RESUMO
Mouse double minute 2 (Mdm2) gene was isolated from a cDNA library derived from transformed mouse 3T3 cells, and was classified as an oncogene as it confers 3T3 and Rat2 cells tumorigenicity when overexpressed. It encodes a nucleocytoplasmic shuttling ubiquitin E3 ligase, with its main target being tumor suppressor p53, which is mutated in more than 50% of human primary tumors. Mdm2's oncogenic activity is mainly mediated by p53, which is activated by various stresses, especially genotoxic stress, via Atm (ataxia telangiectasia mutated) and Atr (Atm and Rad3-related). Activated p53 inhibits cell proliferation, induces apoptosis or senescence, and maintains genome integrity. Mdm2 is also a target gene of p53 transcription factor. Thus, Mdm2 and p53 form a feedback regulatory loop. External and internal cues, through multiple signaling pathways, can act on Mdm2 to regulate p53 levels and cell proliferation, death, and senescence. This review will focus on how Mdm2 is regulated under genotoxic stress, and by the Akt1-mTOR-S6K1 pathway that is activated by insulin, growth factors, amino acids, or energy status.
Assuntos
Animais , Humanos , Camundongos , Células 3T3 , Apoptose , Proliferação de Células , Senescência Celular , Dano ao DNA , Metabolismo Energético , Retroalimentação Fisiológica , Biblioteca Gênica , Peptídeos e Proteínas de Sinalização Intercelular , Metabolismo , Terapia de Alvo Molecular , Mutação , Neoplasias , Genética , Metabolismo , Proteínas Proto-Oncogênicas c-mdm2 , Genética , Metabolismo , Proteínas Quinases S6 Ribossômicas 90-kDa , Genética , Metabolismo , Transdução de Sinais , Genética , Serina-Treonina Quinases TOR , Genética , Metabolismo , Proteína Supressora de Tumor p53 , Genética , Metabolismo , Ubiquitina-Proteína Ligases , Genética , MetabolismoRESUMO
0.05).Conclusion There is susceptibility correlation between the UC patients of north Chinese and the rising of C/T gene polymorphisms and T allele gene frequency in IL-1B +3962 site,but there isn't correlation between the gene polymorphisms in IL-1B +3962 site and different invasion location of UC of north Chinese.IFN-?+874 hasn't correlation with UC of north Chinese.