ANTIPROLIFERATIVE ACTIVITY OF GOSSYPOL AND GOSSYPOLONE ON HUMAN BREAST-CANCER CELLS

被引:112
作者
GILBERT, NE
OREILLY, JE
CHANG, CJG
LIN, YC
BRUEGGEMEIER, RW
机构
[1] OHIO STATE UNIV, COLL PHARM, DIV MED CHEM & PHARMACOGNOSY, COLUMBUS, OH 43210 USA
[2] OHIO STATE UNIV, COLL VET MED, DEPT VET BIOSCI, COLUMBUS, OH 43210 USA
[3] OHIO STATE UNIV, CTR COMPREHENS CANC, COLUMBUS, OH 43210 USA
关键词
GOSSYPOL; GOSSYPOLONE; HUMAN MAMMARY CARCINOMA CELL CULTURE; BREAST CANCER;
D O I
10.1016/0024-3205(95)00243-Y
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Gossypol is a polyphenolic aldehyde occurring naturally in cottonseed that produces antisteroidogenic activity in vivo, has been extensively investigated as a male contraceptive agent, and has demonstrated anticancer activity. Gossypolone, the major metabolite of gossypol, also prossesses antisteroidogenic activity but has not been examined for its anticancer properties. The objectives of these investigations are to compare the effects of gossypolone with those of gossypol on cell proliferation of hormone-dependent and hormone-independent human breast carcinoma cells, i.e., MCF-7, MCF-7(Adr) and MDA-MB-231 cells. Gossypol and gossypolone were examined at concentrations upto 10 mu M, and cellular DNA synthesis was monitored by H-3-thymidine incorporation. Gossypol and gossypolone produced dose-dependent suppression of DNA synthesis in all of the human breast cell lines examined. Gossypol produced potent antiproliferative activity in MCF-7 cells at doses as low as 30 nM. Co-incubation of MCF-7 cells with gossypol (5 mu M) and estradiol (10 nM) did not alter the effects of gossypol. Treatment of human breast cancer cells with 2.5 mu M of gossypol resulted in alterations in cell shape and attachment to the surface of the culture dishes. At gossypol doses of 10 mu M, pericytoplasmic globuation and cytoplasmic swelling were observed in the majority of breast cancer cells. These changes in cellular morphology indicate a loss of ability of the cells to maintain normal cell membrane permeability, resulting in subsequent disorganization and loss of cytoplasmic organelles. Gossypolone is less potent than gossypol in producing these effects in the human breast cancer cell lines, whereas it possesses equipotent antisteroidogenic and antireproductive activities with gossypol. These investigations suggest that gossypol and gossypol analogs may have therapeutic potential for human breast cancer.
引用
收藏
页码:61 / 67
页数:7
相关论文
共 32 条
[21]  
LIN YC, 1985, ADV CONTR DELIV SYST, V2, P200
[22]  
MODICANAPOLITANO JS, 1987, CANCER RES, V47, P4361
[23]  
MOH PP, 1992, RES COMMUN CHEM PATH, V76, P305
[24]   KINETICS OF GOSSYPOL INHIBITION OF BOVINE LACTATE DEHYDROGENASE-X [J].
OLGIATI, KL ;
TOSCANO, WA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1983, 115 (01) :180-185
[25]   GOSSYPOL INHIBITION OF ADENYLATE-CYCLASE [J].
OLGIATI, KL ;
TOSCANO, DG ;
ATKINS, WM ;
TOSCANO, WA .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1984, 231 (02) :411-415
[26]  
RAO PN, 1985, CANCER CHEMOTH PHARM, V15, P20
[27]  
SEGAL SJ, 1985, GOSSYPOL POTENTIAL C
[28]   UNUSUAL RETENTION OF RHODAMINE-123 BY MITOCHONDRIA IN MUSCLE AND CARCINOMA-CELLS [J].
SUMMERHAYES, IC ;
LAMPIDIS, TJ ;
BERNAL, SD ;
NADAKAVUKAREN, JJ ;
NADAKAVUKAREN, KK ;
SHEPHERD, EL ;
CHEN, LB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (17) :5292-5296
[29]  
WANG NG, 1987, J ETHNOPHARMACOL, V20, P45
[30]  
WANG YC, 1984, CANCER RES, V44, P35