Global quantitative phosphoproteome analysis of human tumor xenografts treated with a CD44 antagonist

S Weigand, F Herting, D Maisel, A Nopora, E Voss… - Cancer research, 2012 - AACR
S Weigand, F Herting, D Maisel, A Nopora, E Voss, C Schaab, M Klammer, A Tebbe
Cancer research, 2012AACR
The cell surface glycoprotein CD44 plays an important role in the development and
progression of various tumor types. RG7356 is a humanized antibody targeting the constant
region of CD44 that shows antitumor efficacy in mice implanted with CD44-expressing
tumors such as MDA-MB-231 breast cancer cells. CD44 receptor seems to function as the
main receptor for hyaluronic acid and osteopontin, serving as coreceptor for growth factor
pathways like cMet, EGFR, HER-2, and VEGFR and by cytoskeletal modulation via ERM and …
Abstract
The cell surface glycoprotein CD44 plays an important role in the development and progression of various tumor types. RG7356 is a humanized antibody targeting the constant region of CD44 that shows antitumor efficacy in mice implanted with CD44-expressing tumors such as MDA-MB-231 breast cancer cells. CD44 receptor seems to function as the main receptor for hyaluronic acid and osteopontin, serving as coreceptor for growth factor pathways like cMet, EGFR, HER-2, and VEGFR and by cytoskeletal modulation via ERM and Rho kinase signaling. To assess the direct impact of RG7356 binding to the CD44 receptor, a global mass spectrometry–based phosphoproteomics approach was applied to freshly isolated MDA-MB-231 tumor xenografts. Results from a global phosphoproteomics screen were further corroborated by Western blot and ELISA analyses of tumor lysates from CD44-expressing tumors. Short-term treatment of tumor-bearing mice with RG7356 resulted in modifications of the MAPK pathway in the responsive model, although no effects on downstream phosphorylation were observed in a nonresponsive xenograft model. Taken together, our approach augments the value of other high throughput techniques to identify biomarkers for clinical development of targeted agents. Cancer Res; 72(17); 4329–39. ©2012 AACR.
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