Study of the human HABP4 protein and its ortholog VIG-1 in Caenorhabditis elegans
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Author(s): |
Glauber da Costa de Brito
Total Authors: 1
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Document type: | Doctoral Thesis |
Press: | São Paulo. |
Institution: | Universidade de São Paulo (USP). Conjunto das Químicas (IQ e FCF) (CQ/DBDCQ) |
Defense date: | 2007-11-26 |
Examining board members: |
Eduardo Moraes Rego Reis;
Alan Mitchell Durham;
Aline Maria da Silva;
Ismael Dale Cotrim Guerreiro da Silva;
Mari Cleide Sogayar
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Advisor: | Eduardo Moraes Rego Reis |
Abstract | |
The clear cell subtype of renal cell carcinoma (RCC) is the most lethal and prevalent cancer of the urinary system. The carcinogenesis in RCC is thought to be associated with changes in the expression of several genes, and this alteration in gene expression is believed to be critical to the development of the malignant phenotype. To investigate new genes and molecular pathways associated with malignant transformation in clear cell RCC, gene expression profiles of matched samples of tumor and adjacent non-neoplastic tissue obtained from 6 patients were analysed. A custom-built cDNA microarray platform was used, comprising 2,292 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 64 transcripts with levels significantly deregulated in clear cell RCC relative to the matched non-tumor tissue, mostly (86%) downregulated in CCR, was (AU) |