Author: Sherr, C. J.
Description: Uncontrolled cell proliferation is the hallmark of cancer, and tumor cells have typically acquired damage to genes that directly regulate their cell cycles. Genetic alterations affecting p16(INK4a) and cyclin D1, proteins that govern phosphorylation of the retinoblastoma protein (RB) and control exit from the G1 phase of the cell cycle, are so frequent in human cancers that inactivation of this pathway may well be necessary for tumor development. Like the tumor suppressor protein p53, components of this “RB pathway,” although not essential for the cell cycle per se, may participate in checkpoint functions that regulate homeostatic tissue renewal throughout life.
Subject headings: Animals; Carrier Proteins; Cell Cycle; Cyclin-Dependent Kinase Inhibitor p16; Cyclin-Dependent Kinases; Cyclins; G1 Phase; Gene Expression Regulation; Neoplastic; Genes; Tumor Suppressor; Humans; Neoplasms; Proto-Oncogenes; Retinoblastoma Protein; S Phase; Signal Transduction; Tumor Suppressor Protein p53
Publication year: 1996
Journal or book title: Science
Volume: 274
Issue: 5293
Pages: 1672-1677
Find the full text: https://www.science.org/doi/abs/10.1126/science.274.5293.1672
Find more like this one (cited by): https://scholar.google.com/scholar?cites=2414071376079409726&as_sdt=1000005&sciodt=0,16&hl=en
Serial number: 3932