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Inhibition of Hematopoietic Cell Kinase Activity Suppresses Myeloid Cell-Mediated Colon Cancer Progression

Authors :
Frederick Masson
Tracy L Putoczki
Oliver M. Sieber
Yelena Khakham
Cary Tsui
Lotta Burstroem
Ashleigh R Poh
Matthias Ernst
Clifford A. Lowell
Robert J.J. O'Donoghue
Adele Preaudet
Lachlan Whitehead
Guillaume Lessene
Simon Monard
Christopher G. Love
Olivia Newton-John Cancer Research Institute, La Trobe University School of Cancer Medicine, Heidelberg, VIC 3084, Australia
The Walter and Eliza Hall Institute of Medical Research, Department of Medical Biology, University of Melbourne, Melbourne, VIC 3052, Australia.
Source :
Cancer Cell, Cancer Cell, Elsevier, 2017, 31 (4), pp.563-575.e5. ⟨10.1016/j.ccell.2017.03.006⟩, Cancer cell, vol 31, iss 4
Publication Year :
2017

Abstract

International audience; 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.

Subjects

Subjects :
0301 basic medicine
MESH: Signal Transduction
Cancer Research
Colorectal cancer
[SDV]Life Sciences [q-bio]
Cell
Inbred C57BL
medicine.disease_cause
MESH: Mice, Knockout
Mice
0302 clinical medicine
tyrosine kinase inhibitor
2.1 Biological and endogenous factors
MESH: Animals
Src family kinase
Aetiology
Cancer
Mice, Knockout
MESH: STAT3 Transcription Factor
MESH: Macrophage Activation
Hematology
MESH: Gene Expression Regulation, Neoplastic
Colo-Rectal Cancer
3. Good health
Gene Expression Regulation, Neoplastic
medicine.anatomical_structure
colitis-associated colon cancer
hematopoietic cell kinase
Oncology
030220 oncology & carcinogenesis
Colonic Neoplasms
MESH: Pyrroles
Proto-Oncogene Proteins c-hck
Female
Signal transduction
Colorectal Neoplasms
MESH: Proto-Oncogene Proteins c-hck
alternative macrophage polarization
Signal Transduction
STAT3 Transcription Factor
MESH: Xenograft Model Antitumor Assays
Knockout
SRC family kinases
mouse model
Oncology and Carcinogenesis
colorectal cancer
Biology
stat3
Article
03 medical and health sciences
Rare Diseases
MESH: Mice, Inbred C57BL
medicine
tumor microenvironment
Animals
Humans
Pyrroles
Oncology & Carcinogenesis
xenograft
MESH: Colonic Neoplasms
Neoplastic
Tumor microenvironment
MESH: Humans
Oncogene
Neurosciences
Cell Biology
Macrophage Activation
medicine.disease
Xenograft Model Antitumor Assays
Mice, Inbred C57BL
030104 developmental biology
Pyrimidines
Gene Expression Regulation
MESH: Pyrimidines
Cancer research
MESH: Stromal Cells
Stromal Cells
Digestive Diseases
Carcinogenesis
MESH: Female
MESH: Colorectal Neoplasms

Details

Language :
English
ISSN :
15356108
Database :
OpenAIRE
Journal :
Cancer Cell, Cancer Cell, Elsevier, 2017, 31 (4), pp.563-575.e5. ⟨10.1016/j.ccell.2017.03.006⟩, Cancer cell, vol 31, iss 4
Accession number :
edsair.doi.dedup.....a1ccf5f96a12fd1b191d8e1ab5515751
Full Text :
https://doi.org/10.1016/j.ccell.2017.03.006⟩