| Autor: |
Lichner, Zsuzsanna, Scorilas, Andreas, White, Nicole M.A., Girgis, Andrew H., Rotstein, Lora, Wiegand, Kimberly C., Latif, Ashraf, Chow, Christina, Huntsman, David, Yousef, George M. |
| Zdroj: |
American Journal of Pathology; April 2013, Vol. 182 Issue: 4 p1163-1170, 8p |
| Abstrakt: |
Clear cell renal cell carcinoma (ccRCC) is the most common tumor of the adult kidney, with an increasing rate of incidence. Recently, exome sequencing studies have revealed that the SWI/SNF (switch/sucrose nonfermentable) members PBRM1and ARID1Aare mutated in ccRCC, and it has also been suggested that aberrant chromatin regulation is a key step in kidney cancer pathogenesis. Herein, we show that down-regulation of another SW/SNF component, ARID1A, occurs frequently in ccRCC. We detected copy number loss of ARID1Ain 16% of patients with ccRCC. Immunohistochemistry indicated that 67% of ccRCC (53 of 79) had significantly lower expression of BAF250a, the protein product of ARID1A, than did the matched normal kidney cortex. In parallel, we conducted in silicomRNA expression analysis on 404 ccRCC tumors and 167 normal kidney cortex samples using publicly available databases and confirmed significant down-regulation of ARID1Ain 68.8% of patients. We also show that decreased BAF250a protein and ARID1AmRNA expression correlate with tumor stage and grade. Our results indicate that both the protein and mRNA levels of ARID1Aare statistically significant prognostic markers for ccRCC. Even after controlling for other confounders in the multivariate analysis, BAF250 retained its prognostic significance. BAF250a IHC is easy to perform and represents a potential biomarker that could be incorporated in laboratory practice to enhance the accuracy of the existing prognostic models. |
| Databáze: |
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