Pharmacological modulation of mitochondrial function as novel strategies for treating intestinal inflammatory diseases and colorectal cancer.
10.1016/j.jpha.2024.101074
- Author:
Boya WANG
1
;
Xinrui GUO
1
;
Lanhui QIN
2
;
Liheng HE
1
;
Jingnan LI
1
;
Xudong JIN
3
;
Dapeng CHEN
1
;
Guangbo GE
2
Author Information
1. Department of Comparative Medicine, Dalian Medical University, Dalian, Liaoning, 116044, China.
2. Department of Interdisciplinary Integrative Medicine Research, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.
3. St. Hilda's College, Oxford University, Oxford, OX4 1DY, UK.
- Publication Type:Review
- Keywords:
Colorectal cancer;
Inflammatory bowel disease;
Mitochondria;
Mitochondrial DNA;
Pharmacology
- From:
Journal of Pharmaceutical Analysis
2025;15(4):101074-101074
- CountryChina
- Language:English
-
Abstract:
Inflammatory bowel disease (IBD) is a chronic and recurrent intestinal disease, and has become a major global health issue. Individuals with IBD face an elevated risk of developing colorectal cancer (CRC), and recent studies have indicated that mitochondrial dysfunction plays a pivotal role in the pathogenesis of both IBD and CRC. This review covers the pathogenesis of IBD and CRC, focusing on mitochondrial dysfunction, and explores pharmacological targets and strategies for addressing both conditions by modulating mitochondrial function. Additionally, recent advancements in the pharmacological modulation of mitochondrial dysfunction for treating IBD and CRC, encompassing mitochondrial damage, release of mitochondrial DNA (mtDNA), and impairment of mitophagy, are thoroughly summarized. The review also provides a systematic overview of natural compounds (such as flavonoids, alkaloids, and diterpenoids), Chinese medicines, and intestinal microbiota, which can alleviate IBD and attenuate the progression of CRC by modulating mitochondrial function. In the future, it will be imperative to develop more practical methodologies for real-time monitoring and accurate detection of mitochondrial function, which will greatly aid scientists in identifying more effective agents for treating IBD and CRC through modulation of mitochondrial function.
