p130, and p107, has revealed impressive mechanisms evolved to safeguard development and homeostasis in higher eukaryotes. Members of the retinoblastoma family are involved in implementing and controlling three major aspects of cellular life: (1) proliferative growth, (2) differentiation, and (3) apoptosis. The activities of these proteins are highly regulated, enabling them to precisely establish control. The pRb protein is well understood in its regulatory abilities and is considered a classical tumor suppressor. The role of pRb2/p130 protein in growth suppression and its potential as a tumor suppressor have been established during the last few years. The p107 protein, structurally and functionally similar to, but yet distinctive from, pRb2/p130, is characterized at a more rudimentary level. In this report, we review the latest data on the retinoblastoma protein family and its web of regulatory mechanisms.
对视网膜母细胞瘤“肿瘤抑制因子家族”成员pRb、pRb2/p130和p107的深入研究揭示了高等真核生物为保障发育和体内平衡而进化出的令人印象深刻的机制。视网膜母细胞瘤家族成员参与细胞生命的三个主要方面的实施和控制:(1)增殖性生长,(2)分化,以及(3)细胞凋亡。这些蛋白质的活性受到高度调控,使其能够精确地建立控制。pRb蛋白的调控能力已得到充分了解,被认为是一种经典的肿瘤抑制因子。在过去几年中,pRb2/p130蛋白在生长抑制中的作用及其作为肿瘤抑制因子的潜力已得到证实。p107蛋白在结构和功能上与pRb2/p130相似,但又有所不同,其特征仍处于更基础的层面。在本报告中,我们综述了关于视网膜母细胞瘤蛋白家族及其调控机制网络的最新数据。