
Fulltext:
109674.pdf
Embargo:
until further notice
Size:
2.669Mb
Format:
PDF
Description:
Publisher’s version
Publication year
2012Source
Cancer Research, 72, 16, (2012), pp. 4250-4261ISSN
Publication type
Article / Letter to editor

Display more detailsDisplay less details
Organization
Laboratory of Genetic, Endocrine and Metabolic Diseases
Paediatrics - OUD tm 2017
Cell Biology (UMC)
Pathology
Radiation Oncology
Journal title
Cancer Research
Volume
vol. 72
Issue
iss. 16
Page start
p. 4250
Page end
p. 4261
Subject
IGMD 6: Hormonal regulation ONCOL 5: Aetiology, screening and detection; NCMLS 4: Energy and redox metabolism IGMD 8: Mitochondrial medicine; ONCOL 2: Age-related aspects of cancer; ONCOL 2: Age-related aspects of cancer NCMLS 2: Immune Regulation; ONCOL 3: Translational researchAbstract
TRPM7 encodes a Ca(2+)-permeable nonselective cation channel with kinase activity. TRPM7 has been implicated in control of cell adhesion and migration, but whether TRPM7 activity contributes to cancer progression has not been established. Here we report that high levels of TRPM7 expression independently predict poor outcome in breast cancer patients and that it is functionally required for metastasis formation in a mouse xenograft model of human breast cancer. Mechanistic investigation revealed that TRPM7 regulated myosin II-based cellular tension, thereby modifying focal adhesion number, cell-cell adhesion and polarized cell movement. Our findings therefore suggest that TRPM7 is part of a mechanosensory complex adopted by cancer cells to drive metastasis formation. Cancer Res; 72(16); 4250-61. (c)2012 AACR.
This item appears in the following Collection(s)
- Academic publications [229134]
- Electronic publications [111496]
- Faculty of Medical Sciences [87758]
Upload full text
Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.