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Dysregulated miRNA in a cancer-prone environment: A study of gastric non-neoplastic mucosa
Understanding cancer-prone environments is important to efficiently detect and prevent cancers. The associations between miRNA and cancer-prone environments are still largely unknown in gastric cancer (GC). Six miRNAs that are differentially expressed during gastric carcinogenesis were selected, and...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171080/ https://www.ncbi.nlm.nih.gov/pubmed/32313120 http://dx.doi.org/10.1038/s41598-020-63230-1 |
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author | Kim, Binnari Jang, Jiryeon Heo, You Jeong Kang, So Young Yoo, Heejin Sohn, Insuk Min, Byung-Hoon Kim, Kyoung-Mee |
author_facet | Kim, Binnari Jang, Jiryeon Heo, You Jeong Kang, So Young Yoo, Heejin Sohn, Insuk Min, Byung-Hoon Kim, Kyoung-Mee |
author_sort | Kim, Binnari |
collection | PubMed |
description | Understanding cancer-prone environments is important to efficiently detect and prevent cancers. The associations between miRNA and cancer-prone environments are still largely unknown in gastric cancer (GC). Six miRNAs that are differentially expressed during gastric carcinogenesis were selected, and quantitative real-time PCR was performed in an independent training set (fresh non-tumor and tumor samples from 18 GC patients) and validation sets (set 1 with formalin-fixed paraffin-embedded non-tumor and tumor samples from 19 solitary GC and set 2 with 37 multiple GC patients). The results were compared with those of 37 gastric mucosa from 20 healthy volunteers. The expression levels of miR-26a, miR-375, and miR-1260 in gastric mucosa from healthy volunteers were statistically higher than that of non-tumorous gastric mucosa located 3 cm apart from the GC in the training set (miR-26a, P < 0.0001; miR-375, P = 0.0049; miR-1260, P = 0.0172), validation set 1 (miR-26a and miR-375, P < 0.0001; miR-1260, P = 0.0008), and validation set 2 (miR-26a, miR-375, and miR-1260, P < 0.0001). And a combination of miR-26a and miR-1260 showed the highest area under the curve value of 0.89. miRNAs are differentially expressed in non-neoplastic gastric mucosa and can be used as a biomarker to predict cancer-prone environments. |
format | Online Article Text |
id | pubmed-7171080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71710802020-04-23 Dysregulated miRNA in a cancer-prone environment: A study of gastric non-neoplastic mucosa Kim, Binnari Jang, Jiryeon Heo, You Jeong Kang, So Young Yoo, Heejin Sohn, Insuk Min, Byung-Hoon Kim, Kyoung-Mee Sci Rep Article Understanding cancer-prone environments is important to efficiently detect and prevent cancers. The associations between miRNA and cancer-prone environments are still largely unknown in gastric cancer (GC). Six miRNAs that are differentially expressed during gastric carcinogenesis were selected, and quantitative real-time PCR was performed in an independent training set (fresh non-tumor and tumor samples from 18 GC patients) and validation sets (set 1 with formalin-fixed paraffin-embedded non-tumor and tumor samples from 19 solitary GC and set 2 with 37 multiple GC patients). The results were compared with those of 37 gastric mucosa from 20 healthy volunteers. The expression levels of miR-26a, miR-375, and miR-1260 in gastric mucosa from healthy volunteers were statistically higher than that of non-tumorous gastric mucosa located 3 cm apart from the GC in the training set (miR-26a, P < 0.0001; miR-375, P = 0.0049; miR-1260, P = 0.0172), validation set 1 (miR-26a and miR-375, P < 0.0001; miR-1260, P = 0.0008), and validation set 2 (miR-26a, miR-375, and miR-1260, P < 0.0001). And a combination of miR-26a and miR-1260 showed the highest area under the curve value of 0.89. miRNAs are differentially expressed in non-neoplastic gastric mucosa and can be used as a biomarker to predict cancer-prone environments. Nature Publishing Group UK 2020-04-20 /pmc/articles/PMC7171080/ /pubmed/32313120 http://dx.doi.org/10.1038/s41598-020-63230-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kim, Binnari Jang, Jiryeon Heo, You Jeong Kang, So Young Yoo, Heejin Sohn, Insuk Min, Byung-Hoon Kim, Kyoung-Mee Dysregulated miRNA in a cancer-prone environment: A study of gastric non-neoplastic mucosa |
title | Dysregulated miRNA in a cancer-prone environment: A study of gastric non-neoplastic mucosa |
title_full | Dysregulated miRNA in a cancer-prone environment: A study of gastric non-neoplastic mucosa |
title_fullStr | Dysregulated miRNA in a cancer-prone environment: A study of gastric non-neoplastic mucosa |
title_full_unstemmed | Dysregulated miRNA in a cancer-prone environment: A study of gastric non-neoplastic mucosa |
title_short | Dysregulated miRNA in a cancer-prone environment: A study of gastric non-neoplastic mucosa |
title_sort | dysregulated mirna in a cancer-prone environment: a study of gastric non-neoplastic mucosa |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171080/ https://www.ncbi.nlm.nih.gov/pubmed/32313120 http://dx.doi.org/10.1038/s41598-020-63230-1 |
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