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DNA repair and aging: the impact of the p53 family

期刊

AGING-US
卷 7, 期 12, 页码 1050-1065

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/aging.100858

关键词

aging; DNA repair; p53; p63; p73; homologous recombination; Non homologous end joining

资金

  1. AIRC [2014-IG15653, 9979]
  2. Fondazione Roma NCDs grant
  3. Medical Research Council [MC_U132670600] Funding Source: researchfish
  4. MRC [MC_U132670600] Funding Source: UKRI

向作者/读者索取更多资源

Cells are constantly exposed to endogenous and exogenous factors that threaten the integrity of their DNA. The maintenance of genome stability is of paramount importance in the prevention of both cancer and aging processes. To deal with DNA damage, cells put into operation a sophisticated and coordinated mechanism, collectively known as DNA damage response (DDR). The DDR orchestrates different cellular processes, such as DNA repair, senescence and apoptosis. Among the key factors of the DDR, the related proteins p53, p63 and p73, all belonging to the same family of transcription factors, play multiple relevant roles. Indeed, the members of this family are directly involved in the induction of cell cycle arrest that is necessary to allow the cells to repair. Alternatively, they can promote cell death in case of prolonged or irreparable DNA damage. They also take part in a more direct task by modulating the expression of core factors involved in the process of DNA repair or by directly interacting with them. In this review we will analyze the fundamental roles of the p53 family in the aging process through their multifaceted function in DDR.

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