Cancer-associated fibroblasts from human NSCLC survive ablative doses of radiation but their invasive capacity is reduced

Hellevik, T. et al. (2012) Cancer-associated fibroblasts from human NSCLC survive ablative doses of radiation but their invasive capacity is reduced. Radiation Oncology, 7(59), (doi: 10.1186/1748-717X-7-59)

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Publisher's URL: http://dx.doi.org/10.1186/1748-717X-7-59

Abstract

<p>Background: Cancer-Associated Fibroblasts (CAFs) are significant components of solid malignancies and play central roles in cancer sustainability, invasion and metastasis. In this study we have investigated the invasive capacity and matrix remodelling properties of human lung CAFs after exposure to ablative doses of ionizing radiation (AIR), equivalent to single fractions delivered by stereotactic ablative radiotherapy (SART) for medically inoperable stage-I/II non-small-cell lung cancers.</p> <p>Methods: CAFs were isolated from lung tumour specimens from 16 donors. Initially, intrinsic radiosensitivity was evaluated by checking viability and extent of DNA-damage response (DDR) at different radiation doses. The migrative and invasive capacities of CAFs were thereafter determined after a sub-lethal single radiation dose of 18 Gy. To ascertain the mechanisms behind the altered invasive capacity of cells, expression of matrix metalloproteinases (MMPs) and their endogenous inhibitors (TIMPs) were measured in the conditioned media several days post-irradiation, along with expression of cell surface integrins and dynamics of focal contacts by vinculin-staining.</p> <p>Results: Exposing CAFs to 1 × 18 Gy resulted in a potent induction of multiple nuclear DDR foci (> 9/cell) with little resolution after 120 h, induced premature cellular senescence and inhibition of the proliferative, migrative and invasive capacity. AIR promoted MMP-3 and inhibited MMP-1 appearance to some extent, but did not affect expression of other major MMPs. Furthermore, surface expression of integrins α2, β1 and α5 was consistently enhanced, and a dramatic augmentation and redistribution of focal contacts was observed.</p> <p>Conclusions: Our data indicate that ablative doses of radiation exert advantageous inhibitory effects on the proliferative, migratory and invasive capacity of lung CAFs. The reduced motility of irradiated CAFs might be a consequence of stabilized focal contacts via integrins.</p>

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Chalmers, Professor Anthony
Authors: Hellevik, T., Pettersen, I., Berg, V., Winberg, J. O., Moe, B. T., Bartnes, K., Paulssen, R. H., Busund, L.-T., Bremnes, R., Chalmers, A., and Martinez-Zubiaurre, I.
College/School:College of Medical Veterinary and Life Sciences > School of Cancer Sciences
Journal Name:Radiation Oncology
Publisher:BioMed Central
ISSN:1748-717X
Copyright Holders:Copyright © 2012 The Authors
First Published:First published in Radiation Oncology 7:59
Publisher Policy:Reproduced under a Creative Commons License
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Project CodeAward NoProject NamePrincipal InvestigatorFunder's NameFunder RefLead Dept
563531Overcoming treatment resistance in glioblastoma multiforme by tumour specific inhibition of DNA repairAnthony ChalmersMedical Research Council (MRC)G0802755ICS - PATHOLOGY
563532Overcoming treatment resistance in glioblastoma multiforme by tumour specific inhibition of DNA repairAnthony ChalmersMedical Research Council (MRC)G0802755ICS - PATHOLOGY