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[Cancer Research 56, 31-35, January 1, 1996]
© 1996 American Association for Cancer Research

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Regulation of p21WAF1/CIP1 Expression through Mitogen-activated Protein Kinase Signaling Pathway

Yusen Liu, Jennifer L. Martindale, Myriam Gorospe and Nikki J. Holbrook1

Gene Expression and Aging Section, Laboratory of Cellular and Molecular Biology, Gerontology Research Center, National Institute on Aging, Baltimore, Maryland 21224

p21WAF1/CIP1 is a cyclin-dependent kinase inhibitor whose expression in mammalian tissues is highly induced in response to stress as well as during normal development and differentiation. Induction of p21WAF1/CIP1 in response to DNA damage occurs through a transcriptional mechanism that is dependent on the activation of the tumor suppressor protein p53. Recent evidence indicates that p21WAF1/CIP1 can also be induced independent of p53, but the signal transduction mechanisms involved in regulating p21WAF1/CIP1 expression in these situations have not been elucidated. In this study, we have addressed the role of the mitogen-activated protein kinase signaling pathway in the induction of p21WAF1/CIP1 in response to growth factor treatment. Using an experimental approach involving cotransfection of a p21WAF1/CIP1 promoter-luciferase construct with a variety of plasmids expressing dominant positive or dominant negative mutant proteins involved in this signaling pathway, we provide evidence to support a role for mitogen-activated protein kinase in the transcriptional activation of p21WAF1/CIP1 by growth factor stimulation.

1 To whom requests for reprints should be addressed, at Gene Expression and Aging Section, Laboratory of Cellular and Molecular Biology, Gerontology Research Center, 4940 Eastern Avenue, Baltimore, MD 21224.

Received 9/19/95. Accepted 11/13/95.




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Copyright © 1996 by the American Association for Cancer Research.