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Article Open Access

Association between XRCC1 and ERCC1 single‑nucleotide polymorphisms and the efficacy of concurrent radiochemotherapy in patients with esophageal squamous cell carcinoma

  • Authors:
    • Xue Huang
    • Changmin Liu
    • Yayun Cui
    • Heping Zhang
    • Yongping Liu
    • Xifa Zhou
    • Judong Luo
  • View Affiliations / Copyright

    Affiliations: Department of Radiation Oncology, Changzhou Tumor Hospital Affiliated to Soochow University, Changzhou, Jiangsu 213001, P.R. China, Department of Oncology, Affiliated Hospital of Binzhou Medical College, Binzhou, Shandong 256603, P.R. China, Department of Radiation Oncology, Anhui Provincial Hospital, Hefei, Anhui 230001, P.R. China
    Copyright: © Huang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 704-714
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    Published online on: December 14, 2016
       https://doi.org/10.3892/ol.2016.5496
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Abstract

The aim of the present study was to investigate the association between single‑nucleotide polymorphisms (SNPs) in X‑ray repair cross‑complementing 1‑399 (XRCC1‑399) or excision repair cross‑complementation group 1‑118 (ERCC1‑118) and the short‑term efficacy of radiochemotherapy, tumor metastasis and relapse, as well as the survival time in patients with esophageal squamous cell carcinoma (ESCC). TaqMan probe‑based quantitative polymerase chain reaction (qPCR) was conducted to examine the levels of XRCC1‑399 and ERCC1‑118 SNPs in the peripheral blood of 50 patients with pathologically confirmed ESCC. In addition, the associations between different genotypes and short‑term therapeutic efficacy [the complete remission (CR) rate], tumor metastasis and relapse, as well as the survival time following concurrent radiochemotherapy, were determined. A total of 50 ESCC patients who received concurrent radiochemotherapy were enrolled. It was found that the short‑term therapeutic efficacy (CR rate) was higher in the group of patients carrying the homozygous mutation of XRCC1‑399 (A/A genotype) than in the group of patients without the XRCC1‑399 mutation (G/G genotype). In addition, the CR rate was significantly increased in patients carrying one or two ERCC1‑118 C alleles (C/C or C/T genotype) compared with patients lacking the C allele (T/T genotype). The differences were statistically significant (A/A vs. G/G, P=0.014; TT vs. C/T+C/C, P=0.040). During the follow‑up period, the group of patients carrying the homozygous mutation of XRCC1‑399 (A/A genotype) exhibited a markedly reduced risk of metastasis and relapse compared with the group of patients carrying non‑mutated XRCC1‑399 (G/G genotype; P=0.031). By contrast, ERCC1‑118 SNP was not associated with the risk of metastasis and recurrence (P>0.05). The combined results of univariate and multivariate Cox regression analysis showed that the SNP in ERCC1‑118 was closely associated with survival time. The mean survival time was significantly prolonged in patients carrying 1 or 2 C alleles (C/C or C/T genotype) compared with patients lacking the C allele (T/T genotype) [T/T vs. C/C, HR=12.96, 95% confidence interval (CI)=3.08‑54.61, P<0.001; TT vs. C/T+C/C, HR=11.71, 95% CI=3.06‑44.83, P<0.001]. However, XRCC1‑399SNP had no effect on survival time (P>0.05). XRCCl‑399 SNP was associated with the short‑term therapeutic efficacy (the CR rate) and tumor metastasis/relapse in ESCC patients who received the docetaxel plus cisplatin (TP) regimen‑based concurrent radiochemotherapy. By contrast, ERCC1‑118 SNP was significantly associated with the short‑term therapeutic efficacy (the CR rate) and survival time in ESCC patients who received TP regimen‑based concurrent radiochemotherapy.
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Copy and paste a formatted citation
Spandidos Publications style
Huang X, Liu C, Cui Y, Zhang H, Liu Y, Zhou X and Luo J: Association between XRCC1 and ERCC1 single‑nucleotide polymorphisms and the efficacy of concurrent radiochemotherapy in patients with esophageal squamous cell carcinoma. Oncol Lett 13: 704-714, 2017.
APA
Huang, X., Liu, C., Cui, Y., Zhang, H., Liu, Y., Zhou, X., & Luo, J. (2017). Association between XRCC1 and ERCC1 single‑nucleotide polymorphisms and the efficacy of concurrent radiochemotherapy in patients with esophageal squamous cell carcinoma. Oncology Letters, 13, 704-714. https://doi.org/10.3892/ol.2016.5496
MLA
Huang, X., Liu, C., Cui, Y., Zhang, H., Liu, Y., Zhou, X., Luo, J."Association between XRCC1 and ERCC1 single‑nucleotide polymorphisms and the efficacy of concurrent radiochemotherapy in patients with esophageal squamous cell carcinoma". Oncology Letters 13.2 (2017): 704-714.
Chicago
Huang, X., Liu, C., Cui, Y., Zhang, H., Liu, Y., Zhou, X., Luo, J."Association between XRCC1 and ERCC1 single‑nucleotide polymorphisms and the efficacy of concurrent radiochemotherapy in patients with esophageal squamous cell carcinoma". Oncology Letters 13, no. 2 (2017): 704-714. https://doi.org/10.3892/ol.2016.5496
Copy and paste a formatted citation
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Spandidos Publications style
Huang X, Liu C, Cui Y, Zhang H, Liu Y, Zhou X and Luo J: Association between XRCC1 and ERCC1 single‑nucleotide polymorphisms and the efficacy of concurrent radiochemotherapy in patients with esophageal squamous cell carcinoma. Oncol Lett 13: 704-714, 2017.
APA
Huang, X., Liu, C., Cui, Y., Zhang, H., Liu, Y., Zhou, X., & Luo, J. (2017). Association between XRCC1 and ERCC1 single‑nucleotide polymorphisms and the efficacy of concurrent radiochemotherapy in patients with esophageal squamous cell carcinoma. Oncology Letters, 13, 704-714. https://doi.org/10.3892/ol.2016.5496
MLA
Huang, X., Liu, C., Cui, Y., Zhang, H., Liu, Y., Zhou, X., Luo, J."Association between XRCC1 and ERCC1 single‑nucleotide polymorphisms and the efficacy of concurrent radiochemotherapy in patients with esophageal squamous cell carcinoma". Oncology Letters 13.2 (2017): 704-714.
Chicago
Huang, X., Liu, C., Cui, Y., Zhang, H., Liu, Y., Zhou, X., Luo, J."Association between XRCC1 and ERCC1 single‑nucleotide polymorphisms and the efficacy of concurrent radiochemotherapy in patients with esophageal squamous cell carcinoma". Oncology Letters 13, no. 2 (2017): 704-714. https://doi.org/10.3892/ol.2016.5496
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