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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Main Authors: Diego Marques, Layse Raynara Ferreira-Costa, Lorenna Larissa Ferreira-Costa, Ana Beatriz Bezerra-Oliveira, Romualdo da Silva Correa, Carlos Cesar de Oliveira Ramos, Tatiana Vinasco-Sandoval, Katia de Paiva Lopes, Ricardo Assunção Vialle, Amanda Ferreira Vidal, Vivian Nogueira Silbiger, Ândrea Ribeiro-dos-Santos
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/12/11/3311
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author Diego Marques
Layse Raynara Ferreira-Costa
Lorenna Larissa Ferreira-Costa
Ana Beatriz Bezerra-Oliveira
Romualdo da Silva Correa
Carlos Cesar de Oliveira Ramos
Tatiana Vinasco-Sandoval
Katia de Paiva Lopes
Ricardo Assunção Vialle
Amanda Ferreira Vidal
Vivian Nogueira Silbiger
Ândrea Ribeiro-dos-Santos
author_facet Diego Marques
Layse Raynara Ferreira-Costa
Lorenna Larissa Ferreira-Costa
Ana Beatriz Bezerra-Oliveira
Romualdo da Silva Correa
Carlos Cesar de Oliveira Ramos
Tatiana Vinasco-Sandoval
Katia de Paiva Lopes
Ricardo Assunção Vialle
Amanda Ferreira Vidal
Vivian Nogueira Silbiger
Ândrea Ribeiro-dos-Santos
author_sort Diego Marques
collection DOAJ
description 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 <i>p</i>-values < 0.05 and |Log<sub>2</sub>(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.
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spelling doaj.art-3e7f6639f43448e29d8f0b3d48ebe2002023-11-20T20:21:38ZengMDPI AGCancers2072-66942020-11-011211331110.3390/cancers12113311Role of miRNAs in Sigmoid Colon Cancer: A Search for Potential BiomarkersDiego Marques0Layse Raynara Ferreira-Costa1Lorenna Larissa Ferreira-Costa2Ana Beatriz Bezerra-Oliveira3Romualdo da Silva Correa4Carlos Cesar de Oliveira Ramos5Tatiana Vinasco-Sandoval6Katia de Paiva Lopes7Ricardo Assunção Vialle8Amanda Ferreira Vidal9Vivian Nogueira Silbiger10Ândrea Ribeiro-dos-Santos11Laboratório de Genética Humana e Médica, Universidade Federal do Pará, Av. Augusto Corrêa, 01, Guamá, Belém 66.075-110, BrazilLaboratório de Bioanálise e Biotecnologia Molecular, Universidade Federal do Rio Grande do Norte, Av. Nilo Peçanha, 620, Petrópolis, Natal 59012-300, BrazilLaboratório de Bioanálise e Biotecnologia Molecular, Universidade Federal do Rio Grande do Norte, Av. Nilo Peçanha, 620, Petrópolis, Natal 59012-300, BrazilLaboratório de Bioanálise e Biotecnologia Molecular, Universidade Federal do Rio Grande do Norte, Av. Nilo Peçanha, 620, Petrópolis, Natal 59012-300, BrazilDepartamento de Cirurgia Oncológica, Liga Norte Riograndense Contra o Câncer, R. Mário Negócio, 2267, Quintas, Natal 59040-000, BrazilLaboratório de Patologia e Citopatologia, Liga Norte Riograndense Contra o Câncer, R. Mário Negócio, 2267, Quintas, Natal 59040-000, BrazilLaboratório de Genética Humana e Médica, Universidade Federal do Pará, Av. Augusto Corrêa, 01, Guamá, Belém 66.075-110, BrazilLaboratório de Genética Humana e Médica, Universidade Federal do Pará, Av. Augusto Corrêa, 01, Guamá, Belém 66.075-110, BrazilLaboratório de Genética Humana e Médica, Universidade Federal do Pará, Av. Augusto Corrêa, 01, Guamá, Belém 66.075-110, BrazilLaboratório de Genética Humana e Médica, Universidade Federal do Pará, Av. Augusto Corrêa, 01, Guamá, Belém 66.075-110, BrazilLaboratório de Bioanálise e Biotecnologia Molecular, Universidade Federal do Rio Grande do Norte, Av. Nilo Peçanha, 620, Petrópolis, Natal 59012-300, BrazilLaboratório de Genética Humana e Médica, Universidade Federal do Pará, Av. Augusto Corrêa, 01, Guamá, Belém 66.075-110, BrazilThe 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 <i>p</i>-values < 0.05 and |Log<sub>2</sub>(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.https://www.mdpi.com/2072-6694/12/11/3311biomarkersfield-effectcolorectal cancermiRNome
spellingShingle Diego Marques
Layse Raynara Ferreira-Costa
Lorenna Larissa Ferreira-Costa
Ana Beatriz Bezerra-Oliveira
Romualdo da Silva Correa
Carlos Cesar de Oliveira Ramos
Tatiana Vinasco-Sandoval
Katia de Paiva Lopes
Ricardo Assunção Vialle
Amanda Ferreira Vidal
Vivian Nogueira Silbiger
Ândrea Ribeiro-dos-Santos
Role of miRNAs in Sigmoid Colon Cancer: A Search for Potential Biomarkers
Cancers
biomarkers
field-effect
colorectal cancer
miRNome
title Role of miRNAs in Sigmoid Colon Cancer: A Search for Potential Biomarkers
title_full Role of miRNAs in Sigmoid Colon Cancer: A Search for Potential Biomarkers
title_fullStr Role of miRNAs in Sigmoid Colon Cancer: A Search for Potential Biomarkers
title_full_unstemmed Role of miRNAs in Sigmoid Colon Cancer: A Search for Potential Biomarkers
title_short Role of miRNAs in Sigmoid Colon Cancer: A Search for Potential Biomarkers
title_sort role of mirnas in sigmoid colon cancer a search for potential biomarkers
topic biomarkers
field-effect
colorectal cancer
miRNome
url https://www.mdpi.com/2072-6694/12/11/3311
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