IngentaConnect Protein Kinase C-theta (PKCtheta), a Potential Drug Target for Th...

Abstract:

The link between apoptosis and malignant cell growth is firmly established, and various forms of therapy in cancer, e.g., the use of DNA-damaging chemotherapeutic drugs, are based on the principle of inducing apoptosis in malignant cells. However, in many known instances, tumor cells develop resistance to apoptosis through various mechanisms. Thus, interventions designed to facilitate tumor cells apoptosis are likely to have a therapeutic benefit. PKC thgr , which is expressed relatively selectively in T cells, plays an important role in mature T cell activation and proliferation upon its translocation to the plasma membrane. PKC thgr is necessary for induction of the interleukin-2 (IL-2) gene because the transcription factors AP-1 and NF-kB, which are essential for IL-2 gene promoter activation, are main targets of PKC thgr . Recent studies revealed that PKC thgr provides an important survival signal that protects leukemic T cells from Fas- or UV-induced apoptosis. These findings and the constitutive localization of PKC thgr in the membrane of some leukemic T cells suggests that it plays a role in leukemic T cell survival and / or proliferation, and that selective PKC thgr -inhibitory strategies may facilitate elimination of malignant T cells. The high-affinity IL-2 receptor (IL-2R agr ) is a major target of receptor-directed therapy in several human diseases, and it is constitutively expressed by the malignant cells in some T cell leukemias, suggesting an autocrine IL-2 / IL-2R loop that participates in the expansion of leukemic IL-2R+ cells. Therefore, given the essential role of PKC thgr in IL-2 production, IL-2 gene regulation by PKC thgr could also be of therapeutic interest.

Keywords: pkco; t cell leukemia; ap-I; nf-kb; Il-2r; Il-2r cells

Language: English

Document Type: Review article

DOI: 10.2174/1568009023333908

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Protein Kinase C- (PKC), a Potential Drug Target for Therapeutic Intervention with Human T Cell Leukemias