High-Throughput Sequencing of miRNAs Reveals a Tissue Signature in Gastric Cancer and Suggests Novel Potential Biomarkers
Gastric cancer has a high incidence and mortality rate worldwide; however, the use of biomarkers for its clinical diagnosis remains limited. The microRNAs (miRNAs) are biomarkers with the potential to identify the risk and prognosis as well as therapeutic targets. We performed the ultradeep miRnomes...
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doaj-838476e18d3f47dd90744751c5bcb7bf2020-11-25T03:17:11ZengSAGE PublishingBioinformatics and Biology Insights1177-93222015-01-019s110.4137/BBI.S23773High-Throughput Sequencing of miRNAs Reveals a Tissue Signature in Gastric Cancer and Suggests Novel Potential BiomarkersSylvain Darnet0Fabiano C Moreira1Igor G Hamoy2Rommel Burbano3André Khayat4Aline Cruz5Leandro Magalhães6Artur Silva7Sidney Santos8Samia Demachki9Monica Assumpção10Paulo Assumpção11Âuandrea Ribeiro-Dos-Santos12Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, PA, Brazil.Área de Ciências Exatas e Tecnológicas, Centro Universitário do Pará, Belém, PA, Brazil.Universidade Federal Rural da Amazônia, Campus de Capanema, PA, Brazil.Núcleo de Pesquisa em Oncologia, Universidade Federal do Pará, Belém, PA, Brazil.Núcleo de Pesquisa em Oncologia, Universidade Federal do Pará, Belém, PA, Brazil.Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, PA, Brazil.Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, PA, Brazil.Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, PA, Brazil.Núcleo de Pesquisa em Oncologia, Universidade Federal do Pará, Belém, PA, Brazil.Instituto de Ciências da Saúde, Universidade Federal do Pará, Belém, PA, Brazil.Hospital Universitário João de Barros Barreto, Universidade Federal do Pará, Belém, PA, Brazil.Hospital Universitário João de Barros Barreto, Universidade Federal do Pará, Belém, PA, Brazil.Núcleo de Pesquisa em Oncologia, Universidade Federal do Pará, Belém, PA, Brazil.Gastric cancer has a high incidence and mortality rate worldwide; however, the use of biomarkers for its clinical diagnosis remains limited. The microRNAs (miRNAs) are biomarkers with the potential to identify the risk and prognosis as well as therapeutic targets. We performed the ultradeep miRnomes sequencing of gastric adenocarcinoma and gastric antrum without tumor samples. We observed that a small set of those samples were responsible for approximately 80% of the total miRNAs expression, which might represent a miRNA tissue signature. Additionally, we identified seven miRNAs exhibiting significant differences, and, of these, hsa-miR-135b and hsa-miR-29c were able to discriminate antrum without tumor from gastric cancer regardless of the histological type. These findings were validated by quantitative real-time polymerase chain reaction. The results revealed that hsa-miR-135b and hsa-miR-29c are potential gastric adenocarcinoma occurrence biomarkers with the ability to identify individuals at a higher risk of developing this cancer, and could even be used as therapeutic targets to allow individualized clinical management.https://doi.org/10.4137/BBI.S23773 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sylvain Darnet Fabiano C Moreira Igor G Hamoy Rommel Burbano André Khayat Aline Cruz Leandro Magalhães Artur Silva Sidney Santos Samia Demachki Monica Assumpção Paulo Assumpção Âuandrea Ribeiro-Dos-Santos |
spellingShingle |
Sylvain Darnet Fabiano C Moreira Igor G Hamoy Rommel Burbano André Khayat Aline Cruz Leandro Magalhães Artur Silva Sidney Santos Samia Demachki Monica Assumpção Paulo Assumpção Âuandrea Ribeiro-Dos-Santos High-Throughput Sequencing of miRNAs Reveals a Tissue Signature in Gastric Cancer and Suggests Novel Potential Biomarkers Bioinformatics and Biology Insights |
author_facet |
Sylvain Darnet Fabiano C Moreira Igor G Hamoy Rommel Burbano André Khayat Aline Cruz Leandro Magalhães Artur Silva Sidney Santos Samia Demachki Monica Assumpção Paulo Assumpção Âuandrea Ribeiro-Dos-Santos |
author_sort |
Sylvain Darnet |
title |
High-Throughput Sequencing of miRNAs Reveals a Tissue Signature in Gastric Cancer and Suggests Novel Potential Biomarkers |
title_short |
High-Throughput Sequencing of miRNAs Reveals a Tissue Signature in Gastric Cancer and Suggests Novel Potential Biomarkers |
title_full |
High-Throughput Sequencing of miRNAs Reveals a Tissue Signature in Gastric Cancer and Suggests Novel Potential Biomarkers |
title_fullStr |
High-Throughput Sequencing of miRNAs Reveals a Tissue Signature in Gastric Cancer and Suggests Novel Potential Biomarkers |
title_full_unstemmed |
High-Throughput Sequencing of miRNAs Reveals a Tissue Signature in Gastric Cancer and Suggests Novel Potential Biomarkers |
title_sort |
high-throughput sequencing of mirnas reveals a tissue signature in gastric cancer and suggests novel potential biomarkers |
publisher |
SAGE Publishing |
series |
Bioinformatics and Biology Insights |
issn |
1177-9322 |
publishDate |
2015-01-01 |
description |
Gastric cancer has a high incidence and mortality rate worldwide; however, the use of biomarkers for its clinical diagnosis remains limited. The microRNAs (miRNAs) are biomarkers with the potential to identify the risk and prognosis as well as therapeutic targets. We performed the ultradeep miRnomes sequencing of gastric adenocarcinoma and gastric antrum without tumor samples. We observed that a small set of those samples were responsible for approximately 80% of the total miRNAs expression, which might represent a miRNA tissue signature. Additionally, we identified seven miRNAs exhibiting significant differences, and, of these, hsa-miR-135b and hsa-miR-29c were able to discriminate antrum without tumor from gastric cancer regardless of the histological type. These findings were validated by quantitative real-time polymerase chain reaction. The results revealed that hsa-miR-135b and hsa-miR-29c are potential gastric adenocarcinoma occurrence biomarkers with the ability to identify individuals at a higher risk of developing this cancer, and could even be used as therapeutic targets to allow individualized clinical management. |
url |
https://doi.org/10.4137/BBI.S23773 |
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