کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1929409 | 1050455 | 2012 | 5 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: ER-activating ability of breast cancer stromal fibroblasts is regulated independently of alteration of TP53 and PTEN tumor suppressor genes ER-activating ability of breast cancer stromal fibroblasts is regulated independently of alteration of TP53 and PTEN tumor suppressor genes](/preview/png/1929409.png)
Carcinoma-associated fibroblasts (CAFs) are associated with tumor progression and metastasis, and are able to activate estrogen receptor (ER) in breast cancer. We established a stable transformant of a human breast cancer cell line to detect CAF-specific ER-activating ability, and found that this CAF ability varied among tumors. Some studies have reported a high frequency of alterations among tumor suppressor genes in stromal cells, but do not generally agree as to the frequency. Moreover, the activation mechanism of CAF-induced estrogen signals, including the effects of these gene aberrations, is not fully understood. We investigated the relevance of tumor suppressor gene aberrations and ER-activating ability in CAFs derived from 20 breast cancer patients. Although CAF-specific ER-activating abilities varied among individual cases, all CAFs maintained wild-type alleles for TP53 and PTEN. Also, copy number aberrations in these genes were not observed in any CAFs. Our results suggest that the ER-activating ability of the CAFs is regulated independently of aberrations in these genes; and that other mechanisms of tumor–stromal interaction may affect activation of estrogen signals in breast cancer.
► Carcinoma-associated fibroblasts (CAFs) are able to activate estrogen receptor (ER) in breast cancer.
► CAF-specific ER-activating ability varied among individual cases.
► Breast CAFs maintained wild-type alleles for TP53 and PTEN.
► Copy number aberrations in these tumor suppressor genes were not observed in any CAFs.
► ER-activating ability of the CAFs is regulated independently of aberrations in these genes.
Journal: Biochemical and Biophysical Research Communications - Volume 428, Issue 2, 16 November 2012, Pages 259–263