Article

A large-scale candidate gene approach identifies SNPs in SOD2 and IL13 as predictive markers of response to preoperative chemoradiation in rectal cancer.

Department of Biology, Val d'Aurelle Cancer Institute, Montpellier, France.
The Pharmacogenomics Journal (impact factor: 4.54). 12/2011; 11(6):437-43. DOI:10.1038/tpj.2010.62 pp.437-43
Source: PubMed

ABSTRACT Neoadjuvant radiochemotherapy followed by total mesorectal excision is now the standard treatment for locally advanced rectal cancer. However, tumor response to chemoradiation varies widely among individuals and cannot be determined before the final pathologic evaluation. The aim of this study was to identify germline genetic markers that could predict sensitivity or resistance to preoperative radiochemotherapy (RT-CT) in rectal cancer. We evaluated the predictive value of 128 single-nucleotide polymorphisms (SNPs) in 71 patients preoperatively treated by RT-CT. The selected SNPs were distributed over 76 genes that are involved in various cellular processes such as DNA repair, apoptosis, proliferation or immune response. The SNPs superoxide dismutase 2 (SOD2) rs4880 (P=0.005) and interleukin-13 (IL13) rs1800925 (P=0.0008) were significantly associated with tumor response to chemoradiation. These results reinforce the idea of using germline polymorphisms for personalized treatment.

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Keywords

128 single-nucleotide polymorphisms
 
apoptosis
 
final pathologic evaluation
 
germline genetic markers
 
germline polymorphisms
 
immune response
 
Neoadjuvant radiochemotherapy
 
preoperative radiochemotherapy
 
rectal cancer
 
SNPs superoxide dismutase 2
 
SOD2
 
standard treatment
 
total mesorectal excision
 
tumor response
 
various cellular processes