Li Ning, Luo Huaichao, Liu Xiaoqi, Ma Shi, Lin He, Chen Rong, Hao Fang, Zhang Dingding
Sichuan Provincial Key Laboratory for Human Disease Gene Study, the Institute of Laboratory Medicine, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, Chengdu, Sichuan, China.
Department of Immunology, Zunyi Medical College, Zunyi, Guizhou, China.
Oncotarget. 2016 Jan 5;7(1):23-32. doi: 10.18632/oncotarget.6627.
FOXO3, AKT1 and IGF-2R are critical members of the insulin/IGF-1 signaling pathway. Previous studies showed that polymorphisms (SNPs) in FOXO3, AKT1 and IGF-2R were associated with human longevity in Caucasian population. However, the association of these SNPs in different ethnic groups is often inconsistent. Here, we investigated the association of genetic variants in three genes with human longevity in Han Chinese population. Twelve SNPs from FOXO3, AKT1 and IGF-2R were selected and genotyped in 1202 long-lived individuals (nonagenarians and centenarians) and younger individuals. Rs9486902 of FOXO3 was found to be associated with human longevity in both genders combined in this study (allelic P = 0.002, corrected P = 0.024). The other eleven SNPs were not significantly associated with human longevity in Han Chinese population. The haplotypes TTCTT, CCTTC and CTCCT of FOXO3 as well as GGTCGG and GGTCAG of AKT1 were shown to have a significant difference between case and control (P =0.006, 2.78×10-5, 4.68×10-6, 0.003,0.005, respectively). The estimated prevalence of diabetes and prediabetes in long-lived individuals was significantly lower than in common adult populations (P = 0.001, 2.3×10-26) .Therefore, the search for longevity-associated genes provides the identification of new potential targets beneficial for the treatment of diabetes.
FOXO3、AKT1和IGF-2R是胰岛素/IGF-1信号通路的关键成员。先前的研究表明,FOXO3、AKT1和IGF-2R中的多态性(单核苷酸多态性)与高加索人群的人类长寿有关。然而,这些单核苷酸多态性在不同种族群体中的关联往往不一致。在此,我们调查了这三个基因中的遗传变异与汉族人群人类长寿的关联。从FOXO3、AKT1和IGF-2R中选择了12个单核苷酸多态性,并在1202名长寿个体(九旬老人和百岁老人)和年轻个体中进行基因分型。在本研究中,发现FOXO3的Rs9486902与男女合并的人类长寿有关(等位基因P = 0.002,校正P = 0.024)。其他11个单核苷酸多态性与汉族人群的人类长寿无显著关联。FOXO3的单倍型TTCTT、CCTTC和CTCCT以及AKT1的GGTCGG和GGTCAG在病例组和对照组之间显示出显著差异(P分别为0.006、2.78×10-5、4.68×10-6、0.003、0.005)。长寿个体中糖尿病和糖尿病前期的估计患病率显著低于普通成年人群(P = 0.001,2.3×10-26)。因此,寻找与长寿相关的基因有助于识别对糖尿病治疗有益的新潜在靶点。