Evaluating the role of mitochondrial DNA variation to the genetic predisposition to radiation-induced toxicity

被引:10
作者
Fachal, Laura [1 ]
Mosquera-Miguel, Ana [2 ,3 ]
Gomez-Caamano, Antonio [4 ]
Sanchez-Garcia, Manuel [5 ]
Calvo, Patricia [4 ]
Lobato-Busto, Ramon [5 ]
Salas, Antonio [2 ,3 ]
Vega, Ana [1 ]
机构
[1] Fdn Publ Galega Med Xen SERGAS, Grp Med Xen, CIBERER, IDIS, Santiago De Compostela, Spain
[2] Univ Santiago de Compostela, Fac Med, Inst Ciencias Forenses, Unidade Xenet, Galicia, Spain
[3] Univ Santiago de Compostela, Fac Med, Dept Anat Patol & Ciencias Forenses, Galicia, Spain
[4] Complexo Hosp Univ Santiago, SERGAS, Dept Radiat Oncol, Santiago De Compostela, Spain
[5] Complex Hosp Univ Santiago, SERGAS, Dept Med Phys, Santiago De Compostela, Spain
关键词
Prostate cancer; 3D-CRT; SNP; mtDNA; PROSTATE-CANCER PATIENTS; HAPLOGROUPS; RISK; APOPTOSIS; SEQUENCE; DISEASE; GENOME;
D O I
10.1016/j.radonc.2014.03.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and purpose: Mitochondrial DNA common variants have been reported to be associated with the development of radiation-induced toxicity. Using a large cohort of patients, we aimed to validate these findings by investigating the potential role of common European mitochondrial DNA SNPs (mtSNPs) to the development of radio-toxicity. Material and methods: Overall acute and late toxicity data were assessed in a cohort of 606 prostate cancer patients by means of Standardized Total Average Toxicity (STAT) score. We carried out association tests between radiation toxicity and a selection of 15 mtSNPs (and the haplogroups defined by them). Results: Statistically significant association between mtSNPs and haplogroups with toxicity could not be validated in our Spanish cohort. Conclusions: The present study suggests that the mtDNA common variants analyzed are not associated with clinically relevant increases in risk of overall radiation-induced toxicity in prostate cancer patients. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:199 / 205
页数:7
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