[Urine proteomics signatures associated with alcohol drinking among residents attending the National Upper Gastrointestinal Cancer Early Detection Program in Linqu, Shandong province]

Zhonghua Yu Fang Yi Xue Za Zhi. 2021 Sep 6;55(9):1139-1144. doi: 10.3760/cma.j.cn112150-20210312-00247.
[Article in Chinese]

Abstract

The liquid chromatography tandem mass spectrometry was used to detect the urinary proteomics of 223 residents aged 40-69 years old who participated in the National Upper Gastrointestinal Cancer Early Detection Program in Linqu County, Shandong Province from November 22 to December 7, 2018, and analyze the alcohol consumption related proteomic profiles and individual urinary protein. There were significant differences in urinary protein profiles between alcohol consumption group and non-alcohol consumption group. The expression of 26 urinary proteins was up-regulated and 20 urinary proteins were down-regulated in alcohol consumption group (P<0.05). The differentially expressed proteins had enzyme inhibitor activity and phospholipid binding function, and mainly enriched in pathways involving proximal tubule bicarbonate regeneration, complement and coagulation cascade, and cholesterol metabolism. The protein expressions of complement factor I (CFI), angiotensin converting enzyme 2 (ACE2) and protein C inhibitor (SERPINA5) were positively correlated with daily alcohol consumption.

采用液相色谱串联质谱,对山东省临朐县于2018年11月22日—12月7日期间参与国家上消化道癌早诊早治项目的223名40~69岁居民进行尿蛋白质组学检测,分析饮酒相关蛋白质组学图谱和个体尿蛋白。饮酒组与不饮酒组的尿蛋白质图谱有明显差异,饮酒组中有26个尿蛋白表达上调,20个尿蛋白表达下调(P值均<0.05)。差异蛋白具有酶抑制剂活性和磷脂结合功能,富集于近端小管碳酸氢盐再生、凝血与补体级联和胆固醇代谢等通路。补体因子I(CFI)、血管紧张素转换酶2(ACE2)和蛋白C抑制剂(SERPINA5)的蛋白表达量与每日饮酒量呈正相关。.

MeSH terms

  • Adult
  • Aged
  • Alcohol Drinking
  • Chromatography, Liquid
  • Early Detection of Cancer
  • Gastrointestinal Neoplasms*
  • Humans
  • Middle Aged
  • Proteomics*