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Tytuł pozycji:

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

Tytuł:
γ-H2AX level in peripheral blood lymphocytes as a risk predictor for bladder cancer.
Autorzy:
Fernández MI; Department of Urology and.
Gong Y
Ye Y
Lin J
Chang DW
Kamat AM
Wu X
Źródło:
Carcinogenesis [Carcinogenesis] 2013 Nov; Vol. 34 (11), pp. 2543-7. Date of Electronic Publication: 2013 Aug 14.
Typ publikacji:
Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Publication: Oxford : Irl Press At Oxford University Press
Original Publication: [New York, IRL Press]
MeSH Terms:
Biomarkers, Tumor/*blood
Gamma Rays/*adverse effects
Histones/*blood
Lymphocytes/*metabolism
Urinary Bladder Neoplasms/*blood
Aged ; Case-Control Studies ; DNA Damage ; DNA Repair ; Female ; Follow-Up Studies ; Humans ; Lymphocytes/radiation effects ; Male ; Odds Ratio ; Phosphorylation ; Prognosis ; Urinary Bladder Neoplasms/diagnosis ; Urinary Bladder Neoplasms/etiology
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Grant Information:
P50 CA 91846 United States CA NCI NIH HHS; R01 CA 74880 United States CA NCI NIH HHS; U01 CA 127615 United States CA NCI NIH HHS
Substance Nomenclature:
0 (Biomarkers, Tumor)
0 (H2AX protein, human)
0 (Histones)
Entry Date(s):
Date Created: 20130816 Date Completed: 20140122 Latest Revision: 20211021
Update Code:
20240104
PubMed Central ID:
PMC3810842
DOI:
10.1093/carcin/bgt270
PMID:
23946494
Czasopismo naukowe
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.

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