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Article: An interplay between human genetics and intratumoral microbiota in the progression of colorectal cancer
| Title | An interplay between human genetics and intratumoral microbiota in the progression of colorectal cancer |
|---|---|
| Authors | |
| Issue Date | 29-Apr-2025 |
| Publisher | Cell Press |
| Citation | Cell Host & Microbe, 2025 How to Cite? |
| Abstract | Intratumoral microbiota plays a crucial role in cancer progression. However, the relationship between host genetics and intratumoral microbiota, as well as their interaction in colorectal cancer (CRC) progression, remains unclear. With 748 Chinese CRC patients enrolled from three cohorts, we find that the single nucleotide polymorphism (SNP) rs2355016, located in the intron of ATP-sensitive inward rectifier potassium channel 11 (KCNJ11), is significantly associated with the abundance of Fusobacterium. Compared with the rs2355016 GG genotype, patients carrying the A allele exhibit downregulation of KCNJ11 and enrichment of Fusobacterium, which corresponds to accelerated proliferation and progression. Low expression of KCNJ11 can increase the level of galactose-N-acetyl-d-galactosamine (Gal-GalNAc) on the surface of CRC cells, thereby facilitating the binding of the Fap2 protein from F. nucleatum to Gal-GalNAc. This further enhances the adhesion and invasion of F. nucleatum and promotes CRC growth. Our study explores the interaction between intratumoral microbiota and SNPs in CRC patients, which will enhance our understanding of CRC proliferation. |
| Persistent Identifier | http://hdl.handle.net/10722/355779 |
| ISSN | 2023 Impact Factor: 20.6 2023 SCImago Journal Rankings: 7.760 |
| ISI Accession Number ID |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Yu, Jing | - |
| dc.contributor.author | Liang, Yuxuan | - |
| dc.contributor.author | Zhang, Qingrong | - |
| dc.contributor.author | Ding, Hui | - |
| dc.contributor.author | Xie, Minghao | - |
| dc.contributor.author | Zhang Jingjing | - |
| dc.contributor.author | Hu, Wenyan | - |
| dc.contributor.author | Xu, Sihua | - |
| dc.contributor.author | Xiao, Yiyuan | - |
| dc.contributor.author | Xu, Sha | - |
| dc.contributor.author | Na, Rong | - |
| dc.contributor.author | Wu, Baixing | - |
| dc.contributor.author | Zhou, Jiaming Zhou | - |
| dc.contributor.author | Chen, Haitao | - |
| dc.date.accessioned | 2025-05-13T00:35:21Z | - |
| dc.date.available | 2025-05-13T00:35:21Z | - |
| dc.date.issued | 2025-04-29 | - |
| dc.identifier.citation | Cell Host & Microbe, 2025 | - |
| dc.identifier.issn | 1931-3128 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/355779 | - |
| dc.description.abstract | <p>Intratumoral microbiota plays a crucial role in cancer progression. However, the relationship between host genetics and intratumoral microbiota, as well as their interaction in colorectal cancer (CRC) progression, remains unclear. With 748 Chinese CRC patients enrolled from three cohorts, we find that the single nucleotide polymorphism (SNP) rs2355016, located in the intron of ATP-sensitive inward rectifier potassium channel 11 (KCNJ11), is significantly associated with the abundance of Fusobacterium. Compared with the rs2355016 GG genotype, patients carrying the A allele exhibit downregulation of KCNJ11 and enrichment of Fusobacterium, which corresponds to accelerated proliferation and progression. Low expression of KCNJ11 can increase the level of galactose-N-acetyl-d-galactosamine (Gal-GalNAc) on the surface of CRC cells, thereby facilitating the binding of the Fap2 protein from F. nucleatum to Gal-GalNAc. This further enhances the adhesion and invasion of F. nucleatum and promotes CRC growth. Our study explores the interaction between intratumoral microbiota and SNPs in CRC patients, which will enhance our understanding of CRC proliferation.<br></p> | - |
| dc.language | eng | - |
| dc.publisher | Cell Press | - |
| dc.relation.ispartof | Cell Host & Microbe | - |
| dc.title | An interplay between human genetics and intratumoral microbiota in the progression of colorectal cancer | - |
| dc.type | Article | - |
| dc.identifier.doi | 10.1016/j.chom.2025.04.003 | - |
| dc.identifier.eissn | 1934-6069 | - |
| dc.identifier.isi | WOS:001501666000001 | - |
| dc.identifier.issnl | 1931-3128 | - |
