BCAR1/p130Cas expression in untreated and acquired tamoxifen‐resistant human breast carcinomas

High BCAR1/p130Cas expression in primary breast tumour cytosol predicts a poor chance of response recurrent disease to tamoxifen treatment in patients with oestrogen receptor (ER)–positive breast carcinomas. In this study, we assessed whether BCAR1/p130Cas expression is altered during acquisition of...

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Veröffentlicht in:International journal of cancer 2000-09, Vol.89 (5), p.465-468
Hauptverfasser: van der Flier, Silvia, Chan, Christina M.W., Brinkman, Arend, Smid, Marcel, Johnston, Stephen R.D., Dorssers, Lambert C.J., Dowsett, Mitchell
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Sprache:eng
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Zusammenfassung:High BCAR1/p130Cas expression in primary breast tumour cytosol predicts a poor chance of response recurrent disease to tamoxifen treatment in patients with oestrogen receptor (ER)–positive breast carcinomas. In this study, we assessed whether BCAR1/p130Cas expression is altered during acquisition of anti‐oestrogen resistance. BCAR1/p130Cas protein was quantitatively measured by chemiluminescent Western blot analysis in the cytosol of 34 predominantly ER+ carcinomas that initially responded to primary tamoxifen treatment and subsequently progressed (n = 22 ) or developed during adjuvant tamoxifen treatment (n = 12) and compared to 54 untreated ER+ human breast carcinomas. We did not detect significant differences in the level of BCAR1/p130Cas protein in untreated and acquired tamoxifen‐resistant carcinomas. Our results indicate that in tumour progression towards tamoxifen resistance, increase of BCAR1/p130Cas may be only one of the molecular mechanisms. Thus, high BCAR1/p130Cas protein levels appear to be a hallmark for intrinsic resistance to tamoxifen in breast carcinomas. Int. J. Cancer 89:465–468, 2000. © 2000 Wiley‐Liss, Inc.
ISSN:0020-7136
1097-0215
DOI:10.1002/1097-0215(20000920)89:5<465::AID-IJC11>3.0.CO;2-O