ENHANCED GROWTH OF MAMMARY ADENOCARCINOMA IN RATS BY CHLOROQUINE AND QUINACRINE

被引:4
作者
DUTTA, P
KARMALI, R
PINTO, JT
RIVLIN, RS
机构
[1] Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY 10021
关键词
MAMMARY TUMORS; CARCINOGENESIS; CHLOROQUINE; QUINACRINE; PROSTAGLANDINS; GLUTATHIONE; RIBOFLAVIN;
D O I
10.1016/0304-3835(94)90386-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study investigated whether the growth of transplanted mammary tumors is altered in rats by treatment with the antimalarial drugs chloroquine (CQ) and quinacrine (QN). Female inbred F344 rats were divided into three experimental groups. Animals were injected i.p. with either CQ, QN or normal saline for 5 days a week throughout the entire experimental period (25 days). After 7 days of drug treatment each rat received subcutaneously one 2-mm(2) aliquot of R3230AC mammary adenocarcinoma in the mid-thoracic region. Eighteen days after implantation, all rats were sacrificed and tumors were excised, weighed and measured. The results indicate that weights and volumes of tumors as well as tumor-to-body weight ratios were significantly higher in CQ and QN-treated animals than those in saline-treated animals. The final body weights of rats treated with QN were significantly lower than those treated with saline. The prostaglandin E(2) content of tumors was significantly reduced by CQ treatment. Erythrocyte glutathione reductase activity coefficient and reduced glutathione concentrations remained unaffected by both treatments. These results suggest that CQ and QN have significant stimulatory effects on the growth of mammary adenocarcinoma in rats.
引用
收藏
页码:113 / 119
页数:7
相关论文
共 33 条
[1]   QUINACRINE HYDROCHLORIDE DRUG ERUPTION (TROPICAL LICHENOID DERMATITIS) - ITS EARLY AND LATE SEQUELAE AND ITS MALIGNANT POTENTIAL - A REVIEW [J].
BAUER, F .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1981, 4 (02) :239-248
[2]   CANCER GROWTH, RESPONSE TO TREATMENT AND SURVIVAL TIME IN MICE - BENEFICIAL EFFECT OF THE PROSTAGLANDIN SYNTHESIS INHIBITOR FLURBIPROFEN [J].
BENNETT, A ;
HOUGHTON, J ;
LEAPER, DJ ;
STAMFORD, IF .
PROSTAGLANDINS, 1979, 17 (02) :179-191
[4]  
Beutler E., 1971, RED CELL METABOLISM, P103
[5]   ANTI-RHEUMATIC DRUGS AND MACROPHAGE FUNCTION - EFFECTS ON TUMOR-CELL GROWTH-INVITRO [J].
BINDERUP, L ;
BRAMM, E ;
ARRIGONIMARTELLI, E .
CLINICAL RHEUMATOLOGY, 1982, 1 (01) :15-22
[6]   BURKITT LYMPHOMA IN PAPUA NEW GUINEA [J].
BOOTH, K ;
BURKITT, DP ;
BASSETT, DJ ;
COOKE, RA ;
BIDDULPH, J .
BRITISH JOURNAL OF CANCER, 1967, 21 (04) :657-&
[7]   CHILDRENS CANCER DEPENDENT ON CLIMATIC FACTORS [J].
BURKITT, D .
NATURE, 1962, 194 (4825) :232-&
[8]   RIBOFLAVIN DEFICIENCY AND GLUTATHIONE METABOLISM IN RATS - POSSIBLE MECHANISMS UNDERLYING ALTERED RESPONSES TO HEMOLYTIC STIMULI [J].
DUTTA, P ;
GEE, M ;
RIVLIN, RS ;
PINTO, J .
JOURNAL OF NUTRITION, 1988, 118 (09) :1149-1157
[9]  
DUTTA P, 1987, FLAVINS FLAVOPROTEIN, P473
[10]  
ERTEL W, 1991, BLOOD, V78, P1781