Protein Kinase C in Cancer Signaling and Therapy [electronic resource] /
Kazanietz, Marcelo G.editor.
Protein kinase C (PKC), a family of serine-threonine kinases, rocketed to the forefront of the cancer research field in the early 1980’s with its identification as an effector of phorbol esters, natural products with tumor-promoting activity. Phorbol esters had long been of interest to the cancer research field due to early studies in the mouse skin carcinogenesis model, which showed that prolonged topical application of phorbol esters promoted the formation of skin tumors on mice previously treated with mutagenic agents. Research in the last years has established key roles for PKC isozymes in the control of cell proliferation, migration, adhesion, and malignant transformation. In addition, there is a large body of evidence linking PKC to invasion and cancer cell metastasis. It is now well established that the expression of PKC isozymes is altered in various types of cancers. More importantly, small molecule inhibitors have been developed with significant anti-cancer activity. The relevance of PKC isozymes in cancer signaling is therefore remarkable. Protein Kinase C in Cancer Signaling and Therapy is composed of twenty-three chapters written by leading experts in the field. The book is divided into four sections: Regulation of PKC isozyme function: from genes to biochemistry, PKC isozymes in the control of cell function, PKC isozymes in cancer, and PKC isozymes as targets for cancer therapy. Each section of Protein Kinase C in Cancer Signaling and Therapy begins with an introduction by an established professional in the field of Protein kinase C, followed by chapters that elucidate the importance of PKC in current cancer research.
Description based upon print version of record.
Includes bibliographical references and index.
Regulation of PKC Isozyme Function: From Genes to Biochemistry -- Protein Kinase C in Cancer Signaling and Therapy: Introduction and Historical Perspective -- Regulation of Conventional and Novel Protein Kinase C Isozymes by Phosphorylation and Lipids -- Phorbol Esters and Diacylglycerol: The PKC Activators -- Diacylglycerol Signaling: The C1 Domain, Generation of DAG, and Termination of Signals -- Regulation of PKC by Protein–Protein Interactions in Cancer -- PKC Isozymes in the Control of Cell Function -- Introduction: PKC Isozymes in the Control of Cell Function -- Regulation and Function of Protein Kinase D Signaling -- PKC and Control of the Cell Cycle -- PKC and the Control of Apoptosis -- Atypical PKCs, NF-?B, and Inflammation -- PKC Isozymes in Cancer -- Introduction: PKC and Cancer -- Protein Kinase C, p53, and DNA Damage -- PKCs as Mediators of the Hedgehog and Wnt Signaling Pathways -- PKC–PKD Interplay in Cancer -- Transgenic Mouse Models to Investigate Functional Specificity of Protein Kinase C Isoforms in the Development of Squamous Cell Carcinoma, a Nonmelanoma Human Skin Cancer -- PKC Isozymes and Skin Cancer -- PKC and Breast Cancer -- PKC and Prostate Cancer -- Protein Kinase C and Lung Cancer -- PKC Isozymes as Targets for Cancer Therapy -- PKC and Resistance to Chemotherapeutic Agents -- PKC? as a Target for Chemotherapeutic Drugs -- Atypical PKCs as Targets for Cancer Therapy.
Protein kinase C (PKC), a family of serine-threonine kinases, rocketed to the forefront of the cancer research field in the early 1980’s with its identification as an effector of phorbol esters, natural products with tumor-promoting activity. Phorbol esters had long been of interest to the cancer research field due to early studies in the mouse skin carcinogenesis model, which showed that prolonged topical application of phorbol esters promoted the formation of skin tumors on mice previously treated with mutagenic agents. Research in the last years has established key roles for PKC isozymes in the control of cell proliferation, migration, adhesion, and malignant transformation. In addition, there is a large body of evidence linking PKC to invasion and cancer cell metastasis. It is now well established that the expression of PKC isozymes is altered in various types of cancers. More importantly, small molecule inhibitors have been developed with significant anti-cancer activity. The relevance of PKC isozymes in cancer signaling is therefore remarkable. Protein Kinase C in Cancer Signaling and Therapy is composed of twenty-three chapters written by leading experts in the field. The book is divided into four sections: Regulation of PKC isozyme function: from genes to biochemistry, PKC isozymes in the control of cell function, PKC isozymes in cancer, and PKC isozymes as targets for cancer therapy. Each section of Protein Kinase C in Cancer Signaling and Therapy begins with an introduction by an established professional in the field of Protein kinase C, followed by chapters that elucidate the importance of PKC in current cancer research.
Cancer research.
Pharmacology.
Cancer Research.
Pharmacology/Toxicology.