Age-related dysregulation of intestinal epithelium fucosylation is linked to an increased risk of colon cancer

  • JCI Insight. 2024 Mar 8;9(5):e167676. doi: 10.1172/jci.insight.167676.
Zhihan Wang  1  2 Pan Gao  3  4 Kai Guo  4  5 Grace Schirrick  1 Jappreet Singh Gill  1 Jett Weis  1 Abby Lund Da Costa  1 Mansib Rahman  1 Het Mehta  1 Julia Fleecs  1 Shilpi Jain  1 Trishna Debnath  1 Junguk Hur  4 Nadeem Khan  6 Robert Sticca  7 Holly M Brown-Borg  4 Donald A Jurivich  1 Ramkumar Mathur  1
Affiliations
  • 1. Department of Geriatrics, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, North Dakota, USA.
  • 2. State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, West China School of Basic Medical Sciences & Forensic Medicine, and Collaborative Innovation Center for Biotherapy, Sichuan University, Chengdu, China.
  • 3. Department of Urology, Frontier Science Center for Immunology and Metabolism, and Medical Research Institute, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, China.
  • 4. Department of Biomedical Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, North Dakota, USA.
  • 5. Department of Neurology, University of Michigan School of Medicine, Ann Arbor, Michigan, USA.
  • 6. Department of Oral Biology, College of Dentistry, University of Florida, Gainesville, Florida, USA.
  • 7. Department of Surgery, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, North Dakota, USA.
Abstract

Colon Cancer affects people of all ages. However, its frequency, as well as the related morbidity and mortality, are high among older adults. The complex physiological changes in the aging gut substantially limit the development of Cancer therapies. Here, we identify a potentially unique intestinal microenvironment that is linked with an increased risk of colon Cancer in older adults. Our findings show that aging markedly influenced persistent fucosylation of the apical surfaces of intestinal epithelial cells, which resulted in a favorable environment for tumor growth. Furthermore, our findings shed light on the importance of the host-commensal interaction, which facilitates the dysregulation of fucosylation and promotes tumor growth as people get older. We analyzed colonic microbial populations at the species level to find changes associated with aging that could contribute to the development of colon Cancer. Analysis of single-cell RNA-sequencing data from previous publications identified distinct epithelial cell subtypes involved in dysregulated fucosylation in older adults. Overall, our study provides compelling evidence that excessive fucosylation is associated with the development of colon Cancer, that age-related changes increase vulnerability to colon Cancer, and that a dysbiosis in microbial diversity and metabolic changes in the homeostasis of older mice dysregulate fucosylation levels with age.

Keywords
Aging; Cellular senescence; Colorectal cancer; Drug therapy; Microbiology.
Products