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他莫昔芬治疗后人体乳腺癌组织中转化生长因子β1的体内诱导作用

Induction of transforming growth factor beta 1 in human breast cancer in vivo following tamoxifen treatment.

作者信息

Butta A, MacLennan K, Flanders K C, Sacks N P, Smith I, McKinna A, Dowsett M, Wakefield L M, Sporn M B, Baum M

机构信息

Hartwell Laboratory Royal Marsden Hospital, London, United Kingdom.

出版信息

Cancer Res. 1992 Aug 1;52(15):4261-4.

PMID:1322240
Abstract

We have investigated the ability of tamoxifen to regulate members of the transforming growth factor beta (TGF-beta) family in human breast cancers in vivo. Using immunohistochemical techniques, we find that 3 months of tamoxifen treatment causes a consistent induction of extracellular TGF-beta 1 in breast cancer biopsies, compared with matched pretreatment samples from the same patient. The induced TGF-beta is localized between and around stromal fibroblasts and appears to be derived from these cells. Lower levels of TGF-beta 1,-beta 2, and -beta 3 seen in epithelial cells were not altered by tamoxifen treatment. The increased stromal staining of TGF-beta 1 occurred in estrogen receptor-negative as well as estrogen receptor-positive tumors. These results provide in vivo evidence for a novel, estrogen receptor-independent mechanism of action for tamoxifen, involving the stromal induction of a potent growth inhibitor for epithelial cells.

摘要

我们研究了他莫昔芬在体内调节人乳腺癌中转化生长因子β(TGF-β)家族成员的能力。使用免疫组织化学技术,我们发现与来自同一患者的配对预处理样本相比,他莫昔芬治疗3个月会导致乳腺癌活检组织中细胞外TGF-β1持续诱导。诱导的TGF-β定位于基质成纤维细胞之间和周围,似乎来源于这些细胞。他莫昔芬治疗并未改变上皮细胞中较低水平的TGF-β1、-β2和-β3。TGF-β1的基质染色增加发生在雌激素受体阴性以及雌激素受体阳性肿瘤中。这些结果为他莫昔芬的一种新的、雌激素受体非依赖性作用机制提供了体内证据,该机制涉及基质诱导上皮细胞的一种强效生长抑制剂。

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