NMD inhibition fails to identify tumour suppressor genes in microsatellite stable gastric cancer cell lines

• Main Authors: Ylstra Bauke (Author), Wiel Mark (Author), Duval Alex (Author), El-Bchiri Jamila (Author), Tijssen Marianne (Author), Buffart Tineke E (Author), Meijer Gerrit A (Author), Carvalho Beatriz (Author)
• Format: Book
• Published: BMC, 2009-06-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Summary

<p>Abstract</p> <p>Background</p> <p>Gastric cancers frequently show chromosomal alterations which can cause activation of oncogenes, and/or inactivation of tumour suppressor genes. In gastric cancer several chromosomal regions are described to be frequently lost, but for most of the regions, no tumour suppressor genes have been identified yet. The present study aimed to identify tumour suppressor genes inactivated by nonsense mutation and deletion in gastric cancer by means of GINI (gene identification by nonsense mediated decay inhibition) and whole genome copy number analysis.</p> <p>Methods</p> <p>Two non-commercial gastric cancer cell lines, GP202 and IPA220, were transfected with siRNA directed against <it>UPF1</it>, to specifically inhibit the nonsense mediated decay (NMD) pathway, and with siRNA directed against non-specific siRNA duplexes (CVII) as a control. Microarray expression experiments were performed in triplicate on 4 × 44 K Agilent arrays by hybridizing RNA from <it>UPF1</it>-transfected cells against non-specific CVII-transfected cells. In addition, array CGH of the two cell lines was performed on 4 × 44K agilent arrays to obtain the DNA copy number profiles. Mutation analysis of GINI candidates was performed by sequencing.</p> <p>Results</p> <p><it>UPF1 </it>expression was reduced for >70% and >80% in the GP202 and IPA220 gastric cancer cell lines, respectively. Integration of array CGH and microarray expression data provided a list of 134 and 50 candidate genes inactivated by nonsense mutation and deletion for GP202 and IPA220, respectively. We selected 12 candidate genes for mutation analysis. Of these, sequence analysis was performed on 11 genes. One gene, <it>PLA2G4A</it>, showed a silent mutation, and in two genes, <it>CTSA </it>and <it>PTPRJ</it>, missense mutations were detected. No nonsense mutations were detected in any of the 11 genes tested.</p> <p>Conclusion</p> <p>Although <it>UPF1 </it>was substantially repressed, thus resulting in the inhibition of the NMD system, we did not find genes inactivated by nonsense mutations. Our results show that the GINI strategy leads to a high number of false positives.</p>

Item Description

10.1186/1755-8794-2-39
1755-8794