Contribution of pks plus Escherichia coli (E. coli) to Colon Carcinogenesis

被引:6
|
作者
Sadeghi, Mohammad [1 ]
Mestivier, Denis [1 ]
Sobhani, Iradj [1 ,2 ]
机构
[1] Paris East Creteil Univ UPEC, EA7375 EC2M3 Early, Detect Colon Canc Using Microbial & Mol Markers, F-94010 Creteil, France
[2] Henri Mondor Hosp, APHP, Dept Gastroenterol, F-94010 Creteil, France
基金
美国国家卫生研究院;
关键词
pks plus E. coli; colorectal cancer; colon; gut microbiota; diagnosis; therapy; CYTOLETHAL DISTENDING TOXIN; CYTOTOXIC NECROTIZING FACTOR-1; ASSEMBLY-LINE ENZYMOLOGY; PERSISTENT DNA-DAMAGE; CELL-CYCLE; NONRIBOSOMAL PEPTIDE; COLORECTAL-CANCER; COLIBACTIN BIOSYNTHESIS; INTESTINAL INFLAMMATION; BACTERIAL GENOTOXIN;
D O I
10.3390/microorganisms12061111
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Colorectal cancer (CRC) stands as a significant global health concern, ranking second in mortality and third in frequency among cancers worldwide. While only a small fraction of CRC cases can be attributed to inherited genetic mutations, the majority arise sporadically due to somatic mutations. Emerging evidence reveals gut microbiota dysbiosis to be a contributing factor, wherein polyketide synthase-positive Escherichia coli (pks+ E. coli) plays a pivotal role in CRC pathogenesis. pks+ bacteria produce colibactin, a genotoxic protein that causes deleterious effects on DNA within host colonocytes. In this review, we examine the role of the gut microbiota in colon carcinogenesis, elucidating how colibactin-producer bacteria induce DNA damage, promote genomic instability, disrupt the gut epithelial barrier, induce mucosal inflammation, modulate host immune responses, and influence cell cycle dynamics. Collectively, these actions foster a microenvironment conducive to tumor initiation and progression. Understanding the mechanisms underlying pks+ bacteria-mediated CRC development may pave the way for mass screening, early detection of tumors, and therapeutic strategies such as microbiota modulation, bacteria-targeted therapy, checkpoint inhibition of colibactin production and immunomodulatory pathways.
引用
收藏
页数:23
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