Molecular Mechanisms of SKP2 Targeting on Prostate Cancer Progression
Molecular Mechanisms of SKP2 Targeting on Prostate Cancer Progression
批准号:
8340131
负责人:
LYNN M MATRISIAN
金额:
$7.39万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-09-23 至 2016-08-31
关键词:
African AmericanAmericanAndrogensCancer ControlCancer PatientCastrationCaucasiansCaucasoid RaceDeath RateDiseaseEthnic groupGrowthIncidenceInvestigationMalignant NeoplasmsMalignant neoplasm of prostateMolecularOperative Surgical ProceduresPathway interactionsRaceRadiation therapyRegulationResistanceRoleSKP2 geneSignal PathwayThe Vanderbilt-Ingram Cancer Center at the Vanderbilt Universitycancer diagnosiscancer health disparitycancer statisticsdeprivationmalemenmortalitytumor progression
中文摘要
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英文摘要
Prostate cancer (PCa) is a prevailing disease found in African American men, and is the most
frequently diagnosed cancer in American men. African American males died of PCa in a 2.39-folder higher rate
as compared with Caucasian males, while the average death rate due to all cancers was only 1.34-fold higher
between these two races (Cancer Statistics 2010)^¿. Surgery, radiation therapy and androgen-deprivation
therapy have been developed and applied widely to control PCa; however, prostate cancer patients still died of
Castration Resistant Prostate Cancer (CRPC). Molecular signaling pathways contributing to the initiation and
progression of PCa; particularly, the mechanism of CRPC growth remain to be elucidated in order to develop
efficient strategies for cancer control. Aberrant regulation of Pten-PI3K-Akt pathway, p53 loss and Skp2
activation are commonly found in CRPC. Further investigation on their roles in PCa progression will help us to
understand the incidence and mortality rate of PCa, and the disparities among ethnic and racial groups.
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