Show simple item record

dc.contributor.author Pădure, Cătălina
dc.contributor.author Capcelea, Svetlana
dc.date.accessioned 2020-11-09T11:58:28Z
dc.date.available 2020-11-09T11:58:28Z
dc.date.issued 2020-10
dc.identifier.uri http://repository.usmf.md/handle/20.500.12710/12720
dc.identifier.uri https://stiinta.usmf.md/ro/manifestari-stiintifice/zilele-universitatii
dc.description Department of Molecular Biology and Human Genetics, State University of Medicine and Pharmacy "Nicolae Testemiteanu" Chișinău, Republic of Moldova, Congresul consacrat aniversării a 75-a de la fondarea Universității de Stat de Medicină și Farmacie „Nicolae Testemițanu” din Republica Moldova, Ziua internațională a științei pentru pace și dezvoltare en_US
dc.description.abstract Introduction: Senescence is the last stage of the physiological development of the human body, in which the cell division stops and the accumulation of damaged cells takes place. Trigger factors are DNA damage, telomere shortening, activation of oncogenic mutations/inactivation of tumor suppressor genes. Purpose: The correlation between the molecular-genetic aspects of senescence and the exponential increase in the risk of developing malignant tumors with age. Material and methods: Analysis of 25 PubMed scientific articles. Results: Senescence has an impact on aging through 2 mechanisms: 1st With age senescent cells accumulate in tissues, maintaining their status like this for years, affecting the normal structure and function. 2nd Senescence can limit the regenerative potential of adult stem cells. One explanation is that aged organisms accumulate more genetic, epigenetic changes than young do. Having shorter telomeres, higher levels of damaged DNA, aged organisms are more resistant to oncogene proliferation than young are. Studies have shown that a higher incidence of malignancies in old age reflects the time required for the accumulation of oncogenic mutations. Besides aging and cancer, the same mechanisms of cellular senescence can contribute to the development of cardiovascular diseases, atherosclerosis, type 2 diabetes, osteoarthritis, sarcopenia, neurodegenerative disorders etc. Conclusions: Despite the fact that the genetic program in Homo sapiens provides a longevity of 140 years, the average age is 72.28 years (according to United Nations, World Population Prospects 2019). Numerous genetic factors both inherited and acquired, internal and external environmental factors can accelerate program depletion, cell senescence, aging of the body and the development of cancer. Considering that senescence can have both bene􀏐icial and detrimental effects, pro-senescence and anti-senescence approaches could improve research into the treatment of the age-related diseases, prevention of many geriatric problems and improving the general health span of aged individuals. en_US
dc.language.iso en en_US
dc.publisher Universitatea de Stat de Medicină şi Farmacie "Nicolae Testemiţanu" en_US
dc.subject senescence en_US
dc.subject oncogenic mutations en_US
dc.subject DNA en_US
dc.subject aging en_US
dc.subject cancer en_US
dc.title Molecular and genetic aspects of senescence en_US
dc.type Other en_US


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search DSpace


Advanced Search

Browse

My Account

Statistics