X-radiation enhances the collagen type I strap formation and migration potentials of colon cancer cells
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Stephanie Blockhuys1,3, Na Liu1, Nisha Rani Agarwal3, Annika Enejder3, Vesa Loitto2, Xiao-Feng Sun1
1Department of Oncology and Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden
2Medical Microbiology, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden
3Molecular Microscopy, Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden
Xiao-Feng Sun, email: email@example.com
Stephanie Blockhuys, email: firstname.lastname@example.org
Keywords: collagen type 1, colorectal cancer, X-radiation, cell migration, integrin β1
Received: March 17, 2016 Accepted: September 13, 2016 Published: September 19, 2016
Rectal cancer treatment still fails with local and distant relapses of the disease. It is hypothesized that radiotherapy could stimulate cancer cell dissemination and metastasis. In this study, we evaluated the effect of X-radiation on collagen type I strap formation potential, i.e. matrix remodeling associated with mesenchymal cell migration, and behaviors of SW480, SW620, HCT116 p53+/+ and HCT116 p53−/− colon cancer cells. We determined a radiation-induced increase in collagen type I strap formation and migration potentials of SW480 and HCT116 p53+/+. Further studies with HCT116 p53+/+, indicated that after X-radiation strap forming cells have an increased motility. More, we detected a decrease in adhesion potential and mature integrin β1 expression, but no change in non-muscle myosin II expression for HCT116 p53+/+ after X-radiation. Integrin β1 neutralization resulted in a decreased cell adhesion and collagen type I strap formation in both sham and X-radiated conditions. Our study indicates collagen type I strap formation as a potential mechanism of colon cancer cells with increased migration potential after X-radiation, and suggests that other molecules than integrin β1 and non-muscle myosin II are responsible for the radiation-induced collagen type I strap formation potential of colon cancer cells. This work encourages further molecular investigation of radiation-induced migration to improve rectal cancer treatment outcome.
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