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


Autoria(s): BRITO, Glauber Costa; FACHEL, Angela A.; VETTORE, Andre Luiz; VIGNAL, Giselle M.; GIMBA, Etel R. P.; CAMPOS, Franz S.; BARCINSKI, Marcello A.; VERJOVSKI-ALMEIDA, Sergio; REIS, Eduardo M.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2008

Resumo

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.

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo

FAPESP

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

EMR

EMR

CNPq Conselho Nacional de Desenvolvimento Cientifico e Tecnologico

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CNPq, Brasil

Identificador

MOLECULAR CARCINOGENESIS, v.47, n.10, p.757-767, 2008

0899-1987

http://producao.usp.br/handle/BDPI/30878

10.1002/mc.20433

http://dx.doi.org/10.1002/mc.20433

Idioma(s)

eng

Publicador

WILEY-LISS

Relação

Molecular Carcinogenesis

Direitos

restrictedAccess

Copyright WILEY-LISS

Palavras-Chave #clear cell renal cell carcinoma #noncoding RNA #intronic transcription #cDNA microarray #tumor suppressor #DIFFERENTIAL GENE-EXPRESSION #ANTISENSE RNA #CANCER #METASTASIS #CLASSIFICATION #TRANSCRIPTOME #TARGETS #DEACETYLASE #SEQUENCES #PATTERNS #Biochemistry & Molecular Biology #Oncology
Tipo

article

original article

publishedVersion