A sensitive array-based assay for identifying multiple TMPRSS2:ERG fusion gene variants

被引:12
作者
Lu, Qing [1 ]
Nunez, Esperanza [2 ]
Lin, Chunrun [2 ]
Christensen, Kimberly [3 ]
Downs, Tracy [1 ,4 ]
Carson, Dennis A. [1 ,5 ]
Wang-Rodriguez, Jessica [1 ,3 ]
Liu, Yu-Tsueng [1 ,5 ]
机构
[1] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Howard Hughes Med Inst, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Pathol, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Dept Surg, La Jolla, CA 92093 USA
[5] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1093/nar/gkn585
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Studies of gene fusions in solid tumors are not as extensive as in hematological malignancies due to several technical and analytical problems associated with tumor heterogeneity. Nevertheless, there is a growing interest in the role of fusion genes in common epithelial tumors after the discovery of recurrent TMPRSS2:ETS fusions in prostate cancer. Among all of the reported fusion partners in the ETS gene family, TMPRSS2:ERG is the most prevalent one. Here, we present a simple and sensitive microarray-based assay that is able to simultaneously determine multiple fusion variants with a single RT-PCR in impure RNA specimens. The assay detected TMPRSS2:ERG fusion transcripts with a detection sensitivity of <10 cells in the presence of more than 3000 times excess normal RNA, and in primary prostate tumors having no >1% of cancer cells. The ability to detect multiple transcript variants in a single assay is critically dependent on both the primer and probe designs. The assay should facilitate clinical and basic studies for fusion gene screening in clinical specimens, as it can be readily adapted to include multiple gene loci.
引用
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页数:8
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