Identification of protein-coding and intronic noncoding RNAs down-regulated in clear cell renal carcinoma

Identification of protein-coding and intronic noncoding RNAs down-regulated in clear cell renal carcinoma

Author Brito, Glauber Costa Google Scholar
Fachel, Angela A. Google Scholar
Vettore, Andre Luiz Autor UNIFESP Google Scholar
Vignal, Giselle M. Google Scholar
Gimba, Etel R. P. Google Scholar
Campos, Franz S. Google Scholar
Barcinski, Marcello A. Google Scholar
Verjovski-Almeida, Sergio Google Scholar
Reis, Eduardo M. Google Scholar
Institution Universidade de São Paulo (USP)
Universidade Federal de São Paulo (UNIFESP)
Hosp Canc
Abstract The clear cell subtype of renal cell carcinoma (RCC) is the most lethal and prevalent cancer of the urinary system. To investigate the molecular changes associated with malignant transformation in clear cell RCC, the gene expression profiles of matched samples of tumor and adjacent non-neoplastic tissue were obtained from six patients. A custom-built cDNA microarray platform was used, comprising 2292 probes that map to exons of genes and 822 probes for noncoding RNAs mapping to intronic regions. Intronic transcription was detected in all normal and neoplastic renal tissues. A subset of 55 transcripts was significantly down-regulated in clear cell RCC relative to the matched nontumor tissue as determined by a combination of two statistical tests and leave-one-out patient cross-validation. Among the down-regulated transcripts, 49 mapped to untranslated or coding exons and 6 were intronic relative to known exons of protein-coding genes. Lower levels of expression of SIN3B, TRIP3, SYNJ2BP and NDE1 (P<0.02), and of intronic transcripts derived from SND1 and ACTN4 loci (P<0.05), were confirmed in clear cell RCC by Real-time RT-PCR. A subset of 25 transcripts was deregulated in additional six nonclear cell RCC samples, pointing to common transcriptional alterations in RCC irrespective of the histological subtype or differentiation state of the tumor. Our results indicate a novel set of tumor suppressor gene candidates, including noncoding intronic RNAs, which may play a significant role in malignant transformations of normal renal cells. (C) 2008 Wiley-Liss, Inc.
Keywords clear cell renal cell carcinoma
noncoding RNA
intronic transcription
cDNA microarray
tumor suppressor
Language English
Sponsor Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
EMR
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
Date 2008-10-01
Published in Molecular Carcinogenesis. Hoboken: Wiley-liss, v. 47, n. 10, p. 757-767, 2008.
ISSN 0899-1987 (Sherpa/Romeo, impact factor)
Publisher Wiley-Blackwell
Extent 757-767
Origin http://dx.doi.org/10.1002/mc.20433
Access rights Closed access
Type Article
Web of Science ID WOS:000259764100004
URI http://repositorio.unifesp.br/handle/11600/30931

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