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Activation of Protein Kinase G Increases the Expression of p21^CIP1, p27^KIP1, and Histidine Triad Protein 1 through Sp1

¹ Herbert Irving Comprehensive Cancer Center, and ² Department of Medicine, College of Physicians and Surgeons, Columbia University, New York, New York

Requests for reprints: I. Bernard Weinstein, Herbert Comprehensive Cancer Center, College of Physicians and Surgeons, Columbia University, 701 West 168th Street, HHSC1509, New York, NY 10032. Phone: 212-305-6921; Fax: 212-305-6889; E-mail: ibw1{at}columbia.edu.

Key Words: PKG • p21 • p27 • HINT1 • Sp1

The anticancer role of cyclic guanosine 3',5'-monophosphate (cGMP)–dependent protein kinase G (PKG) has become of considerable interest, but the underlying mechanisms are not fully established. In this study, we examined the effects of activation of PKG on the expression of three tumor suppressor proteins in human SW480 colon cancer cells. Our results revealed that treatment with cell permeable cGMP derivatives, or the cGMP phosphodiesterase inhibitor sulindac sulfone (exisulind, aptosyn, hereafter called exisulind) led to increased expression of the tumor suppressor proteins p21^CIP1, p27^KIP1, and Histidine triad protein 1 (HINT1), and their corresponding mRNAs. Overexpression of PKG Iβ also caused increased expression of the p21^CIP1, p27^KIP1, and HINT1 proteins. Both the p21^CIP1 and p27^KIP1 promoters contain Sp1 binding sites and they were activated by PKG in luciferase reporter assays. Specific Sp1 sites in the p21 and p27 promoters were sufficient to mediate PKG-induced luciferase reporter activity, suggesting an interaction between Sp1 and PKG. Indeed, we found that PKG can phosphorylate Sp1 on serine residue(s) and this resulted in transcriptional activation of Sp1. Knockdown of Sp1 expression with siRNA inhibited the increased expression of p21^CIP1, p27^KIP1, and HINT1 induced by the cGMP derivative 8-pCPT-cGMP in SW480 cells. These novel effects of PKG activation on the expression of three tumor suppressor genes may explain, at least in part, the anticancer effects of activation of PKG. They also provide a rationale for further developing activators of PKG for the prevention and treatment of cancer. [Cancer Res 2008;68(13):5355–62]