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[Cancer Research 59, 2829-2833, June 1, 1999]
© 1999 American Association for Cancer Research

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[Cancer Research 59, 2829-2833, June 15, 1999]
© 1999 American Association for Cancer Research


Advances in Brief

Implication of p53 in Growth Arrest and Apoptosis Induced by the Synthetic Retinoid CD437 in Human Lung Cancer Cells1

Shi-Yong Sun2, Ping Yue, Gen Sheng Wu, Wafik S. El-Deiry, Braham Shroot, Waun K. Hong and Reuben Lotan

Department of Thoracic/Head and Neck Medical Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030 [S-Y. S., P. Y., W. K. H., R. L.]; Laboratory of Molecular Oncology and Cell Cycle Regulation, Howard Hughes Medical Institute, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104 [G. S. W., W. S. E.]; and Galderma Research and Development, 06905 Sophia Antipolis, France [B. S.]

CD437 is a novel retinoid that can induce apoptosis in a variety of tumor cell types by an unknown mechanism. We found that CD437 up-regulated the expression of p21WAF1/CIP1, Bax, and Killer/DR5 and induced G1 arrest and rapid apoptosis in three human non-small cell lung carcinoma cell lines with wild-type p53 but not in five cell lines with mutant p53, suggesting a role for p53 in the effects of CD437. Using H460 cells in which wild-type p53 protein was degraded by transfection of the human papillomavirus 16 E6 (HPV-16 E6) gene and H460 cells transfected with a control plasmid only, we found that CD437 increased p53, p21WAF1/CIP1, Bax, and Killer/DR5 in the control transfectants. In contrast, the constitutive p53 protein level was suppressed, and the ability of CD437 to increase p53 and its downstream genes was compromised in E6 transfectants. In addition, CD437 induced G1 arrest and apoptosis in the control transfectants but not in the E6-transfected cells. These results indicate that p53 plays a role in CD437-induced growth inhibition and apoptosis in human non-small cell lung carcinoma cells.




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Copyright © 1999 by the American Association for Cancer Research.