Wang Yong, Zhang Junfang, Wu Jian, Guan Huaijin
Eye Institute, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Eye Institute, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Exp Mol Pathol. 2017 Apr;102(2):219-223. doi: 10.1016/j.yexmp.2017.02.006. Epub 2017 Feb 12.
The formation and development of age-related cataract (ARC) has been demonstrated to have the involvement of defective DNA repair in lens epithelial cells (LECs). This study aimed to investigate DNA repair genes expression in human lens cortex collected from age-related cortical cataract (ARCC) and controls during surgery. The expression levels of the genes were evaluated by xx genes microarray analysis. The results were further confirmed by Quantitative Real-Time PCR (qRT-PCR). The mRNA levels of 7 genes decreased and 4 genes out of 92 genes increased in lens cortex of ARCCs compared with controls with the fold change >1.5. Using Comet assay, we found the DNA breaks in the LECs of ARCCs were obviously severer than that of controls. The present data provide a global perspective on expression of DNA repair genes that may contribute to cataract pathogenesis. The DNA damage and repair pathway might be an effective target to delay the onset of ARC.
年龄相关性白内障(ARC)的形成和发展已被证明与晶状体上皮细胞(LEC)中DNA修复缺陷有关。本研究旨在调查手术期间从年龄相关性皮质性白内障(ARCC)和对照组收集的人晶状体皮质中DNA修复基因的表达情况。通过xx基因微阵列分析评估基因的表达水平。结果通过定量实时PCR(qRT-PCR)进一步证实。与对照组相比,ARCCs晶状体皮质中7个基因的mRNA水平下降,92个基因中有4个基因增加,变化倍数>1.5。使用彗星试验,我们发现ARCCs的LECs中的DNA断裂明显比对照组严重。目前的数据提供了关于可能导致白内障发病机制的DNA修复基因表达的全面观点。DNA损伤和修复途径可能是延缓ARC发病的有效靶点。