Role of miRNAs in sigmoid colon cancer: a search for potential biomarkers

The aberrant expression of microRNAs in known to play a crucial role in carcinogenesis. Here, we evaluated the miRNA expression profile of sigmoid colon cancer (SCC) compared to adjacent-to-tumor (ADJ) and sigmoid colon healthy (SCH) tissues obtained from colon biopsy extracted from Brazilian patien...

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Detalles Bibliográficos
Autores: Correa, Romualdo da Silva, Marques, Diego, Costa, Layse Raynara Ferreira, Costa, Lorenna Larissa Ferreira, Oliveira, Ana Beatriz Bezerra, Ramos, Carlos Cesar de Oliveira, Sandoval, Tatiana Vinasco, Lopes, Katia de Paiva, Vialle, Ricardo Assunção, Vidal, Amanda Ferreira, Silbiger, Vivian Nogueira, Santos, Ândrea Ribeiro dos
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2020
País:Brasil
Institución:Universidade Federal do Rio Grande do Norte (UFRN)
Repositorio:Repositório Institucional da UFRN
Idioma:inglés
OAI Identifier:oai:repositorio.ufrn.br:123456789/53101
Acceso en línea:https://repositorio.ufrn.br/handle/123456789/53101
https://doi.org/10.3390/cancers12113311
Access Level:acceso abierto
Palabra clave:biomarkers
field-effect
colorectal cancer
miRNome
Descripción
Sumario:The aberrant expression of microRNAs in known to play a crucial role in carcinogenesis. Here, we evaluated the miRNA expression profile of sigmoid colon cancer (SCC) compared to adjacent-to-tumor (ADJ) and sigmoid colon healthy (SCH) tissues obtained from colon biopsy extracted from Brazilian patients. Comparisons were performed between each group separately, considering as significant p-values < 0.05 and |Log2(Fold-Change)| > 2. We found 20 differentially expressed miRNAs (DEmiRNAs) in all comparisons, two of which were shared between SCC vs. ADJ and SCC vs. SCH. We used miRTarBase, and miRTargetLink to identify target-genes of the differentially expressed miRNAs, and DAVID and REACTOME databases for gene enrichment analysis. We also used TCGA and GTEx databases to build miRNA-gene regulatory networks and check for the reproducibility in our results. As findings, in addition to previously known miRNAs associated with colorectal cancer, we identified three potential novel biomarkers. We showed that the three types of colon tissue could be clearly distinguished using a panel composed by the 20 DEmiRNAs. Additionally, we found enriched pathways related to the carcinogenic process in which miRNA could be involved, indicating that adjacent-to-tumor tissues may be already altered and cannot be considered as healthy tissues. Overall, we expect that these findings may help in the search for biomarkers to prevent cancer progression or, at least, allow its early detection, however, more studies are needed to confirm our results.