Abstract

BackgroundX-ray repair cross-complementing group 1 (XRCC1) protein plays an important role in the repair of DNA damage and adducts. Single nucleotide polymorphisms (SNPs) of XRCC1 are suspected to have some relationship with response to chemotherapy and overall survival of lung cancer. This meta-analysis aimed to summarize published data on the association between the commonest SNPs of XRCC1 (Arg194Trp, C > T, rs1799782 and Arg399Gln, G > A, rs25487) and clinical outcome of lung cancer patients.MethodsWe retrieved the relevant articles from PubMed, EMBASE and the China National Knowledge Infrastructure (CNKI) databases. Studies were selected using specific inclusion and exclusion criteria. Primary outcomes included objective response (i.e., complete response + partial response vs. progressive disease + stable disease) and overall survival (OS). Odds ratio (OR) or hazard ratio (HR) with 95% confidence interval (CI) were estimated. All analyses were performed using the Stata software.ResultsTwenty-two articles were included in the present analysis. XRCC1 Arg194Trp and Arg399Gln polymorphisms were significantly associated with response to treatment in lung cancer patients. Patients with C/T genotype, T/T genotype and minor variant T allele at Arg194Trp were more likely to respond to platinum-based chemotherapy compared with those with C/C genotype (C/T vs. C/C: OR, 2.54; 95%CI, 1.95-3.31; T/T vs. C/C: OR, 2.06; 95%CI, 1.39-3.06; C/T+T/T vs. C/C: OR, 2.42; 95% CI, 1.88-3.10). For XRCC1 Arg399Gln, G/A genotype, A/A genotype and minor variant A allele were associated with objective response in all patients (G/A vs. G/G: OR, 0.67; 95%CI, 0.50-0.90; A/A vs. G/G: OR, 0.43; 95%CI, 0.25-0.73; A/A+G/A vs. G/G: OR, 0.63; 95%CI, 0.49-0.83). Both G/A and A/A genotypes of XRCC1 Arg399Gln could influence overall survival of lung cancer patients (G/A vs. G/G: HR, 1.23; 95%CI, 1.06-1.44; A/A vs. G/G: HR, 2.03; 95%CI, 1.20-3.45). Interaction analysis suggested that compared with the patients carrying C/T+T/T genotype at XRCC1 194 and G/G genotype at XRCC1 399, the patients carrying 194 C/C and 399 G/A+A/A or 194 C/C and 399 G/G genotype showed much worse objective response.ConclusionsGenetic polymorphisms in XRCC1 gene might be associated with overall survival and response to platinum-based chemotherapy in lung cancer patients.

Highlights

  • X-ray repair cross-complementing group 1 (XRCC1) protein plays an important role in the repair of DNA damage and adducts

  • X-ray repair cross-complementing group 1 (XRCC1) protein plays a central role in base excision repair (BER) pathway by interacting with other DNA repair proteins, giving the possibility that XRCC1 has some relationship with the response to therapy and the overall survival of lung cancer

  • XRCC1 Arg194Trp Since the study on the association between XRCC1 Arg194Trp polymorphism with PFS or overall survival (OS) was too few to be applied in the present meta-analysis, we only analyzed the association of XRCC1 Arg194Trp polymorphism and objective response in lung cancer patients

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Summary

Introduction

X-ray repair cross-complementing group 1 (XRCC1) protein plays an important role in the repair of DNA damage and adducts. Single nucleotide polymorphisms (SNPs) of XRCC1 are suspected to have some relationship with response to chemotherapy and overall survival of lung cancer. There are some molecular markers showing potential as therapeutic and prognostic indicators, but none could be used into clinical practice [5,6] In these factors, DNA repair capacity (DRC) is an important one. It has been speculated that single nucleotide polymorphisms (SNPs) in DNA repair genes may change gene expression and activity, influence the effectiveness of cancer treatment and survival of patients [8]. X-ray repair cross-complementing group 1 (XRCC1) protein plays a central role in base excision repair (BER) pathway by interacting with other DNA repair proteins, giving the possibility that XRCC1 has some relationship with the response to therapy and the overall survival of lung cancer

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