Revisiting Telomere Shortening in Cancer Biology Diagrams Aging is a biological process characterized by a progressive functional decline in tissues and organs, which eventually leads to mortality. Telomeres, the repetitive DNA repeat sequences at the end of linear eukaryotic chromosomes protecting chromosome ends from degradation and illegitimate recombination, play a crucial role in cell fate and aging. Telomerase, the enzyme that reduces telomere shortening in certain cells, is reactivated or increased in more than 90 percent of cancers, found a 2016 study. Remember, this enzyme isn't found in Each time a cell divides, 25-200 base pairs are lost from the terminal sequence of chromosomes. By becoming truncated during cell division, telomeres protect essential genes from being shortened and thus inactivated. In addition, telomeres are sensitive to inflammation and oxidative stress, which can further promote telomere shortening.
Persistent low-grade inflammation, common in aging and autoimmune conditions, accelerates telomere shortening by increasing cell turnover and exposure to damaging byproducts. The concept of "inflammaging," describing the chronic pro-inflammatory state associated with aging, explains how sustained immune activation depletes telomeres. Telomere shortening leads to senescence, fibrosis, inflammation and stem cell depletion in the presence of a functional p53 checkpoint. These processes lead to aging and other degenerative and inflammatory diseases. Telomerase activators and senolytics can inhibit these processes and inhibit aging and age related diseases.
Telomere dysfunction in ageing and age Biology Diagrams
Telomere shortening is most pronounced during bone marrow resection, as it has been observed that there is an inverse correlation between the number of transplanted mononuclear cells and the degree of telomere shortening. A bone marrow transplant results in a telomere shortening equivalent to a period of 15 years of life .
Telomere shortening can act as a tumor suppressor. However, as a downside, there is growing evidence indicating that telomere shortening also limits stem cell function, regeneration, and organ maintenance during ageing. Moreover, telomere shortening during ageing and disease is associated with increasing cancer risk.
Hibernating Lemurs Can Turn Back the Clock on Cellular Aging Biology Diagrams
Telomere dysfunction during ageing. As replicative cellular senescence is caused by telomere shortening below a critical length 1, the effect of telomere shortening on organismal ageing in animal
