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进行cDNA转染,随后分离出在体外和体内对他莫昔芬耐药的MCF-7乳腺癌细胞系。

cDNA transfection followed by the isolation of a MCF-7 breast cell line resistant to tamoxifen in vitro and in vivo.

作者信息

Toi M, Harris A L, Bicknell R

机构信息

Molecular Oncology Laboratory, Imperial Cancer Research Fund, University of Oxford, John Radcliffe Hospital, UK.

出版信息

Br J Cancer. 1993 Dec;68(6):1088-96. doi: 10.1038/bjc.1993.486.

Abstract

A tamoxifen resistant cell line (clone 9) has been isolated from the tamoxifen sensitive, hormone responsive MCF-7 breast carcinoma cell line after transfection with mixed cDNA libraries, followed by tamoxifen selection in the presence of oestrogens. Transfection was confirmed by Southern analysis with vector probes. Clone 9 in several-fold more resistant to tamoxifen and other anti-oestrogens than wild type cells when cultured either as a monolayer or as colonies in soft agar but retains oestrogen receptors. Clone 9 was less responsive to 17-beta-oestradiol than were wild type MCF-7. In addition to showing in vitro tamoxifen resistance, clone 9 was also tamoxifen resistant in vivo when xenografted into the nude mouse. Culture medium conditioned by clone 9 cells stimulated quiescent cells of the same clone as well as wild type cells, whereas medium conditioned by wild type MCF-7 was inhibitory to both, suggesting that clone 9 may be secreting an autocrine growth factor. Clone 9 provides a novel model for further investigation of the mechanism of anti-oestrogen resistance that occurs without loss of oestrogen receptors. Preliminary results suggest that an autocrine growth stimulatory mechanism may be one pathway of such resistance.

摘要

从对他莫昔芬敏感、激素反应性的MCF - 7乳腺癌细胞系中,通过用混合cDNA文库转染,随后在雌激素存在下进行他莫昔芬筛选,分离出了一种他莫昔芬耐药细胞系(克隆9)。用载体探针进行Southern分析证实了转染。当以单层培养或在软琼脂中形成集落培养时,克隆9对他莫昔芬和其他抗雌激素的耐药性比野生型细胞高几倍,但仍保留雌激素受体。克隆9对17-β-雌二醇的反应性低于野生型MCF - 7。除了在体外表现出对他莫昔芬的耐药性外,克隆9异种移植到裸鼠体内时对他莫昔芬也具有耐药性。由克隆9细胞条件培养基刺激相同克隆的静止细胞以及野生型细胞,而野生型MCF - 7的条件培养基对两者均有抑制作用,这表明克隆9可能分泌一种自分泌生长因子。克隆9为进一步研究在不丧失雌激素受体的情况下发生的抗雌激素耐药机制提供了一个新模型。初步结果表明,自分泌生长刺激机制可能是这种耐药性的一条途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e82/1968663/cb2b0308ae7b/brjcancer00202-0046-a.jpg

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