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Biol. Res ; 50: 6, 2017. tab, graf
Artigo em Inglês | LILACS | ID: biblio-838962

RESUMO

BACKGROUND: This study aimed to investigate the gene expression changes associated with carcinoma-associated fibroblasts (CAFs) involving in non-small cell lung carcinoma (NSCLC). METHODS: We downloaded the GEO series GSE22862, which contained matched gene expression values for 15 CAF and normal fibroblasts samples, and series GSE27289 containing SNP genotyping for four matched NSCLC samples. The differentially expressed genes in CAF samples were identified using the limma package in R. Then we performed gene ontology (GO) and pathway enrichment analysis and protein-protein interaction (PPI) network construction using the identified DEGs. Moreover, aberrant cell fraction, ploidy, allele-specific copy number, and loss of heterozygosity (LOH) within CAF cells were analyzed using the allele-specific copy number analysis. RESULTS: We obtained 545 differentially expressed genes between CAF and normal fibroblasts samples. The up-regulated genes are mainly involved in GO terms such as positive regulation of cell migration and extracellular region, while the down-regulated genes participate in the lung development and extracellular region. Multiple genes including bone morphogenetic protein 4 (BMP4) and transforming growth factor, beta 3 (TGFB3) are involved in the TGF-ß signaling pathway. Genes including BMP4, TGFBI and matrix Gla protein (MGP) were hub genes. Moreover, no LOH event for BMP4 and MGP was found, that for sphingosine kinase 1 (SPHK1) was 70%, and for TGFBI was 40%. CONCLUSION: Our data suggested that BMP4, MGP, TGFBI, and SPHK1 may be important in CAFs-associated NSCLC, and the abnormal expression and high LOH frequency of them may be used as the diagnosis targets of CAFs in NSCLC.


Assuntos
Humanos , Carcinoma/genética , Regulação Neoplásica da Expressão Gênica , Carcinoma Pulmonar de Células não Pequenas/genética , Fibroblastos Associados a Câncer , Neoplasias Pulmonares/genética , Carcinoma/patologia , Regulação para Baixo , Regulação para Cima , Fator de Crescimento Transformador beta/genética , Carcinoma Pulmonar de Células não Pequenas/patologia , Dosagem de Genes , Perda de Heterozigosidade , Perfilação da Expressão Gênica , Análise Serial de Tecidos , Alelos , Estudos de Associação Genética , Mapas de Interação de Proteínas , Ontologia Genética , Neoplasias Pulmonares/patologia
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