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炎症和免疫系统在结直肠癌发生中的关键作用:全面透视。

The Crucial Role of Inflammation and the Immune System in Colorectal Cancer Carcinogenesis: A Comprehensive Perspective.

机构信息

Surgery, Biochemistry and Immunology Department, School of Medicine, University of Malaga, 29010 Málaga, Spain.

Research Network on Chronic Diseases, Primary Care, and Health Promotion (RICAPPS), Carlos III Health Institute (Instituto de Salud Carlos III), Av. de Monforte de Lemos, 5, 28029 Madrid, Spain.

出版信息

Int J Mol Sci. 2024 Jun 4;25(11):6188. doi: 10.3390/ijms25116188.


DOI:10.3390/ijms25116188
PMID:38892375
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11172443/
Abstract

Chronic inflammation drives the growth of colorectal cancer through the dysregulation of molecular pathways within the immune system. Infiltration of immune cells, such as macrophages, into tumoral regions results in the release of proinflammatory cytokines (IL-6; IL-17; TNF-α), fostering tumor proliferation, survival, and invasion. Tumors employ various mechanisms to evade immune surveillance, effectively 'cloaking' themselves from detection and subsequent attack. A comprehensive understanding of these intricate molecular interactions is paramount for advancing novel strategies aimed at modulating the immune response against cancer.

摘要

慢性炎症通过免疫系统中分子途径的失调驱动结直肠癌的生长。免疫细胞(如巨噬细胞)浸润到肿瘤区域会导致促炎细胞因子(IL-6;IL-17;TNF-α)的释放,促进肿瘤增殖、存活和侵袭。肿瘤采用各种机制逃避免疫监视,有效地“掩盖”自身,使其免受检测和随后的攻击。全面了解这些复杂的分子相互作用对于推进旨在调节针对癌症的免疫反应的新策略至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cb3/11172443/a632b2b17f8f/ijms-25-06188-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cb3/11172443/8a71fe7db905/ijms-25-06188-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cb3/11172443/a632b2b17f8f/ijms-25-06188-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cb3/11172443/8a71fe7db905/ijms-25-06188-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cb3/11172443/a632b2b17f8f/ijms-25-06188-g002.jpg

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[2]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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J Gastrointest Oncol. 2025-4-30

[10]
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Nutrients. 2025-4-15

本文引用的文献

[1]
Genistein-Aspirin Combination Exerts Cytotoxic and Anti-Migratory Effects in Human Colorectal Cancer Cells.

Life (Basel). 2024-5-9

[2]
Aspirin use and changes in circulating tumor DNA levels in patients with metastatic colorectal cancer.

Pak J Pharm Sci. 2024-1

[3]
Which Drugs are More Effective in Preventing Familial Adenomatous Polyposis Progression based on Network Meta-analysis?

Curr Pharm Des. 2024

[4]
Colorectal Cancer: Epidemiology, Risk Factors, and Prevention.

Cancers (Basel). 2024-4-17

[5]
Evaluation of EGFR and COX pathway inhibition in human colon organoids of serrated polyposis and other hereditary cancer syndromes.

Fam Cancer. 2024-11

[6]
Multi-omic profiling reveals associations between the gut microbiome, host genome and transcriptome in patients with colorectal cancer.

J Transl Med. 2024-2-18

[7]
Administration of intestinal mesenchymal stromal cells reduces colitis-associated cancer in C57BL/6J mice modulating the immune response and gut dysbiosis.

Pharmacol Res. 2023-9

[8]
Identification of intestinal microbiome associated with lymph-vascular invasion in colorectal cancer patients and predictive label construction.

Front Cell Infect Microbiol. 2023

[9]
The Notch signaling pathway: a potential target for cancer immunotherapy.

J Hematol Oncol. 2023-5-2

[10]
Global, regional and national burden of inflammatory bowel disease in 204 countries and territories from 1990 to 2019: a systematic analysis based on the Global Burden of Disease Study 2019.

BMJ Open. 2023-3-28

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