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10.3233/ACP-CLO-2010-0533

http://scihub22266oqcxt.onion/10.3233/ACP-CLO-2010-0533
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C4605574!4605574!20966545
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suck abstract from ncbi

pmid20966545      Anal+Cell+Pathol+(Amst) 2010 ; 33 (2): 81-94
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  • Gene Expression in Oligodendroglial Tumors #MMPMID20966545
  • Shaw EJ; Haylock B; Husband D; du Plessis D; Sibson DR; Warnke PC; Walker C
  • Anal Cell Pathol (Amst) 2010[]; 33 (2): 81-94 PMID20966545show ga
  • Background: Oligodendroglial tumors with 1p/19q loss are more likely to be chemosensitive and have longer survival than those with intact 1p/19q, but not all respond to chemotherapy, warranting investigation of the biological basis of chemosensitivity.Methods: Gene expression profiling was performed using amplified antisense RNA from 28 oligodendroglial tumors treated with chemotherapy (26 serial stereotactic biopsy, 2 resection). Expression of differentially expressed genes was validated by real-time PCR.Results: Unsupervised hierarchical clustering showed clustering of multiple samples from the same case in 14/17 cases and identified subgroups associated with tumor grade and 1p/19q status. 176 genes were differentially expressed, 164 being associated with 1p/19q loss (86% not on 1p or 19q). 94 genes differed between responders and non-responders to chemotherapy; 12 were not associated with 1p/19q loss. Significant differential expression was confirmed in 11/13 selected genes. Novel genes associated with response to therapy included SSBP2, GFRA1, FAP and RASD1. IQGAP1, INA, TGIF1, NR2F2 and MYCBP were differentially expressed in oligodendroglial tumors with 1p/19q loss.Conclusion: Gene expression profiling using serial stereotactic biopsies indicated greater homogeneity within tumors than between tumors. Genes associated with 1p/19q status or response were identified warranting further elucidation of their role in oligodendroglial tumors.
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