Multiple alternative splicing markers for ovarian cancer

R Klinck, A Bramard, L Inkel, G Dufresne-Martin… - Cancer research, 2008 - AACR
R Klinck, A Bramard, L Inkel, G Dufresne-Martin, J Gervais-Bird, R Madden, ÉR Paquet
Cancer research, 2008AACR
Intense efforts are currently being directed toward profiling gene expression in the hope of
developing better cancer markers and identifying potential drug targets. Here, we present a
sensitive new approach for the identification of cancer signatures based on direct high-
throughput reverse transcription-PCR validation of alternative splicing events. This layered
and integrated system for splicing annotation (LISA) fills a gap between high-throughput
microarray studies and high-sensitivity individual gene investigations, and was created to …
Abstract
Intense efforts are currently being directed toward profiling gene expression in the hope of developing better cancer markers and identifying potential drug targets. Here, we present a sensitive new approach for the identification of cancer signatures based on direct high-throughput reverse transcription-PCR validation of alternative splicing events. This layered and integrated system for splicing annotation (LISA) fills a gap between high-throughput microarray studies and high-sensitivity individual gene investigations, and was created to monitor the splicing of 600 cancer-associated genes in 25 normal and 21 serous ovarian cancer tissues. Out of >4,700 alternative splicing events screened, the LISA identified 48 events that were significantly associated with serous ovarian tumor tissues. In a further screen directed at 39 ovarian tissues containing cancer pathologies of various origins, our ovarian cancer splicing signature successfully distinguished all normal tissues from cancer. High-volume identification of cancer-associated splice forms by the LISA paves the way for the use of alternative splicing profiling to diagnose subtypes of cancer. [Cancer Res 2008;68(3):657–63]
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