| Literature DB >> 28399411 |
Ashleigh R Poh1, Christopher G Love2, Frederick Masson3, Adele Preaudet2, Cary Tsui2, Lachlan Whitehead2, Simon Monard2, Yelena Khakham2, Lotta Burstroem2, Guillaume Lessene4, Oliver Sieber5, Clifford Lowell6, Tracy L Putoczki1, Robert J J O'Donoghue7, Matthias Ernst8.
Abstract
Aberrant activation of the SRC family kinase hematopoietic cell kinase (HCK) triggers hematological malignancies as a tumor cell-intrinsic oncogene. Here we find that high HCK levels correlate with reduced survival of colorectal cancer patients. Likewise, increased Hck activity in mice promotes the growth of endogenous colonic malignancies and of human colorectal cancer cell xenografts. Furthermore, tumor-associated macrophages of the corresponding tumors show a pronounced alternatively activated endotype, which occurs independently of mature lymphocytes or of Stat6-dependent Th2 cytokine signaling. Accordingly, pharmacological inhibition or genetic reduction of Hck activity suppresses alternative activation of tumor-associated macrophages and the growth of colon cancer xenografts. Thus, Hck may serve as a promising therapeutic target for solid malignancies.Entities:
Keywords: SRC family kinases; alternative macrophage polarization; colitis-associated colon cancer; colorectal cancer; hematopoietic cell kinase; mouse model; stat3; tumor microenvironment; tyrosine kinase inhibitor; xenograft
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Year: 2017 PMID: 28399411 PMCID: PMC5479329 DOI: 10.1016/j.ccell.2017.03.006
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743