Evidence brief · intervention
Telomerase activation
Based on the provided sources, telomerase activation and maintenance are critical mechanisms in oncology and regenerative biology. Malignant cells maintain telomeres through genetic mechanisms that include *TERT* promoter mutations or alterations in telomere(definition)-binding proteins such as ATRX and DAXX, which are frequently observed in gliomas, hepatocellular carcinoma, and aggressive thyroid cancers [1, 3, 6]. Conversely, germline mutations in telomerase components (such as *hTERT* and *hTR*) impair telomerase function, causing premature disease states like idiopathic pulmonary fibrosis and dyskeratosis congenita [5]. In regenerative contexts, transient telomerase induction is being explored as a therapeutic strategy in myogenic progenitor cells to combat stem cell exhaustion and failed tissue regeneration, such as in Duchenne muscular dystrophy [9].
Open
Sources
- [1] Comprehensive and Integrative Genomic Characterization of Hepatocellular Carcinoma
- [2] Arterial Stiffness and Risk of Coronary Heart Disease and Stroke
- [3] TERT promoter mutations occur frequently in gliomas and a subset of tumors derived from cells with low rates of self-renewal
- [4] Macronutrient metabolism by the human gut microbiome: major fermentation by-products and their impact on host health
- [5] Telomerase Mutations in Families with Idiopathic Pulmonary Fibrosis
- [6] Genomic and transcriptomic hallmarks of poorly differentiated and anaplastic thyroid cancers
- [7] Comparison of Allogeneic vs Autologous Bone Marrow–Derived Mesenchymal Stem Cells Delivered by Transendocardial Injection in Patients With Ischemic Cardiomyopathy
- [8] Building roots in a changing environment: implications for root longevity
- [9] TRANSIENT TELOMERASE INDUCTION IN MYOGENIC PROGENITOR CELLS TO OVERCOME STEM CELL EXHAUSTION IN DUCHENNE MUSCULAR DYSTROPHY
- [10] Association Between Circulating PLA2G12B and Diabetic Kidney Disease in Patients with Type 2 Diabetes Mellitus: A Cross-Sectional Study.