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瘦素基因rs2167270 G > A(G19A)多态性可能降低癌症风险:一项涉及19989名受试者的病例对照研究和荟萃分析。

Leptin rs2167270 G > A (G19A) polymorphism may decrease the risk of cancer: A case-control study and meta-analysis involving 19 989 subjects.

作者信息

Yang Jing, Zhong Zhihui, Tang Weifeng, Chen Jianping

机构信息

Department of Gastroenterology, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu, China.

Department of Orthopaedics, Fuzhou Second Hospital Affiliated to Xiamen University, Fuzhou, Fujian, China.

出版信息

J Cell Biochem. 2019 Jul;120(7):10998-11007. doi: 10.1002/jcb.28378. Epub 2019 Jan 29.

Abstract

Accumulating evidence has suggested that leptin (LEP) is very important for the development of cancer. Recently, a number of case-control studies about the relationship of the rs2167270 G > A (G19A) variants in the LEP gene with the risk of cancer have yielded inconsistent results. In this study, we have carried out a case-control study [1063 esophagogastric junction adenocarcinoma (EGJA) cases and 1677 controls] in a Chinese population. Furthermore, we carried out a pooled-analysis of 13 studies involving 8059 cancer patients and 11 930 controls to assess whether the LEP G19A locus was associated with overall cancer susceptibility. Odds ratios (ORs) with the corresponding 95% confidence intervals (CIs) were harnessed to evaluate the potential association. In our case-control study, we found an association between the carriers of LEP 19A allele and EGJA risk. In addition, the results of meta-analysis also suggested significant associations with cancer risk (A vs G: OR = 0.92, 95% CI = 0.88-0.97, P = 0.001; AA vs GG: OR = 0.83, 95% CI = 0.74-0.93, P = 0.001, GA/AA vs GG: OR = 0.93, 95% CI = 0.88-0.99, P = 0.023 and AA vs GG/GA: OR = 0.83, 95% CI = 0.74-0.92, P < 0.001). Upon conducting a stratified analysis, we found that LEP 19A allele might decrease the susceptibility of non-Hodgkin lymphoma (NHL) and colorectal cancer (CRC). In a stratified-by-ethnicity analysis, significant associations were also found in Asians, Caucasians, and mixed populations. We can conclude that the LEP G19A polymorphism constitutes a decreased risk of cancer.

摘要

越来越多的证据表明,瘦素(LEP)对癌症的发展非常重要。最近,一些关于LEP基因中rs2167270 G > A(G19A)变异与癌症风险关系的病例对照研究得出了不一致的结果。在本研究中,我们在中国人群中开展了一项病例对照研究[1063例食管胃交界腺癌(EGJA)病例和1677名对照]。此外,我们对13项涉及8059例癌症患者和11930名对照的研究进行了汇总分析,以评估LEP G19A位点是否与总体癌症易感性相关。利用比值比(OR)及其相应的95%置信区间(CI)来评估潜在关联。在我们的病例对照研究中,我们发现LEP 19A等位基因携带者与EGJA风险之间存在关联。此外,荟萃分析结果还表明与癌症风险存在显著关联(A与G:OR = 0.92,95% CI = 0.88 - 0.97,P = 0.001;AA与GG:OR = 0.83,95% CI = 0.74 - 0.93,P = 0.001,GA/AA与GG:OR = 0.93,95% CI = 0.88 - 0.99,P = 0.023以及AA与GG/GA:OR = 0.83,95% CI = 0.74 - 0.92,P < 0.001)。在进行分层分析时,我们发现LEP 19A等位基因可能会降低非霍奇金淋巴瘤(NHL)和结直肠癌(CRC)的易感性。在按种族分层分析中,在亚洲人、白种人和混合人群中也发现了显著关联。我们可以得出结论:LEP G19A多态性构成了降低的癌症风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3a6/6590124/fe8013e16a56/JCB-120-10998-g003.jpg

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