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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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Published in: | Bioinformatics and biology insights 2015-06, Vol.9 (Suppl 1), p.1-8 |
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creator | Darnet, Sylvain Moreira, Fabiano C Hamoy, Igor G Burbano, Rommel Khayat, André Cruz, Aline Magalhães, Leandro Silva, Artur Santos, Sidney Demachki, Samia Assumpção, Monica Assumpção, Paulo Ribeiro-dos-Santos, Ândrea |
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. |
doi_str_mv | 10.4137/BBI.S23773 |
format | article |
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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.</description><identifier>EISSN: 1177-9322</identifier><identifier>DOI: 10.4137/BBI.S23773</identifier><identifier>PMID: 25698879</identifier><identifier>PMID: 26157332</identifier><language>eng</language><publisher>Libertas Academica</publisher><subject>Original Research</subject><ispartof>Bioinformatics and biology insights, 2015-06, Vol.9 (Suppl 1), p.1-8</ispartof><rights>2015 the authors, publisher and licensee Libertas Academica Limited. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4485834/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4485834/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids></links><search><creatorcontrib>Darnet, Sylvain</creatorcontrib><creatorcontrib>Moreira, Fabiano C</creatorcontrib><creatorcontrib>Hamoy, Igor G</creatorcontrib><creatorcontrib>Burbano, Rommel</creatorcontrib><creatorcontrib>Khayat, André</creatorcontrib><creatorcontrib>Cruz, Aline</creatorcontrib><creatorcontrib>Magalhães, Leandro</creatorcontrib><creatorcontrib>Silva, Artur</creatorcontrib><creatorcontrib>Santos, Sidney</creatorcontrib><creatorcontrib>Demachki, Samia</creatorcontrib><creatorcontrib>Assumpção, Monica</creatorcontrib><creatorcontrib>Assumpção, Paulo</creatorcontrib><creatorcontrib>Ribeiro-dos-Santos, Ândrea</creatorcontrib><title>High-Throughput Sequencing of miRNAs Reveals a Tissue Signature in Gastric Cancer and Suggests Novel Potential Biomarkers</title><title>Bioinformatics and biology insights</title><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
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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.</abstract><pub>Libertas Academica</pub><pmid>25698879</pmid><pmid>26157332</pmid><doi>10.4137/BBI.S23773</doi><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | SAGE Open Access; Publicly Available Content (ProQuest); PubMed Central |
subjects | Original Research |
title | High-Throughput Sequencing of miRNAs Reveals a Tissue Signature in Gastric Cancer and Suggests Novel Potential Biomarkers |
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