The roles of p27(Kip1) and DNA damage signalling in the chemotherapy-induced delayed cell cycle checkpoint
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
20716117
PubMed Central
PMC3822566
DOI
10.1111/j.1582-4934.2010.01145.x
PII: JCMM1145
Knihovny.cz E-resources
- Keywords
- ATM, ATR, DNA damage response, DNA-PKcs, SKP2, cell cycle arrest, chemotherapy, p27Kip1, p38-MAPK,
- MeSH
- Ataxia Telangiectasia Mutated Proteins antagonists & inhibitors MeSH
- A549 Cells MeSH
- Chromones pharmacology MeSH
- Doxorubicin pharmacology MeSH
- Cyclin-Dependent Kinase Inhibitor p27 physiology MeSH
- Caffeine pharmacology MeSH
- G2 Phase Cell Cycle Checkpoints drug effects MeSH
- Humans MeSH
- p38 Mitogen-Activated Protein Kinases metabolism MeSH
- Morpholines pharmacology MeSH
- DNA Damage MeSH
- DNA-Activated Protein Kinase antagonists & inhibitors MeSH
- S-Phase Kinase-Associated Proteins metabolism MeSH
- Antineoplastic Agents pharmacology MeSH
- Pyrones pharmacology MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 2-morpholin-4-yl-6-thianthren-1-yl-pyran-4-one MeSH Browser
- 8-dibenzothiophen-4-yl-2-morpholin-4-yl-chromen-4-one MeSH Browser
- ATM protein, human MeSH Browser
- Ataxia Telangiectasia Mutated Proteins MeSH
- CDKN1B protein, human MeSH Browser
- Chromones MeSH
- Doxorubicin MeSH
- Cyclin-Dependent Kinase Inhibitor p27 MeSH
- Caffeine MeSH
- p38 Mitogen-Activated Protein Kinases MeSH
- Morpholines MeSH
- DNA-Activated Protein Kinase MeSH
- S-Phase Kinase-Associated Proteins MeSH
- Antineoplastic Agents MeSH
- Pyrones 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.
See more in PubMed
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