Gene expression profiling of luminal B breast cancers reveals NHERF1 as a new marker of endocrine resistance

Gene expression profiling of luminal B breast cancers reveals NHERF1 as a new marker of endocrine resistance

  • نوع فایل : کتاب
  • زبان : انگلیسی
  • مؤلف : Thomas Karn Eugen Ruckha¨berle Lars Hanker Volkmar Mu¨ ller Marcus Schmidt Christine Solbach Regine Ga¨tje Mathias Gehrmann Uwe Holtri
  • چاپ و سال / کشور: 2011

Description

The luminalBsubtype represents a group of high proliferating estrogen receptor positive breast cancers which are associated with a poor prognosis. Genes exclusively expressed in this subtype should help to better understand these tumors. In a finding cohort of 171 breast cancers luminal B specific genes were identified strong expression in highly proliferating Ki-67 positive/ER positive tumors but no expression either in Ki-67 negative/ER positive or in Ki-67 positive/ER negative samples. The clinical relevance of the scaffold protein NHERF1 identified by this strategy was assessed in a total of 3,030 breast cancers. NHERF1 expression was associated with the luminalBsubtype both in the finding and validation cohort. A positive correlation of NHERF1 expression with tumor size (P\0.001), grade (P\0.001), and HER2 status (P = 0.033) was observed. NHERF1 expression was associated with a worse survival in ER positive breast cancer (P\0.001) and retained its prognostic value in multivariate analysis. For ER positive samples with low NHERF1 expression a benefit of endocrine therapy was detected (P = 0.007). In contrast no differences in disease free survival were found for high NHERF1 expressing breast cancers which were either treated with endocrine therapy or no systemic therapy. Our data indicate that NHERF1 expressing breast cancers seem to have a greater risk to develop resistance to endocrine therapy. However, based on previous findings of NHERF1 functioning in PI3K signalling from basic research, these tumors might be appropriate candidates for a targeted therapy of the PI3K/Akt pathway.
DOI 10.1007/s10549-010-1333-x Received: 26 August 2010 / Accepted: 23 December 2010
اگر شما نسبت به این اثر یا عنوان محق هستید، لطفا از طریق "بخش تماس با ما" با ما تماس بگیرید و برای اطلاعات بیشتر، صفحه قوانین و مقررات را مطالعه نمایید.

دیدگاه کاربران


لطفا در این قسمت فقط نظر شخصی در مورد این عنوان را وارد نمایید و در صورتیکه مشکلی با دانلود یا استفاده از این فایل دارید در صفحه کاربری تیکت ثبت کنید.

بارگزاری