Isolation of the human anionic glutathione S-transferase cDNA and the relation of its gene expression to estrogen-receptor content in primary breast cancer

J. A. Moscow, A. J. Townsend, M. E. Goldsmith, J. Whang-Peng, P. J. Vickers, R. Poisson, S. Legault-Poisson, C. E. Myers, K. H. Cowan

研究成果: 雜誌貢獻文章

114 引文 (Scopus)

摘要

The development of multidrug resistance in MCF7 human breast cancer cells is associated with overexpression of P-glycoprotein, changes in activities of several detoxication enzymes, and loss of hormone sensitivity and estrogen receptors (ERs). We have cloned the cDNA for one of the drug-detoxifying enzymes overexpressed in multidrug-resistant MCF7 cells (Adr(R) MCF7) , the anionic isozyme of glutathione S-transferase (GSTπ). Hybridization with this GSTπ cDNA, GSTπ-1, demonstrated that increased GSTπ activity in Adr(R) MCF7 cells is associated with overexpression but not with amplification of the gene. We mapped the GSTπ gene to human chromosome 11q13 by in situ hybridization. Since multidrug resistance and GSTπ overexpression are associated with the loss of ERs in Adr(R) MCF7 cells, we examined several other breast cancer cell lines that were not selected for drug resistance. In each of these cell lines we found an inverse association between GSTπ expression and ER content. We also examined RNA from 21 primary breast cancers and found a similar association between GSTπ expression and ER content in vivo. GSTπ mRNA content in 11 ER-positive tumors (≤10 fmol/mg of protein) was significantly different from the GSTπ content of 10 ER-negative tumors (P = 0.002; Mann-Whitney Wilcoxon test for two independent samples). The finding of similar patterns of expression of a drug-detoxifying enzyme and of ERs in vitro as well as in vivo suggests that ER-negative breast cancer cells may have greater protection against antineoplastic agents conferred by GSTπ than ER-positive tumors.
原文英語
頁(從 - 到)6518-6522
頁數5
期刊Proceedings of the National Academy of Sciences of the United States of America
85
發行號17
DOIs
出版狀態已發佈 - 一月 1 1988
對外發佈Yes

指紋

Glutathione Transferase
Estrogen Receptors
Complementary DNA
Breast Neoplasms
Gene Expression
MCF-7 Cells
Multiple Drug Resistance
Enzymes
Cell Line
Neoplasms
Gene Amplification
Human Chromosomes
P-Glycoprotein
Drug Resistance
Pharmaceutical Preparations
Antineoplastic Agents
Isoenzymes
In Situ Hybridization
Hormones
RNA

ASJC Scopus subject areas

  • General

引用此文

Isolation of the human anionic glutathione S-transferase cDNA and the relation of its gene expression to estrogen-receptor content in primary breast cancer. / Moscow, J. A.; Townsend, A. J.; Goldsmith, M. E.; Whang-Peng, J.; Vickers, P. J.; Poisson, R.; Legault-Poisson, S.; Myers, C. E.; Cowan, K. H.

於: Proceedings of the National Academy of Sciences of the United States of America, 卷 85, 編號 17, 01.01.1988, p. 6518-6522.

研究成果: 雜誌貢獻文章

Moscow, J. A. ; Townsend, A. J. ; Goldsmith, M. E. ; Whang-Peng, J. ; Vickers, P. J. ; Poisson, R. ; Legault-Poisson, S. ; Myers, C. E. ; Cowan, K. H. / Isolation of the human anionic glutathione S-transferase cDNA and the relation of its gene expression to estrogen-receptor content in primary breast cancer. 於: Proceedings of the National Academy of Sciences of the United States of America. 1988 ; 卷 85, 編號 17. 頁 6518-6522.
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abstract = "The development of multidrug resistance in MCF7 human breast cancer cells is associated with overexpression of P-glycoprotein, changes in activities of several detoxication enzymes, and loss of hormone sensitivity and estrogen receptors (ERs). We have cloned the cDNA for one of the drug-detoxifying enzymes overexpressed in multidrug-resistant MCF7 cells (Adr(R) MCF7) , the anionic isozyme of glutathione S-transferase (GSTπ). Hybridization with this GSTπ cDNA, GSTπ-1, demonstrated that increased GSTπ activity in Adr(R) MCF7 cells is associated with overexpression but not with amplification of the gene. We mapped the GSTπ gene to human chromosome 11q13 by in situ hybridization. Since multidrug resistance and GSTπ overexpression are associated with the loss of ERs in Adr(R) MCF7 cells, we examined several other breast cancer cell lines that were not selected for drug resistance. In each of these cell lines we found an inverse association between GSTπ expression and ER content. We also examined RNA from 21 primary breast cancers and found a similar association between GSTπ expression and ER content in vivo. GSTπ mRNA content in 11 ER-positive tumors (≤10 fmol/mg of protein) was significantly different from the GSTπ content of 10 ER-negative tumors (P = 0.002; Mann-Whitney Wilcoxon test for two independent samples). The finding of similar patterns of expression of a drug-detoxifying enzyme and of ERs in vitro as well as in vivo suggests that ER-negative breast cancer cells may have greater protection against antineoplastic agents conferred by GSTπ than ER-positive tumors.",
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AU - Moscow, J. A.

AU - Townsend, A. J.

AU - Goldsmith, M. E.

AU - Whang-Peng, J.

AU - Vickers, P. J.

AU - Poisson, R.

AU - Legault-Poisson, S.

AU - Myers, C. E.

AU - Cowan, K. H.

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N2 - The development of multidrug resistance in MCF7 human breast cancer cells is associated with overexpression of P-glycoprotein, changes in activities of several detoxication enzymes, and loss of hormone sensitivity and estrogen receptors (ERs). We have cloned the cDNA for one of the drug-detoxifying enzymes overexpressed in multidrug-resistant MCF7 cells (Adr(R) MCF7) , the anionic isozyme of glutathione S-transferase (GSTπ). Hybridization with this GSTπ cDNA, GSTπ-1, demonstrated that increased GSTπ activity in Adr(R) MCF7 cells is associated with overexpression but not with amplification of the gene. We mapped the GSTπ gene to human chromosome 11q13 by in situ hybridization. Since multidrug resistance and GSTπ overexpression are associated with the loss of ERs in Adr(R) MCF7 cells, we examined several other breast cancer cell lines that were not selected for drug resistance. In each of these cell lines we found an inverse association between GSTπ expression and ER content. We also examined RNA from 21 primary breast cancers and found a similar association between GSTπ expression and ER content in vivo. GSTπ mRNA content in 11 ER-positive tumors (≤10 fmol/mg of protein) was significantly different from the GSTπ content of 10 ER-negative tumors (P = 0.002; Mann-Whitney Wilcoxon test for two independent samples). The finding of similar patterns of expression of a drug-detoxifying enzyme and of ERs in vitro as well as in vivo suggests that ER-negative breast cancer cells may have greater protection against antineoplastic agents conferred by GSTπ than ER-positive tumors.

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