Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/19002
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dc.contributor.authorPoh, Ashleigh R-
dc.contributor.authorLove, Christopher G-
dc.contributor.authorMasson, Frederic-
dc.contributor.authorPreaudet, Adele-
dc.contributor.authorTsui, Cary-
dc.contributor.authorWhitehead, Lachlan-
dc.contributor.authorMonard, Simon-
dc.contributor.authorKhakham, Yelena-
dc.contributor.authorBurstroem, Lotta-
dc.contributor.authorLessene, Guillaume-
dc.contributor.authorSieber, Oliver-
dc.contributor.authorLowell, Clifford-
dc.contributor.authorPutoczki, Tracy L-
dc.contributor.authorO'Donoghue, Robert J J-
dc.contributor.authorErnst, Matthias-
dc.date.accessioned2018-09-12T23:57:45Z-
dc.date.available2018-09-12T23:57:45Z-
dc.date.issued2017-04-10-
dc.identifier.citationCancer cell 2017; 31(4): 563-575.e5-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/19002-
dc.description.abstractAberrant 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.-
dc.language.isoeng-
dc.subjectSRC family kinases-
dc.subjectAlternative macrophage polarization-
dc.subjectColitis-associated colon cancer-
dc.subjectColorectal cancer-
dc.subjectHematopoietic cell kinase-
dc.subjectMouse model-
dc.subjectstat3-
dc.subjecttumor microenvironment-
dc.subjecttyrosine kinase inhibitor-
dc.subjectxenograft-
dc.titleInhibition of Hematopoietic Cell Kinase Activity Suppresses Myeloid Cell-Mediated Colon Cancer Progression.-
dc.typeJournal Article-
dc.identifier.journaltitleCancer cell-
dc.identifier.affiliationOlivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationSchool of Cancer Medicine, La Trobe University, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Pathology and Laboratory Medicine, University of California, San Francisco, CA 94143, USAen
dc.identifier.affiliationDepartment of Pharmacology and Therapeutics, University of Melbourne, Melbourne, VIC 3010, Australiaen
dc.identifier.affiliationDepartment of Colorectal Surgery, Royal Melbourne Hospital, Melbourne, VIC 3050, Australiaen
dc.identifier.affiliationSchool of Biomedical Sciences, Monash University, Clayton, VIC 3800, Australiaen
dc.identifier.affiliationThe Walter and Eliza Hall Institute of Medical Research, Department of Medical Biology, University of Melbourne, Melbourne, VIC 3052, Australiaen
dc.identifier.doi10.1016/j.ccell.2017.03.006-
dc.identifier.pubmedid28399411-
dc.type.austinJournal Article-
dc.type.austinResearch Support, Non-U.S. Gov't-
local.name.researcherErnst, Matthias
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
Appears in Collections:Journal articles
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