MRE11 and ATM Expression Levels Predict Rectal Cancer Survival and Their Association with Radiotherapy Response

PLoS One. 2016 Dec 8;11(12):e0167675. doi: 10.1371/journal.pone.0167675. eCollection 2016.

Abstract

Background: Aberrant expression of DNA repair proteins is associated with poor survival in cancer patients. We investigated the combined expression of MRE11 and ATM as a predictive marker of response to radiotherapy in rectal cancer.

Methods: MRE11 and ATM expression were examined in tumor samples from 262 rectal cancer patients who underwent surgery for rectal cancer, including a sub-cohort of 54 patients who were treated with neoadjuvant radiotherapy. The relationship between expression of the two-protein panel and tumor regression grade (TRG) was assessed by Mann-Whitney U test and receiver operating characteristics area under curve (ROC-AUC) analysis. The association between expression of the two-protein panel and clinicopathologic variables and survival was examined by Kaplan-Meier methods and Cox regression analysis.

Results: A high score for two-protein combined expression in the tumor center (TC) was significantly associated with worse disease-free survival (DFS) (P = 0.035) and overall survival (OS) (P = 0.003) in the whole cohort, and with DFS (P = 0.028) and OS (P = 0.024) in the neoadjuvant subgroup (n = 54). In multivariate analysis, the two-protein combination panel (HR = 2.178, 95% CI 1.115-4.256, P = 0.023) and perineural invasion (HR = 2.183, 95% CI 1.222-3.899, P = 0.008) were significantly associated with DFS. Using ROC-AUC analysis of good versus poor histological tumor response among patients treated preoperatively with radiotherapy, the average ROC-AUC was 0.745 for the combined panel, 0.618 for ATM alone, and 0.711 for MRE11 alone.

Conclusions: The MRE11/ATM two-protein panel developed in this study may have clinical value as a predictive marker of tumor response to neoadjuvant radiotherapy, and a prognostic marker for disease-free and overall survival.

MeSH terms

  • Aged
  • Ataxia Telangiectasia Mutated Proteins / metabolism*
  • DNA-Binding Proteins / metabolism*
  • Female
  • Humans
  • MRE11 Homologue Protein
  • Male
  • Prognosis
  • ROC Curve
  • Rectal Neoplasms / pathology*
  • Rectal Neoplasms / radiotherapy
  • Survival Analysis

Substances

  • DNA-Binding Proteins
  • MRE11 protein, human
  • ATM protein, human
  • Ataxia Telangiectasia Mutated Proteins
  • MRE11 Homologue Protein

Grants and funding

We would like to declare that funding support for this research was in part contributed through the Cancer Institute of NSW grant awarded to Professor Paul DeSouza and Professor C Soon Lee (Center for Oncology Education and Research Translation) Award number: 13/TRC/1-01.