Lee W H, Chen P L, Riley D J
Center for Molecular Medicine/Institute of Biotechnology, University of Texas Health Science Center at San Antonio 78245, USA.
Ann N Y Acad Sci. 1995 Mar 27;752:432-45. doi: 10.1111/j.1749-6632.1995.tb17453.x.
Studies of the retinoblastoma (RB) gene product suggest that it may work as a fundamental regulator to coordinate pathways of cellular growth and differentiation. One known function of retinoblastoma (Rb) protein is its ability to suppress tumorigenesis. In many different cultured tumor cells, replacement of a normal RB gene and expression of normal Rb protein results in suppression of neoplastic properties. Moreover, in humans or experimental mice, germ line mutation of the RB gene leads particularly to retinoblastomas or pituitary tumors, respectively, which demonstrates that the role of RB in tumor predisposition is specific to certain tissues. In addition to suppressing tumor formation, Rb apparently also has roles in normal development and cellular differentiation. Recent characterizations of Rb-associated proteins and proteins within the Rb family may provide some clues to exploring the complex networks in which Rb is involved.
对视网膜母细胞瘤(RB)基因产物的研究表明,它可能作为一种基本调节因子来协调细胞生长和分化途径。视网膜母细胞瘤(Rb)蛋白的一个已知功能是其抑制肿瘤发生的能力。在许多不同的培养肿瘤细胞中,正常RB基因的替换和正常Rb蛋白的表达会导致肿瘤特性的抑制。此外,在人类或实验小鼠中,RB基因的种系突变分别特别导致视网膜母细胞瘤或垂体肿瘤,这表明RB在肿瘤易感性中的作用对某些组织具有特异性。除了抑制肿瘤形成外,Rb显然在正常发育和细胞分化中也发挥作用。最近对Rb相关蛋白和Rb家族内蛋白质的表征可能为探索Rb所涉及的复杂网络提供一些线索。