P53-INDEPENDENT INDUCTION OF P21(WAF1) PATHWAY IS PRESERVED DURING TUMOR PROGRESSION

  • Authors:
    • YQ CHEN
    • SC CIPRIANO
    • FH SARKAR
    • JL WARE
    • JM ARENKIEL
  • View Affiliations

  • Published online on: October 1, 1995     https://doi.org/10.3892/ijo.7.4.889
  • Pages: 889-893
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Abstract

The p21(WAF1) gene encodes a cyclin-dependent kinase inhibitor and plays an important role in controlling the cell cycle. Its expression can be induced through wild-type p53-dependent or -independent pathways. Since the p53-dependent pathway is disrupted in more than 50% of human tumors, we wondered whether the p53-independent pathway is also altered during tumor progression. In the present study, we have determined p21(WAF1) induction by mitogenic stimuli, which is known to be a p53-independent process. p21(WAF1) is induced by mitogenic stimuli in all cell lines tested regardless of the status of p53, i.e. wild-type, wild-type inactivated by SV40T or mutant, and the transformation of cells from immortal to tumorigenic and to metastatic. These results indicate that the p53-independent induction of p21(WAF1) pathway is preserved during tumor progression.

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October 1995
Volume 7 Issue 4

Print ISSN: 1019-6439
Online ISSN:1791-2423

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Spandidos Publications style
CHEN Y, CIPRIANO S, SARKAR F, WARE J and ARENKIEL J: P53-INDEPENDENT INDUCTION OF P21(WAF1) PATHWAY IS PRESERVED DURING TUMOR PROGRESSION. Int J Oncol 7: 889-893, 1995
APA
CHEN, Y., CIPRIANO, S., SARKAR, F., WARE, J., & ARENKIEL, J. (1995). P53-INDEPENDENT INDUCTION OF P21(WAF1) PATHWAY IS PRESERVED DURING TUMOR PROGRESSION. International Journal of Oncology, 7, 889-893. https://doi.org/10.3892/ijo.7.4.889
MLA
CHEN, Y., CIPRIANO, S., SARKAR, F., WARE, J., ARENKIEL, J."P53-INDEPENDENT INDUCTION OF P21(WAF1) PATHWAY IS PRESERVED DURING TUMOR PROGRESSION". International Journal of Oncology 7.4 (1995): 889-893.
Chicago
CHEN, Y., CIPRIANO, S., SARKAR, F., WARE, J., ARENKIEL, J."P53-INDEPENDENT INDUCTION OF P21(WAF1) PATHWAY IS PRESERVED DURING TUMOR PROGRESSION". International Journal of Oncology 7, no. 4 (1995): 889-893. https://doi.org/10.3892/ijo.7.4.889