The cocaine- and amphetamine-regulated transcript mediates ligand-independent activation of ER alpha, and is an independent prognostic factor in node-negative breast cancer

التفاصيل البيبلوغرافية
العنوان: The cocaine- and amphetamine-regulated transcript mediates ligand-independent activation of ER alpha, and is an independent prognostic factor in node-negative breast cancer
المؤلفون: Brennan, D. J., O'Connor, D. P., Laursen, H., McGee, S. F., McCarthy, S., Zagozdzon, R., Rexhepaj, E., Culhane, A. C., Martin, F. M., Duffy, M. J., Landberg, Göran, Rydén, Lisa, Hewitt, S. M., Kuhar, M. J., Bernards, R., Millikan, R. C., Crown, J. P., Jirström, Karin, Gallagher, W. M.
المصدر: Oncogene BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation. 31(30):3483-3494
مصطلحات موضوعية: cocaine- and amphetamine-regulated transcript, breast cancer, prognosis, estrogen receptor, Medicin och hälsovetenskap, Klinisk medicin, Cancer och onkologi, Medical and Health Sciences, Clinical Medicine, Cancer and Oncology
الوصف: Personalized medicine requires the identification of unambiguous prognostic and predictive biomarkers to inform therapeutic decisions. Within this context, the management of lymph node-negative breast cancer is the subject of much debate with particular emphasis on the requirement for adjuvant chemotherapy. The identification of prognostic and predictive biomarkers in this group of patients is crucial. Here, we demonstrate by tissue microarray and automated image analysis that the cocaine- and amphetamine-regulated transcript (CART) is expressed in primary and metastatic breast cancer and is an independent poor prognostic factor in estrogen receptor (ER)-positive, lymph node-negative tumors in two separate breast cancer cohorts (n = 690; P = 0.002, 0.013). We also show that CART increases the transcriptional activity of ER alpha in a ligand-independent manner via the mitogen-activated protein kinase pathway and that CART stimulates an autocrine/paracrine loop within tumor cells to amplify the CART signal. Additionally, we demonstrate that CART expression in ER-positive breast cancer cell lines protects against tamoxifen-mediated cell death and that high CART expression predicts disease outcome in tamoxifen-treated patients in vivo in three independent breast cancer cohorts. We believe that CART profiling will help facilitate stratification of lymph node-negative breast cancer patients into high- and low-risk categories and allow for the personalization of therapy. Oncogene (2012) 31, 3483-3494; doi:10.1038/onc.2011.519; published online 5 December 2011
الوصول الحر: https://lup.lub.lu.se/record/3070000Test
http://dx.doi.org/10.1038/onc.2011.519Test
قاعدة البيانات: SwePub
الوصف
تدمد:14765594
DOI:10.1038/onc.2011.519