Rakmanee Sarinthorn, Pakakasama Samart, Hongeng Suradej, Sanguansin Sirima, Thongmee Acharawan, Pongstaporn Wanida
Department of Biomedical Science, 4Microbiology unit, Department of Biomedical Science, Faculty of Science, Rangsit University, Pathumthani, Thailand. Email:
Asian Pac J Cancer Prev. 2017 Apr 1;18(4):1117-1120. doi: 10.22034/APJCP.2017.18.4.1117.
Objectives: This study assessed associations of the miR196a2 (rs11614913) T>C polymorphism withsusceptibility to childhood acute lymphoblastic leukemia (ALL) and clinical outcomes. Materials and Methods: Blood DNA samples from 104 childhood ALL patients and 180 healthy children were studied for the miR-196a2 (rs11614913) polymorphism using a polymerase chain reaction-restriction fragment-length polymorphism (PCR-RFLP) approach. Results: The frequency of the miR-196a2 (rs11614913) T allele in controls was 0.51 compared with 0.33 in ALL cases. In this study, CC, TC heterozygote and CC/TC genotypes were significantly associated with increase childhood ALL susceptibility compared with the TT wild type (OR =4.321, 95% CI = 2.091-8.930 p=0.000, OR = 2.248, 95% CI =1.103-4.579, p=0.024, OR = 2.921, 95% CI = 1.504-5.673 p=0.001, respectively). However, the miR-196a2 (rs11614913) T>C polymorphism was not associated with demographic data or clinico-pathological data in ALL cases. Conclusion: CC, TC and CC+TC genotypes of miR-196a2 (rs11614913) was significantly associated with increased susceptibility in Thai childhood ALL but not with clinical variables.
本研究评估了miR196a2(rs11614913)T>C多态性与儿童急性淋巴细胞白血病(ALL)易感性及临床结局之间的关联。材料与方法:采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,对104例儿童ALL患者和180例健康儿童的血液DNA样本进行miR-196a2(rs11614913)多态性研究。结果:对照组中miR-196a2(rs11614913)T等位基因频率为0.51,而ALL病例组为0.33。在本研究中,与TT野生型相比,CC、TC杂合子和CC/TC基因型与儿童ALL易感性增加显著相关(OR = 4.321,95%CI = 2.091 - 8.930,p = 0.000;OR = 2.248,95%CI = 1.103 - 4.579,p = 0.024;OR = 2.921,95%CI = 1.504 - 5.673,p = 0.001)。然而,miR-196a2(rs11614913)T>C多态性与ALL病例的人口统计学数据或临床病理数据无关。结论:miR-196a2(rs11614913)的CC、TC和CC + TC基因型与泰国儿童ALL易感性增加显著相关,但与临床变量无关。