Association of cigarette smoking with risk of colorectal cancer subtypes classified by gut microbiota

被引:2
作者
Cai, Jia-An [1 ]
Zhang, Yong-Zhen [2 ,3 ]
Yu, En-Da [4 ]
Ding, Wei-Qun [1 ]
Li, Zhao-Shen [2 ,5 ]
Zhong, Liang [1 ,6 ]
Cai, Quan-Cai [2 ,5 ]
机构
[1] Fudan Univ, Huashan Hosp, Dept Gastroenterol & Endoscopy, Shanghai, Peoples R China
[2] Naval Med Univ, Changhai Hosp, Dept Gastroenterol, Shanghai, Peoples R China
[3] 928 Hosp PLA Joint Logist Force, Dept Gastroenterol, Haikou, Peoples R China
[4] Naval Med Univ, Changhai Hosp, Dept Gen Surg, Shanghai, Peoples R China
[5] Natl Clin Res Ctr Digest Dis, Shanghai, Peoples R China
[6] Fudan Univ, Huashan Hosp, Dept Gastroenterol & Endoscopy, 12 Middle Wulumuqi Rd, Shanghai 200040, Peoples R China
基金
中国国家自然科学基金;
关键词
colorectal cancer cigarette; smoking case-control study; gut microbiota; OPPORTUNITIES;
D O I
10.18332/tid/168515
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
INTRODUCTION Both cigarette smoking and gut microbiota play important roles in colorectal carcinogenesis. We explored whether the association between smoking and colorectal cancer (CRC) risk varies by gut microbial enterotypes and how smoking-related enterotypes promote colorectal carcinogenesis. METHODS A case-control study was conducted. Fecal microbiota was determined by 16S rDNA sequencing. The cases with CRC or adenoma were subclassified by gut microbiota enterotypes. Multivariate analyses were used to test associations between smoking and the odds of colorectal neoplasm subtypes. Mann-Whitney U tests were used to find differential genera, genes, and pathways between the subtypes. RESULTS Included in the study were 130 CRC patients (type I: n=77; type II: n=53), 120 adenoma patients (type I: n=66; type II: n=54), and 130 healthy participants. Smoking increased the odds for type II tumors significantly (all p for trend <0.05) but not for type I tumors. The associations of smoking with increased odds of colorectal neoplasm significantly differed by gut microbiota enterotypes (p<0.05 for heterogeneity). An increase in carcinogenic bacteria (genus Escherichia shigella) and a decrease in probiotics (family Lachnospiraceae and Ruminococcaceae) in type II tumors may drive disease progression by upregulating oncogenic signaling pathways and inflammatory/oxidative stress response pathways, as well as protein phospholipase D1/2, cytochrome C, and prostaglandin-endoperoxide synthase 2 expression. CONCLUSIONS Smoking was associated with a higher odds of type II colorectal neoplasms but not type I tumors, supporting a potential role for the gut microbiota in mediating the association between smoking and colorectal neoplasms.
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页数:14
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