γ-H2AX level in peripheral blood lymphocytes as a risk predictor for bladder cancer

Mario I. Fernández, Yilei Gong, Yuanqing Ye, Jie Lin, David W. Chang, Ashish M. Kamat, Xifeng Wu

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

Identification of susceptibility to double-strand breaks (DSBs) may provide valuable information about individual bladder cancer (BC) risk. The formation of γ-H2AX foci is a highly sensitive marker for DNA DSBs induction. We assessed whether levels of γ-H2AX in peripheral blood lymphocytes (PBL) obtained after stimulation by ionizing radiation (IR) are able to predict BC risk. Patients were enrolled from an ongoing BC case-control study. Baseline- and IR-induced H2AX phosphorylation was assessed in PBL from 174 newly diagnosed and untreated BC patients and from 174 matched control subjects by a novel, image-based, high-throughput phenotypic assay. The ratio of γ-H2AX level of IR-treated cells to that of non-treated cells (baseline) was used as the parameter to assess the sensitivity to the mutagen. The mean γ-H2AX ratios were significantly higher for cases than for controls (1.43 ± 0.14 versus 1.35 ± 0.12; P = 8.45 × 10-8). This trend was irrespective of age, sex and smoking status. The risk estimates of BC for induced DSBs by tertile distributions in controls showed also a significant trend for increased risk at the highest tertile for the whole cohort (odds ratio = 5.16; 95% confidence interval = 2.69, 9.89; P = 7.78 × 10-7) as well as for each category. Our findings suggest that a higher susceptibility to induction of DSBs as measured by the γ-H2AX assay is significantly associated with an increased risk for BC. This might help to identify individuals at high risk for this cancer, adding new perspectives to established epidemiological and genetic risk factors. Further research of the role of γ-H2AX in biological processes of BC is warranted.

Original languageEnglish (US)
Pages (from-to)2543-2547
Number of pages5
JournalCarcinogenesis
Volume34
Issue number11
DOIs
StatePublished - Nov 2013

ASJC Scopus subject areas

  • Cancer Research

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