| Literature DB >> 30833345 |
Mara Roxana Rubinstein1, Jung Eun Baik1, Stephen M Lagana2, Richard P Han3, William J Raab2, Debashis Sahoo4, Piero Dalerba2,5,6,7, Timothy C Wang6,7, Yiping W Han8,6,7,9.
Abstract
Fusobacterium nucleatum, a Gram-negative oral anaerobe, is a significant contributor to colorectal cancer. Using an in vitro cancer progression model, we discover that F. nucleatum stimulates the growth of colorectal cancer cells without affecting the pre-cancerous adenoma cells. Annexin A1, a previously unrecognized modulator of Wnt/β-catenin signaling, is a key component through which F. nucleatum exerts its stimulatory effect. Annexin A1 is specifically expressed in proliferating colorectal cancer cells and involved in activation of Cyclin D1. Its expression level in colon cancer is a predictor of poor prognosis independent of cancer stage, grade, age, and sex. The FadA adhesin from F. nucleatum up-regulates Annexin A1 expression through E-cadherin. A positive feedback loop between FadA and Annexin A1 is identified in the cancerous cells, absent in the non-cancerous cells. We therefore propose a "two-hit" model in colorectal carcinogenesis, with somatic mutation(s) serving as the first hit, and F. nucleatum as the second hit exacerbating cancer progression after benign cells become cancerous. This model extends the "adenoma-carcinoma" model and identifies microbes such as F. nucleatum as cancer "facilitators".Entities:
Keywords: zzm321990Fusobacterium nucleatumzzm321990; Annexin A1; FadA; colorectal cancer; two‐hit model
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Year: 2019 PMID: 30833345 PMCID: PMC6446206 DOI: 10.15252/embr.201847638
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807