The roles of p27(Kip1) and DNA damage signalling in the chemotherapy-induced delayed cell cycle checkpoint
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
20716117
PubMed Central
PMC3822566
DOI
10.1111/j.1582-4934.2010.01145.x
PII: JCMM1145
Knihovny.cz E-zdroje
- Klíčová slova
- ATM, ATR, DNA damage response, DNA-PKcs, SKP2, cell cycle arrest, chemotherapy, p27Kip1, p38-MAPK,
- MeSH
- ATM protein antagonisté a inhibitory MeSH
- buňky A549 MeSH
- chromony farmakologie MeSH
- doxorubicin farmakologie MeSH
- inhibitor p27 cyklin-dependentní kinasy fyziologie MeSH
- kofein farmakologie MeSH
- kontrolní body fáze G2 buněčného cyklu účinky léků MeSH
- lidé MeSH
- mitogenem aktivované proteinkinasy p38 metabolismus MeSH
- morfoliny farmakologie MeSH
- poškození DNA MeSH
- proteinkinasa aktivovaná DNA antagonisté a inhibitory MeSH
- proteiny asociované s kinázou S-fáze metabolismus MeSH
- protinádorové látky farmakologie MeSH
- pyrony farmakologie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 2-morpholin-4-yl-6-thianthren-1-yl-pyran-4-one MeSH Prohlížeč
- 8-dibenzothiophen-4-yl-2-morpholin-4-yl-chromen-4-one MeSH Prohlížeč
- ATM protein, human MeSH Prohlížeč
- ATM protein MeSH
- CDKN1B protein, human MeSH Prohlížeč
- chromony MeSH
- doxorubicin MeSH
- inhibitor p27 cyklin-dependentní kinasy MeSH
- kofein MeSH
- mitogenem aktivované proteinkinasy p38 MeSH
- morfoliny MeSH
- proteinkinasa aktivovaná DNA MeSH
- proteiny asociované s kinázou S-fáze MeSH
- protinádorové látky MeSH
- pyrony MeSH
DNA lesions trigger the DNA damage response (DDR) machinery, which protects genomic integrity and sustains cellular survival. Increasing data underline the significance of the integrity of the DDR pathway in chemotherapy response. According to a recent work, persistent exposure of A549 lung carcinoma cells to doxorubicin induces an initial DDR-dependent checkpoint response, followed by a later DDR-independent, but p27(Kip1)-dependent one. Prompted by the above report and to better understand the involvement of the DDR signaling after chemotherapeutic stress, we examined the potential role of the canonical DDR pathway in A549 cells treated with doxorubicin. Exposure of A549 cells, prior to doxorubicin treatment, to ATM, ATR and DNA-PKcs inhibitors either alone or in various combinations, revealed that the earlier documented two-step response was DDR-dependent in both steps. Notably, inhibition of both ATM and ATR or selective inhibition of ATM or DNA-PKcs resulted in cell-cycle re-entry despite the increased levels of p27(Kip1) at all time points analyzed. We further investigated the regulation of p27(Kip1) protein levels in the particular setting. Our results showed that the protein status of p27(Kip1) is mainly determined by p38-MAPK, whereas the role of SKP2 is less significant in the doxoroubicin-treated A549 cells. Cumulatively, we provide evidence that the DNA damage signaling is responsible for the prolonged cell cycle arrest observed after persistent chemotherapy-induced genotoxic stress. In conclusion, precise identification of the molecular mechanisms that are activated during the chemotherapeutic cycles could potentially increase the sensitization to the therapy applied.
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