Elafin drives poor outcome in high-grade serous ovarian cancers and basal-like breast tumors View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2015-01

AUTHORS

S. Intidhar Labidi-Galy, Adam Clauss, Vivian Ng, Sekhar Duraisamy, Kevin M. Elias, Hui-Ying Piao, Erhan Bilal, Rachel A. Davidowitz, Yiling Lu, Gayane Badalian-Very, Balázs Györffy, Un-Beom Kang, Scott B. Ficarro, Shridar Ganesan, Gordon B. Mills, Jarrod A. Marto, Ronny Drapkin

ABSTRACT

High-grade serous ovarian carcinoma (HGSOC) and basal-like breast cancer (BLBC) share many features including TP53 mutations, genomic instability and poor prognosis. We recently reported that Elafin is overexpressed by HGSOC and is associated with poor overall survival. Here, we confirm that Elafin overexpression is associated with shorter survival in 1000 HGSOC patients. Elafin confers a proliferative advantage to tumor cells through the activation of the MAP kinase pathway. This mitogenic effect can be neutralized by RNA interference, specific antibodies and a MEK inhibitor. Elafin expression in patient-derived samples was also associated with chemoresistance and strongly correlates with bcl-xL expression. We extended these findings into the examination of 1100 primary breast tumors and six breast cancer cell lines. We observed that Elafin is overexpressed and secreted specifically by BLBC tumors and cell lines, leading to a similar mitogenic effect through activation of the MAP kinase pathway. Here too, Elafin overexpression is associated with poor overall survival, suggesting that it may serve as a biomarker and therapeutic target in this setting. More... »

PAGES

373

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/onc.2013.562

DOI

http://dx.doi.org/10.1038/onc.2013.562

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1010503310

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/24469047


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