慢性炎症が腸幹細胞に長期的影響を残し大腸がんリスクを増加(Chronic inflammation leaves long-lasting impression on gut stem cells, increasing colorectal cancer risk)

ad

2026-03-25 アメリカ国立衛生研究所(NIH)

National Institutes of Healthの研究によると、慢性炎症は腸の幹細胞に長期的な影響を残し、大腸がんリスクを高めることが明らかになった。炎症が収まった後も、腸幹細胞には「記憶」のような変化が残り、遺伝子発現や細胞機能が持続的に変化する。この状態が異常な細胞増殖を促し、がん発生につながる可能性がある。特に炎症により細胞の再生過程が変質し、将来的な腫瘍形成の土台が形成される点が重要とされる。本研究は、炎症とがんの関係を分子レベルで示し、予防や治療戦略の新たな標的を提供する。

<関連情報>

大腸炎のエピジェネティック記憶は腫瘍の増殖を促進する Epigenetic memory of colitis promotes tumour growth

Surya Nagaraja,Lety Ojeda-Miron,Ruochi Zhang,Ena Oreskovic,Conrad Hock,Yan Hu,Daniel Zeve,Karina Sharma,Roni R. Hyman,Qiming Zhang,Andrew Castillo,David T. Breault,Ömer H. Yilmaz & Jason D. Buenrostro
Nature  Published:25 March 2026
DOI:https://doi.org/10.1038/s41586-026-10258-4

慢性炎症が腸幹細胞に長期的影響を残し大腸がんリスクを増加(Chronic inflammation leaves long-lasting impression on gut stem cells, increasing colorectal cancer risk)

Abstract

Chronic inflammation is a well-established risk factor for cancer, but the underlying molecular mechanisms remain unclear1,2. Using a mouse model of colitis, we demonstrate that colonic stem cells retain an epigenetic memory of inflammation following disease resolution that persists for more than 100 days. Here we find that memory of colitis is characterized by a cumulative gain of activator protein 1 (AP-1) transcription factor activity, with durable changes to chromatin accessibility. Further, we develop SHARE-TRACE, a method that enables simultaneous profiling of gene expression, chromatin accessibility and clonal history in single cells, enabling high-resolution tracking of epigenomic memory. This approach reveals that memory of colitis is propagated cell-intrinsically and inherited through stem cell divisions, with some clones demonstrating stronger memory than others. Finally, we show that colitis primes stem cells for increased expression of an AP-1-regulated gene program following oncogenic mutation that accelerates tumour growth, a phenotype dependent on AP-1 activity. Together, our findings provide a mechanistic link between chronic inflammation and malignancy, revealing how long-lived epigenetic alterations in regenerative tissues may contribute to disease susceptibility and suggesting potential diagnostic and therapeutic strategies to mitigate cancer risk in patients with chronic inflammatory conditions.

医療・健康
ad
ad
Follow
ad
タイトルとURLをコピーしました