Possible Role of the WDR3 Gene on Genome Stability in Thyroid Cancer Patients
Author(s) -
Wilser Andrés García-Quispes,
Susana Pastor,
Pere Galofré,
Josefina Biarnés,
Joan Martí i Castell,
Antonia Velázquez,
Ricard Marcos
Publication year - 2012
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0044288
Subject(s) - genome instability , thyroid cancer , binucleated cells , micronucleus , micronucleus test , single nucleotide polymorphism , genotype , biology , gene , microbiology and biotechnology , genetics , dna damage , genome , peripheral blood , ionizing radiation , irradiation , cancer , medicine , dna , immunology , physics , toxicity , nuclear physics
The role of the WDR3 gene on genomic instability has been evaluated in a group of 115 differentiated thyroid cancer (DTC) patients. Genomic instability has been measured according to the response of peripheral blood lymphocytes to ionizing radiation (0.5 Gy). The response has been measured with the micronucleus (MN) test evaluating the frequency of binucleated cells with MN (BNMN), both before and after the irradiation. No differences between genotypes, for the BNMN frequencies previous the irradiation, were observed. Nevertheless significant decreases in DNA damage after irradiation were observed in individuals carrying the variant alleles for each of the three genotyped SNPs: rs3754127 [−8.85 (−15.01 to −2.70), P<0.01]; rs3765501 [−8.98 (−15.61 to −2.36), P<0.01]; rs4658973 [−8.70 (−14.94 to −2.46), P<0.01]. These values correspond to those obtained assuming a dominant model. This study shows for the first time that WDR3 can modulate genome stability.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom