期刊
ONCOGENE
卷 26, 期 31, 页码 4596-4599出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/sj.onc.1210237
关键词
prostate cancer; cancer-specific death; prognosis; TMPRSS2 : ETS; ERG
资金
- NCI NIH HHS [P50 CA090381, UO1CA113913] Funding Source: Medline
- NIA NIH HHS [R01AG21404] Funding Source: Medline
The identification of the TMPRSS2:ERG fusion in prostate cancer suggests that distinct molecular subtypes may de. ne risk for disease progression. In surgical series, TMPRSS2:ERG fusion was identified in 50% of the tumors. Here, we report on a population-based cohort of men with localized prostate cancers followed by expectant (watchful waiting) therapy with 15% (17/111) TMPRSS2:ERG fusion. We identified a statistically significant association between TMPRSS2:ERG fusion and prostate cancer specific death (cumulative incidence ratio = 2.7, P < 0.01, 95% confidence interval = 1.3-5.8). Quantitative reverse-transcription-polymerase chain reaction demonstrated high estrogen-regulated gene (ERG) expression to be associated with TMPRSS2: ERG fusion (P < 0.005). These data suggest that TMPRSS2:ERG fusion prostate cancers may have a more aggressive phenotype, possibly mediated through increased ERG expression.
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