NIOSHTIC-2 Publications Search

G1 cell cycle progression and the expression of G1 cyclins are regulated by PI3K/AKT/mTOR/p70S6K1 signaling in human ovarian cancer cells.

Gao N; Flynn DC; Zhang Z; Zhong XS; Walker V; Liu KJ; Shi X; Jiang BH
Am J Physiol, Cell Physiol 2004 Aug; 287(2):C281-C291
Ovarian cancer is one of the most common cancers among women. Recent studies demonstrated that the gene encoding the p110a catalytic subunit of phosphatidylinositol 3-kinase (PI3K) is frequently amplified in ovarian cancer cells. PI3K is involved in multiple cellular functions, including proliferation, differentiation, antiapoptosis, tumorigenesis, and angiogenesis. In this study, we demonstrate that the inhibition of PI3K activity by LY-294002 inhibited ovarian cancer cell proliferation and induced G1 cell cycle arrest. This effect was accompanied by the decreased expression of G1-associated proteins, including cyclin D1, cyclin-dependent kinase (CDK) 4, CDC25A, and retinoblastoma phosphorylation at Ser780, Ser795, and Ser807/811. Expression of CDK6 and B-actin was not affected by LY-294002. Expression of the cyclin kinase inhibitor p16INK4a was induced by the PI3K inhibitor, whereas steady-state levels of p21CIP1/WAF1 were decreased in the same experiment. The inhibition of PI3K activity also inhibited the phosphorylation of AKT and p70S6K1, but not extracellular regulated kinase 1/2. The G1 cell cycle arrest induced by LY-294002 was restored by the expression of active forms of AKT and p70S6K1 in the cells. Our study shows that PI3K transmits a mitogenic signal through AKT and mammalian target of rapamycin (mTOR) to p70S6K1. The mTOR inhibitor rapamycin had similar inhibitory effects on G1 cell cycle progression and on the expression of cyclin D1, CDK4, CDC25A, and retinoblastoma phosphorylation. These results indicate that PI3K mediates G1 progression and cyclin expression through activation of an AKT/mTOR/p70S6K1 signaling pathway in the ovarian cancer cells.
Cancer; Demographic-characteristics; Sex-factors; Cell-function; Cellular-function; Cell-differentiation; Tumorigenesis; Cell-cultures
Publication Date
Document Type
Journal Article
Email Address
Fiscal Year
Issue of Publication
NIOSH Division
Source Name
American Journal of Physiology: Cell Physiology
Page last reviewed: December 30, 2021
Content source: National Institute for Occupational Safety and Health Education and Information Division