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PMID: 12017312 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

The (-)-enantiomer of gossypol possesses higher anticancer potency than racemic gossypol in human breast cancer.

Anticancer research ·Vol. 22 ·No. 1A ·2002-00-00 ·Pages 33-8

Liu S, Kulp SK, Sugimoto Y, Jiang J, Chang HL, Dowd MK, Wan P, Lin YC

Abstract

Natural gossypol (GP), a polyphenolic pigment in cottonseed, is a racemic mixture of two enantiomers, (+)GP and (-)GP. Our aim was to compare the abilities of (+/-)GP, (+)GP and (-)GP to reduce proliferation of breast cancerous epithelial cells (cEC) and cancerous stromal cells (cSC). Proliferation was measured by 3H-thymidine uptake. Results showed that (+)GP had no effect on both cEC and cSC. In contrast, in both cell types, (+/-)GP and (-)GP significantly inhibited proliferation. (+/-)GP caused reductions of 15, 46 and 82% at 25, 5.0 and 7.5 microM, respectively, in cEC, and reductions of 17, 28, 39 and 56% at 2.0, 3.0, 4.0 and 5.0 microM, respectively, in cSC. (-)GP induced reductions of 33, 89 and 98% at 2.5, 5.0 and 7.5 microM, respectively, in cEC, and reductions of 29, 51, 64 and 72% at 2.0, 3.0, 4.0 and 5.0 microM, respectively, in cSC. By RT-PCR, we found that 3 microM of (+/-)GP and (-)GP decreased cyclin D1 mRNA expression in both cell types (52% and 71%, respectively, in cEC; and 47% and 71%, respectively, in cSC), and increased transforming growth factor beta (TGFbeta) mRNA expression in both cell types (93% and 130%, respectively, in cEC; and 45% and 89%, respectively, in cSC). Interestingly, (-)GP was significantly more potent than (+/-)GP. These results show that (-)GP is the major inhibitory component of (+/-)GP, (-)GP is the more potent inhibitor of cancerous breast cell growth, and the inhibitory activity of (-)GP and (+/-)GP is related to the reduction of the cell cycle regulator, cyclin D1, and the induction of the cell proliferation inhibitor, TGFbeta.

MeSH Terms
Breast Neoplasms/drug therapy,genetics,metabolism,pathology Cell Division/drug effects Cyclin D1/biosynthesis,genetics Dose-Response Relationship, Drug Drug Screening Assays, Antitumor Epithelial Cells/drug effects,pathology Gene Expression Regulation, Neoplastic/drug effects Gossypol/pharmacology Growth Inhibitors/pharmacology Humans RNA, Messenger/biosynthesis,genetics Stereoisomerism Stromal Cells/drug effects,pathology Transforming Growth Factor beta/biosynthesis,genetics Tumor Cells, Cultured
Chemicals
Growth Inhibitors RNA, Messenger Transforming Growth Factor beta Cyclin D1 Gossypol
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Liu Suling
Laboratory of Reproductive and Molecular Endocrinology, College of Veterinary Medicine, The Ohio State University, Columbus 43210, USA.
Kulp Samuel K
Sugimoto Yasuro
Jiang Jiahua
Chang Hsiang-Lin
Dowd Michael K
Wan Peter
Lin Young C
Article Info
Journal
Anticancer research
Abbr.
Anticancer Res
ISSN
0250-7005
Published
2002-00-00
Pages
33-8
Language
English
Region
Greece
NLM ID
8102988
Subset
IM
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