Cellular quiescence caused by the Mdm2 inhibitor nutlin-3A
- PMID: 19855165
- DOI: 10.4161/cc.8.22.10121
Cellular quiescence caused by the Mdm2 inhibitor nutlin-3A
Abstract
Cellular senescence is characterized by irreversible loss of proliferative potential and a large, flat cell morphology. Ectopic p21 and doxorubicin induced cellular senescence in HT1080 and WI-38-tert cell lines. In the same cell lines, the Mdm2 inhibitor nutlin-3a induced p53 but, unexpectedly, caused quiescence (reversible arrest) with a small cell morphology. We discuss that Mdm antagonists could be used in combination with chemotherapy to reversibly arrest normal cells, thus protecting them during chemotherapy of cancer (cyclotherapy).
Comment in
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Intriguing novel abilities of Nutlin-3A: induction of cellular quiescence as opposed to cellular senescence--implications for chemotherapy.Cell Cycle. 2009 Nov 15;8(22):3634-5. Cell Cycle. 2009. PMID: 19875921 No abstract available.
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