
Various kinases phosphorylate their substrates and thereby switch on or off their functions. Dysregulation of kinases that regulate cell growth signals induces carcinogenesis or malignant phenotypes in cancer. Therefore, kinases are considered to be most promising therapeutic targets in cancer treatment, and the development of kinase inhibitors has been the most hot area. In this article, the present status and the perspective of kinase inhibitors were described.
Proto-Oncogene Proteins B-raf, Phosphotransferases, Fusion Proteins, bcr-abl, Antibodies, Monoclonal, Protein-Tyrosine Kinases, Antibodies, Monoclonal, Humanized, Piperazines, Bevacizumab, ErbB Receptors, Antibodies, Monoclonal, Murine-Derived, Genes, ras, Drug Design, Neoplasms, Benzamides, Mutation, Biomarkers, Tumor, Imatinib Mesylate, Humans, Protein Kinase Inhibitors, Phosphoinositide-3 Kinase Inhibitors
Proto-Oncogene Proteins B-raf, Phosphotransferases, Fusion Proteins, bcr-abl, Antibodies, Monoclonal, Protein-Tyrosine Kinases, Antibodies, Monoclonal, Humanized, Piperazines, Bevacizumab, ErbB Receptors, Antibodies, Monoclonal, Murine-Derived, Genes, ras, Drug Design, Neoplasms, Benzamides, Mutation, Biomarkers, Tumor, Imatinib Mesylate, Humans, Protein Kinase Inhibitors, Phosphoinositide-3 Kinase Inhibitors
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