Inflammatory bowel disease, colitis, and cancer: unmasking the chronic inflammation link

被引:4
|
作者
Shahgoli, Vahid Khaze [1 ,2 ]
Noorolyai, Saeed [1 ]
Ahmadpour Youshanlui, Mahya [1 ]
Saeidi, Hossein [1 ]
Nasiri, Hadi [1 ]
Mansoori, Behzad [3 ]
Holmskov, Uffe [2 ]
Baradaran, Behzad [1 ]
机构
[1] Tabriz Univ Med Sci, Immunol Res Ctr, Fac Med, Immunol, Tabriz, Iran
[2] Univ Southern Denmark, Dept Mol Med, Odense, Denmark
[3] Wistar Inst Anat & Biol, Mol & Cellular Oncogenesis Program, Philadelphia, PA USA
关键词
Chronic inflammation; Colitis-associated colorectal cancer; Inflammatory bowel diseases; Pro-inflammatory mediators; SUICIDE GENE-THERAPY; NF-KAPPA-B; COLORECTAL-CANCER; SIGNALING PATHWAY; CLINICAL DEVELOPMENT; ULCERATIVE-COLITIS; SUPPRESSOR-CELLS; BIOLOGIC THERAPY; IMMUNE CELLS; MECHANISMS;
D O I
10.1007/s00384-024-04748-y
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BackgroundChronic inflammation is a significant driver in the development of various diseases, including cancer. Colitis-associated colorectal cancer (CA-CRC) refers to the increased risk of colorectal cancer in individuals with chronic inflammatory bowel diseases (IBD) such as ulcerative colitis and Crohn's disease.MethodsThis narrative review examines the link between chronic inflammation and CA-CRC. A comprehensive literature search was conducted using PubMed, Scopus, and Web of Science, focusing on studies published between 2000 and 2024. Studies were selected based on relevance to the role of inflammation in CA-CRC, specifically targeting molecular pathways and clinical implications. Both clinical and mechanistic studies were reviewed.ConclusionSustained inflammation in the colon fosters a pro-tumorigenic environment, leading to the initiation and progression of CA-CRC. Prevention strategies must focus on controlling chronic inflammation, optimizing IBD management, and implementing regular screenings. Emerging therapies targeting key inflammatory pathways and immune responses, along with microbiome modulation, hold promise for reducing CA-CRC risk. Understanding these molecular mechanisms provides a path toward personalized treatment and better outcomes for patients with IBD at risk of colorectal cancer.
引用
收藏
页数:15
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