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结直肠癌中 及其受体()单核苷酸多态性的研究:一项涉及2306名受试者的病例对照研究。

Investigation of and its receptor () for single nucleotide polymorphisms in colorectal cancer: a case-control study involving 2,306 subjects.

作者信息

Lin Jing, Xie Zhiqiang, Lan Bin, Guo Zengqing, Tang Wei-Feng, Liu Chao, Zhang Sheng, Chen Gang, Guo Fang, Chen Yu

机构信息

Cancer Bio-immunotherapy Center, Fujian Cancer Hospital & Fujian Medical University Cancer Hospital Fuzhou, Fujian Province, China.

Department of Medical Oncology, Fujian Cancer Hospital & Fujian Medical University Cancer Hospital Fuzhou, Fujian Province, China.

出版信息

Am J Transl Res. 2020 Jul 15;12(7):3613-3628. eCollection 2020.

Abstract

Single nucleotide polymorphisms (SNPs) in the genes coding for leptin () and its receptor () might regulate energy balance and be implicated in the development of colorectal cancer (CRC). In the present investigation, 1,003 CRC cases and 1,303 matched controls was compared. Five functional SNPs in and genes were chosen to evaluate the correlation of these chosen SNPs with CRC susceptibility. We used the SNPscan genotyping assay to genotype and SNPs. A significantly decreased risk of CRC was found to be associated with the rs6588147 polymorphism (GA GG: crude =0.007 and GA/AA GG: crude =0.018). With adjustments for risk factors (e.g. age, gender, drinking, BMI and smoking), these associations were not changed. In subgroup analyses, the association of rs2167270 with a decreased risk of CRC was found in the ≥61 years old subgroup. For rs1137100, the association of this SNP with an increased susceptibility of CRC was found in the BMI <24 kg/m subgroup. In subgroup analyses for rs6588147, we identified that this locus also decreased the susceptibility of CRC in the male subgroup, <61 years old subgroup, never smoking subgroup and never drinking subgroup. For rs1137101, the relationship of this polymorphism with a decreased susceptibility to CRC was found in the never drinking subgroup. In summary, the present study highlights that rs6588147, rs1137101 and rs2167270 may decrease the risk of CRC. However, rs1137100 is associated with susceptibility to CRC. Further case-control studies with larger sample sizes should be conducted to validate our findings.

摘要

编码瘦素()及其受体()的基因中的单核苷酸多态性(SNP)可能调节能量平衡,并与结直肠癌(CRC)的发生有关。在本研究中,对1003例CRC病例和1303例匹配对照进行了比较。选择了和基因中的5个功能性SNP来评估这些选定SNP与CRC易感性的相关性。我们使用SNPscan基因分型检测法对和SNP进行基因分型。发现rs6588147多态性(GA GG:粗比值=0.007,GA/AA GG:粗比值=0.018)与CRC风险显著降低相关。在对风险因素(如年龄、性别、饮酒、BMI和吸烟)进行调整后,这些关联没有改变。在亚组分析中,发现rs2167270与≥61岁亚组中CRC风险降低相关。对于rs1137100,在BMI<24 kg/m亚组中发现该SNP与CRC易感性增加相关。在rs6588147的亚组分析中,我们发现该位点在男性亚组、<61岁亚组、从不吸烟亚组和从不饮酒亚组中也降低了CRC的易感性。对于rs1137101,在从不饮酒亚组中发现该多态性与CRC易感性降低有关。总之,本研究强调rs6588147、rs1137101和rs2167270可能降低CRC风险。然而,rs1137100与CRC易感性相关。应进行更大样本量的进一步病例对照研究以验证我们的发现。

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