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Updated: May 20, 2025

Techniques to Induce and Quantify Cellular Senescence
Published on: May 1, 2017
Epigenetic Regulation of Cellular Senescence in Gastrointestinal Cancer
Ting Ye1, Hang Gao1, Zheng-Rong Zhang1
1School of Integrated Chinese and Western Medicine, Anhui University of Chinese Medicine, Hefei, China.
None:
Gastrointestinal (GI) cancers, encompassing malignancies of the digestive tract, are significant contributors to global cancer morbidity and mortality. Despite advancements in molecular insights and therapeutic approaches, the prognosis remains dismal because of persistent treatment resistance and metastasis. Cellular senescence, a permanent halt in the cell cycle due to various stressors, plays dual roles in tumor suppression and promotion. Interestingly, epigenetic modifications, heritable shifts in gene level without altering the DNA sequence, are identified as key regulators of cellular senescence. These modifications, such as DNA methylation, histone alterations, chromatin remodeling, and noncoding RNA interactions, shape the senescence phenotype and influence cancer progression and therapy resistance. Recent research underscores the potential of "pro-senescence" therapies, leveraging epigenetic modulators and senescence-inducing agents to counteract GI cancer progression. This review explores the relationship between cellular senescence and epigenetic regulation in the context of GI cancer by highlighting the characteristics of senescence, the epigenetic mechanisms at play, their impact on GI cancer senescence, and the promising horizon of anti-senescence therapies. Through a detailed examination of current research, we propose that understanding the intricacies of epigenetic regulation in cellular senescence offers a novel vista for therapeutic intervention in GI cancers, potentially paving the way for improved clinical outcomes.
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