Title of article :
Loss of p53 induces M-phase retardation following G2 DNA damage checkpoint abrogation
Author/Authors :
Minemoto، نويسنده , , Yuzuru and Uchida، نويسنده , , Sanae and Ohtsubo، نويسنده , , Motoaki and Shimura، نويسنده , , Mari and Sasagawa، نويسنده , , Toshiyuki and Hirata، نويسنده , , Masato and Nakagama، نويسنده , , Hitoshi and Ishizaka، نويسنده , , Yukihito and Yamashita، نويسنده , , Katsumi، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2003
Pages :
7
From page :
13
To page :
19
Abstract :
Most cell lines that lack functional p53 protein are arrested in the G2 phase of the cell cycle due to DNA damage. When the G2 checkpoint is abrogated, these cells are forced into mitotic catastrophe. A549 lung adenocarcinoma cells, in which p53 was eliminated with the HPV16 E6 gene, exhibited efficient arrest in the G2 phase when treated with adriamycin. Administration of caffeine to G2-arrested cells induced a drastic change in cell phenotype, the nature of which depended on the status of p53. Flow cytometric and microscopic observations revealed that cells that either contained or lacked p53 resumed their cell cycles and entered mitosis upon caffeine treatment. However, transit to the M phase was slower in p53-negative cells than in p53-positive cells. Consistent with these observations, CDK1 activity was maintained at high levels, along with stable cyclin B1, in p53-negative cells. The addition of butyrolactone I, which is an inhibitor of CDK1 and CDK2, to the p53-negative cells reduced the floating round cell population and induced the disappearance of cyclin B1. These results suggest a relationship between the p53 pathway and the ubiquitin-mediated degradation of mitotic cyclins and possible cross-talk between the G2-DNA damage checkpoint and the mitotic checkpoint.
Keywords :
HPV16E6 gene , G2 checkpoint , p53 , CDK1 , caffeine , cyclin B
Journal title :
Archives of Biochemistry and Biophysics
Serial Year :
2003
Journal title :
Archives of Biochemistry and Biophysics
Record number :
1620275
Link To Document :
بازگشت