Yu Zhi-Hong, Chen Miao, Zhang Qing-Qian, Hu Xun
Department of Oncology, Tongde Hospital of Zhejiang Province, Hangzhou, China.
Department of Thoracic Surgery, The Second Hospital of Jiaxing, Jiaxing, China.
Comb Chem High Throughput Screen. 2018;21(10):704-710. doi: 10.2174/1386207322666190125150557.
The association between vitamin D receptor (VDR) genetic polymorphism and lung cancer risk has been evaluated by the previous meta-analyses. Due to the emergence of novel studies and inappropriate inclusion of overlapping populations, an updated meta-analysis on recent evidences is necessarily needed. We comprehensively searched databases of PubMed, Web of Science and Chinese National Knowledge Infrastructure and finally obtained 7 eligible studies according to the inclusion criteria. Four positions on VDR gene, namely ApaI (rs7975232), BsmI (rs1544410), FokI (rs10735810) and TaqI (rs731236), were considered in this investigation. Data pooling found no significant association of lung cancer risk with ApaI or FokI. In contrast, it was indicated that the BsmI A allele was negatively related to the lung cancer risk, compared with the G allele (OR = 0.51, 95% CI = 0.33-0.79). Individuals with BsmI AA (OR = 0.53, 95% CI = 0.26-1.11) and AG genotypes (OR = 0.46, 95% CI = 0.30-0.71) showed decreased risk of lung cancer, compared with those of GG genotype. Regarding the TaqI polymorphism, the T allele carriers were at increased risk of lung cancer (OR = 1.25, 95% CI = 1.04-1.50). Compared with the TaqI TC+CC genotype, the TT genotype was positively associated with lung cancer risk (OR = 1.42, 95% CI = 1.11-1.82). No publication bias was identified in any of the analysis. In conclusion, VDR genetic polymorphism may be correlated to lung cancer risk. Given limited number of the included studies, more observations are warranted to draw a safer conclusion.
先前的荟萃分析已对维生素D受体(VDR)基因多态性与肺癌风险之间的关联进行了评估。由于新研究的出现以及对重叠人群的不适当纳入,有必要对近期证据进行更新的荟萃分析。我们全面检索了PubMed、Web of Science和中国知网数据库,最终根据纳入标准获得了7项符合条件的研究。本研究考虑了VDR基因上的四个位点,即ApaI(rs7975232)、BsmI(rs1544410)、FokI(rs10735810)和TaqI(rs731236)。数据合并发现肺癌风险与ApaI或FokI无显著关联。相比之下,研究表明,与G等位基因相比,BsmI A等位基因与肺癌风险呈负相关(OR = 0.51,95% CI = 0.33 - 0.79)。与GG基因型个体相比,BsmI AA(OR = 0.53,95% CI = 0.26 - 1.11)和AG基因型个体(OR = 0.46,95% CI = 0.30 - 0.71)患肺癌的风险降低。关于TaqI多态性,T等位基因携带者患肺癌的风险增加(OR = 1.25,95% CI = 1.04 - 1.50)。与TaqI TC + CC基因型相比,TT基因型与肺癌风险呈正相关(OR = 1.42,95% CI = 1.11 - 1.82)。在任何分析中均未发现发表偏倚。总之,VDR基因多态性可能与肺癌风险相关。鉴于纳入研究数量有限,需要更多观察以得出更可靠的结论。