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Genistein inhibits proliferation similarly in estrogen receptor-positive and negative human breast carcinoma cell lines characterized by P21WAF1/CIP1 induction, G2/M arrest, and apoptosis.
- Source :
-
Journal of cellular biochemistry [J Cell Biochem] 1998 Apr 01; Vol. 69 (1), pp. 44-54. - Publication Year :
- 1998
-
Abstract
- Genistein has been proposed to be responsible for lowering the rate of breast cancer in Asian women but the mechanism for this chemopreventive effect in vivo is unknown. In this study, we present in vitro evidence that genistein inhibits cell proliferation similarly in ER-positive and ER-negative human breast carcinoma cell lines. This inhibition is associated with specific G2/M arrest and induction of p21WAF1/CIP1 expression. Genistein results in a five-to six-fold increase in p21WAF1/CIP1 mRNA levels and a three- to four-fold increase in protein levels, only a 1.5-fold increase in p21WAF1/CIP1 transcription but a three- to six-fold increase in p21WAF1/CIP1 mRNA stability. The increase in p21WAF1/CIP1 is followed by increased apoptosis. The similar effects of genistein on a number of breast carcinoma cell lines with different ER and p53 status suggest that the actions of genistein reported here are mediated through ER and p53 independent mechanisms. The chemopreventive effects of genistein in vivo could be mediated along an identical or similar anti-proliferative pathway.
- Subjects :
- Apoptosis drug effects
Breast Neoplasms pathology
Cell Division drug effects
Cyclin-Dependent Kinase Inhibitor p21
Cyclins genetics
Female
G2 Phase drug effects
Gene Expression drug effects
Humans
Mitosis drug effects
Neoplasms, Hormone-Dependent pathology
RNA, Messenger genetics
RNA, Messenger metabolism
RNA, Neoplasm genetics
RNA, Neoplasm metabolism
Tumor Cells, Cultured
Antineoplastic Agents pharmacology
Breast Neoplasms drug therapy
Breast Neoplasms metabolism
Genistein pharmacology
Neoplasms, Hormone-Dependent drug therapy
Neoplasms, Hormone-Dependent metabolism
Receptors, Estrogen metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0730-2312
- Volume :
- 69
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Journal of cellular biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 9513045