DNA is an entity shielded by mechanisms that maintain genomic stability and are essential for living cells; however, DNA is constantly subject to assaults from the environment throughout the cellular life span, making the genome susceptible to mutation and irreparable damage. Cells are prepared to mend such events through cell death as an extrema ratio to solve those threats from a multicellular perspective. However, in cells under various stress conditions, checkpoint mechanisms are activated to allow cells to have enough time to repair the damaged DNA. In yeast, entry into the cell cycle when damage is not completely repaired represents an adaptive mechanism to cope with stressful conditions. In multicellular organisms, entry into cell cycle with damaged DNA is strictly forbidden. However, in cancer development, individual cells undergo checkpoint adaptation, in which most cells die, but some survive acquiring advantageous mutations and selfishly evolve a conflictual behavior. In this review, we focus on how, in cancer development, cells rely on checkpoint adaptation to escape DNA stress and ultimately to cell death.

DNA damage stress: Cui prodest? / Verma, Nagendra; Franchitto, Matteo; Zonfrilli, Azzurra; Cialfi, Samantha; Palermo, Rocco; Talora, Claudio. - In: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. - ISSN 1661-6596. - 20:5(2019). [10.3390/ijms20051073]

DNA damage stress: Cui prodest?

Verma, Nagendra;Franchitto, Matteo;Zonfrilli, Azzurra;Cialfi, Samantha;Palermo, Rocco;Talora, Claudio
2019

Abstract

DNA is an entity shielded by mechanisms that maintain genomic stability and are essential for living cells; however, DNA is constantly subject to assaults from the environment throughout the cellular life span, making the genome susceptible to mutation and irreparable damage. Cells are prepared to mend such events through cell death as an extrema ratio to solve those threats from a multicellular perspective. However, in cells under various stress conditions, checkpoint mechanisms are activated to allow cells to have enough time to repair the damaged DNA. In yeast, entry into the cell cycle when damage is not completely repaired represents an adaptive mechanism to cope with stressful conditions. In multicellular organisms, entry into cell cycle with damaged DNA is strictly forbidden. However, in cancer development, individual cells undergo checkpoint adaptation, in which most cells die, but some survive acquiring advantageous mutations and selfishly evolve a conflictual behavior. In this review, we focus on how, in cancer development, cells rely on checkpoint adaptation to escape DNA stress and ultimately to cell death.
2019
adaptation; cell cycle checkpoints; cell death; G2-arrest; genomic instability; repair of DNA damage; catalysis; molecular biology; spectroscopy; computer science applications1707 computer vision and pattern recognition; physical and theoretical chemistry; organic chemistry; inorganic chemistry
01 Pubblicazione su rivista::01g Articolo di rassegna (Review)
DNA damage stress: Cui prodest? / Verma, Nagendra; Franchitto, Matteo; Zonfrilli, Azzurra; Cialfi, Samantha; Palermo, Rocco; Talora, Claudio. - In: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. - ISSN 1661-6596. - 20:5(2019). [10.3390/ijms20051073]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1258524
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