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Chinese Journal of Cancer ; (12): 363-364, 2013.
Artigo em Inglês | WPRIM | ID: wpr-320568

RESUMO

Targeted therapies include small-molecule inhibitors and monoclonal antibodies, have made treatment more tumor-specific and less toxic, and have opened new possibilities for tailoring cancer treatment. Nevertheless, there remain several challenges to targeted therapies, including molecular identification, drug resistance, and exploring reliable biomarkers. Here, we present several selected signaling pathways and molecular targets involved in human cancers including Aurora kinases, PI3K/mTOR signaling, FOXO-FOXM1 axis, and MDM2/MDM4-p53 interaction. Understanding the molecular mechanisms for tumorigenesis and development of drug resistance will provide new insights into drug discovery and design of therapeutic strategies for targeted therapies.


Assuntos
Humanos , Aurora Quinases , Metabolismo , Resistencia a Medicamentos Antineoplásicos , Proteína Forkhead Box M1 , Proteína Forkhead Box O3 , Fatores de Transcrição Forkhead , Metabolismo , Terapia de Alvo Molecular , Neoplasias , Metabolismo , Terapêutica , Proteínas Nucleares , Metabolismo , Fosfatidilinositol 3-Quinases , Metabolismo , Proteínas Proto-Oncogênicas , Metabolismo , Proteínas Proto-Oncogênicas c-mdm2 , Metabolismo , Transdução de Sinais , Serina-Treonina Quinases TOR , Metabolismo , Proteína Supressora de Tumor p53 , Metabolismo
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