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Non-invasive Potential Circulating mRNA Markers for Colorectal Adenoma Using Targeted Sequencing

We have developed an optimized protocol for plasma targeted mRNA sequencing in our previous study. Here, we performed plasma targeted mRNA sequencing for 40 colorectal adenoma patients and 39 colonoscopy-proven normal controls in order to find potential circulating mRNA markers for colorectal adenom...

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Autores principales: Xue, Vivian W., Cheung, Moon T., Chan, Pak T., Luk, Lewis L. Y., Lee, Vivian H., Au, Thomas C., Yu, Allen C., Cho, William C. S., Tsang, Hin Fung Andy, Chan, Amanda K., Wong, S. C. Cesar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6736954/
https://www.ncbi.nlm.nih.gov/pubmed/31506480
http://dx.doi.org/10.1038/s41598-019-49445-x
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author Xue, Vivian W.
Cheung, Moon T.
Chan, Pak T.
Luk, Lewis L. Y.
Lee, Vivian H.
Au, Thomas C.
Yu, Allen C.
Cho, William C. S.
Tsang, Hin Fung Andy
Chan, Amanda K.
Wong, S. C. Cesar
author_facet Xue, Vivian W.
Cheung, Moon T.
Chan, Pak T.
Luk, Lewis L. Y.
Lee, Vivian H.
Au, Thomas C.
Yu, Allen C.
Cho, William C. S.
Tsang, Hin Fung Andy
Chan, Amanda K.
Wong, S. C. Cesar
author_sort Xue, Vivian W.
collection PubMed
description We have developed an optimized protocol for plasma targeted mRNA sequencing in our previous study. Here, we performed plasma targeted mRNA sequencing for 40 colorectal adenoma patients and 39 colonoscopy-proven normal controls in order to find potential circulating mRNA markers for colorectal adenoma. Results showed that GSK3A and RHOA were differential expressed genes identified by a cut-off of fold change >2 and adjusted P value < 0.05. More detailed analysis showed that the expression of both GSK3A (0.01-fold with adjusted P < 1 × 10(−6)) and RHOA (0.35-fold with adjusted P < 0.01) in adenoma patients was significantly lower than those in normal healthy subjects. Based on the enrichment analysis of biological process for potential markers, we found that the regulation of programmed cell death (GO: 0043067; GO: 0043069), regulation of cell death (GO: 0010941; GO: 0060548) and cell differentiation (GO: 0021861) were the main processes involved in adenoma formation. In summary, this study is a cutting-edge research on the detection of plasma mRNA in colorectal adenoma patients and normal healthy subjects.
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spelling pubmed-67369542019-09-20 Non-invasive Potential Circulating mRNA Markers for Colorectal Adenoma Using Targeted Sequencing Xue, Vivian W. Cheung, Moon T. Chan, Pak T. Luk, Lewis L. Y. Lee, Vivian H. Au, Thomas C. Yu, Allen C. Cho, William C. S. Tsang, Hin Fung Andy Chan, Amanda K. Wong, S. C. Cesar Sci Rep Article We have developed an optimized protocol for plasma targeted mRNA sequencing in our previous study. Here, we performed plasma targeted mRNA sequencing for 40 colorectal adenoma patients and 39 colonoscopy-proven normal controls in order to find potential circulating mRNA markers for colorectal adenoma. Results showed that GSK3A and RHOA were differential expressed genes identified by a cut-off of fold change >2 and adjusted P value < 0.05. More detailed analysis showed that the expression of both GSK3A (0.01-fold with adjusted P < 1 × 10(−6)) and RHOA (0.35-fold with adjusted P < 0.01) in adenoma patients was significantly lower than those in normal healthy subjects. Based on the enrichment analysis of biological process for potential markers, we found that the regulation of programmed cell death (GO: 0043067; GO: 0043069), regulation of cell death (GO: 0010941; GO: 0060548) and cell differentiation (GO: 0021861) were the main processes involved in adenoma formation. In summary, this study is a cutting-edge research on the detection of plasma mRNA in colorectal adenoma patients and normal healthy subjects. Nature Publishing Group UK 2019-09-10 /pmc/articles/PMC6736954/ /pubmed/31506480 http://dx.doi.org/10.1038/s41598-019-49445-x Text en © The Author(s) 2019 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
Xue, Vivian W.
Cheung, Moon T.
Chan, Pak T.
Luk, Lewis L. Y.
Lee, Vivian H.
Au, Thomas C.
Yu, Allen C.
Cho, William C. S.
Tsang, Hin Fung Andy
Chan, Amanda K.
Wong, S. C. Cesar
Non-invasive Potential Circulating mRNA Markers for Colorectal Adenoma Using Targeted Sequencing
title Non-invasive Potential Circulating mRNA Markers for Colorectal Adenoma Using Targeted Sequencing
title_full Non-invasive Potential Circulating mRNA Markers for Colorectal Adenoma Using Targeted Sequencing
title_fullStr Non-invasive Potential Circulating mRNA Markers for Colorectal Adenoma Using Targeted Sequencing
title_full_unstemmed Non-invasive Potential Circulating mRNA Markers for Colorectal Adenoma Using Targeted Sequencing
title_short Non-invasive Potential Circulating mRNA Markers for Colorectal Adenoma Using Targeted Sequencing
title_sort non-invasive potential circulating mrna markers for colorectal adenoma using targeted sequencing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6736954/
https://www.ncbi.nlm.nih.gov/pubmed/31506480
http://dx.doi.org/10.1038/s41598-019-49445-x
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