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Epigenetic modification of the Wnt signaling pathway: a potential target for intestinal aging
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Ji-Da Wang1,#,
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Yue-Xuan Shi1,#,
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Ogbe Susan Enechojo1,2,
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Huan-Tian Cui3,
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Ying Wang1,
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Abankwah Joseph Kofi1,
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Xiang-Ling Wang1,
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Yu-Bong Bian1,* and
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Xiao-Qian Chu1,*
Author information
School of Integrative Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China
Department of Physiology, Federal University, Wukari 670101, Nigeria
First School of Clinical Medicine, Yunnan University of Chinese Medicine, Kunming 650500, China
Correspondence to: Yu-Bong Bian, School of Integrative Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China. E-mail:
bianyuhong_2012@163.com; Xiao-Qian Chu, School of Integrative Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China. E-mail:
chuxiaoqian8@163.com
Abstract
The world has entered an aging society, and it is expected that the global population aged 60 years or older will reach 1.5 billion by 2035. Aging is gradually becoming a major public health issue, posing a significant challenge to healthcare systems. It is a complex natural physiological process involving the irreversible degeneration of body cells, tissues, and organs, and it is a major risk factor for many chronic diseases.
Keywords
Wnt signaling pathway,
intestinal aging,
intestinal stem cells
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Copyright © 2025 Authors.
This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 4.0 License (CC BY-NC 4.0), permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Wang JD, Shi YX, Enechojo OS, Cui HT, Wang Y, Kofi AJ, et al. Epigenetic modification of the Wnt signaling pathway: a potential target for intestinal aging. Gastroenterol & Hepatol Res. 2024;6(2):8. doi: 10.53388/ghr2024008.
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Article History
| Received |
Revised |
Accepted |
Published |
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June 30, 2024
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DOI
http://dx.doi.org/10.53388/ghr2024008
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Gastroenterology & Hepatology Research
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eISSN 2703-173X