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Circulating plasma microRNAs in colorectal neoplasia: A pilot study in assessing response to therapy

INTRODUCTION: Current serological surveillance markers to monitor colorectal cancer (CRC) or colorectal advanced adenomas (CAA) are hampered by poor sensitivity and specificity. The aim of this study is to identify and validate a panel of plasma microRNAs which change in expression after resection o...

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Autores principales: O'Brien, Stephen J, Netz, Uri, Hallion, Jacob, Bishop, Campbell, Stephen, Vincent, Burton, James, Paas, Mason, Feagins, Kayla, Pan, Jianmin, Rai, Shesh N., Galandiuk, Susan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Neoplasia Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720092/
https://www.ncbi.nlm.nih.gov/pubmed/33285367
http://dx.doi.org/10.1016/j.tranon.2020.100962
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author O'Brien, Stephen J
Netz, Uri
Hallion, Jacob
Bishop, Campbell
Stephen, Vincent
Burton, James
Paas, Mason
Feagins, Kayla
Pan, Jianmin
Rai, Shesh N.
Galandiuk, Susan
author_facet O'Brien, Stephen J
Netz, Uri
Hallion, Jacob
Bishop, Campbell
Stephen, Vincent
Burton, James
Paas, Mason
Feagins, Kayla
Pan, Jianmin
Rai, Shesh N.
Galandiuk, Susan
author_sort O'Brien, Stephen J
collection PubMed
description INTRODUCTION: Current serological surveillance markers to monitor colorectal cancer (CRC) or colorectal advanced adenomas (CAA) are hampered by poor sensitivity and specificity. The aim of this study is to identify and validate a panel of plasma microRNAs which change in expression after resection of such lesions. METHODS: A prospectively maintained colorectal surgery database was queried for patients in whom both pre- and post-procedural serum samples had been obtained. An initial screening analysis of CRC and CAA patients (5 each) was conducted using screening cards for 380 miRNAs. Four identified miRNAs were combined with a previously described panel of 7 miRNAs that were diagnostically predictive of CRC and CAA. Differential miRNA expression was assessed using quantitative real-time polymerase chain reaction(qRT-PCR). RESULTS: Fifty patients were included (n = 27 CRC, n = 23 CAA). There was no difference in age, gender, or race profile of CRC patients compared to CAA patients. Six miRNA were significantly increased after CRC resection (miR-324, let7b, miR-454, miR-374a, miR-122, miR-19b, all p<0.05), while three miRNAs were significantly increased following CAA resection (miR-454, miR-374a, miR-122, all p<0.05). Three miRNA were increased in common for both (miR-454, miR-374a, miR-122). DISCUSSION: The expression of miRNAs associated with neoplasia (either CRC or CAA) was significantly increased following surgical resection or endoscopic removal of CRC or CAA. Future studies should focus on the evaluation of these miRNAs in CRC and CAA prognosis.
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spelling pubmed-77200922020-12-15 Circulating plasma microRNAs in colorectal neoplasia: A pilot study in assessing response to therapy O'Brien, Stephen J Netz, Uri Hallion, Jacob Bishop, Campbell Stephen, Vincent Burton, James Paas, Mason Feagins, Kayla Pan, Jianmin Rai, Shesh N. Galandiuk, Susan Transl Oncol Original article INTRODUCTION: Current serological surveillance markers to monitor colorectal cancer (CRC) or colorectal advanced adenomas (CAA) are hampered by poor sensitivity and specificity. The aim of this study is to identify and validate a panel of plasma microRNAs which change in expression after resection of such lesions. METHODS: A prospectively maintained colorectal surgery database was queried for patients in whom both pre- and post-procedural serum samples had been obtained. An initial screening analysis of CRC and CAA patients (5 each) was conducted using screening cards for 380 miRNAs. Four identified miRNAs were combined with a previously described panel of 7 miRNAs that were diagnostically predictive of CRC and CAA. Differential miRNA expression was assessed using quantitative real-time polymerase chain reaction(qRT-PCR). RESULTS: Fifty patients were included (n = 27 CRC, n = 23 CAA). There was no difference in age, gender, or race profile of CRC patients compared to CAA patients. Six miRNA were significantly increased after CRC resection (miR-324, let7b, miR-454, miR-374a, miR-122, miR-19b, all p<0.05), while three miRNAs were significantly increased following CAA resection (miR-454, miR-374a, miR-122, all p<0.05). Three miRNA were increased in common for both (miR-454, miR-374a, miR-122). DISCUSSION: The expression of miRNAs associated with neoplasia (either CRC or CAA) was significantly increased following surgical resection or endoscopic removal of CRC or CAA. Future studies should focus on the evaluation of these miRNAs in CRC and CAA prognosis. Neoplasia Press 2020-12-04 /pmc/articles/PMC7720092/ /pubmed/33285367 http://dx.doi.org/10.1016/j.tranon.2020.100962 Text en © 2020 Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original article
O'Brien, Stephen J
Netz, Uri
Hallion, Jacob
Bishop, Campbell
Stephen, Vincent
Burton, James
Paas, Mason
Feagins, Kayla
Pan, Jianmin
Rai, Shesh N.
Galandiuk, Susan
Circulating plasma microRNAs in colorectal neoplasia: A pilot study in assessing response to therapy
title Circulating plasma microRNAs in colorectal neoplasia: A pilot study in assessing response to therapy
title_full Circulating plasma microRNAs in colorectal neoplasia: A pilot study in assessing response to therapy
title_fullStr Circulating plasma microRNAs in colorectal neoplasia: A pilot study in assessing response to therapy
title_full_unstemmed Circulating plasma microRNAs in colorectal neoplasia: A pilot study in assessing response to therapy
title_short Circulating plasma microRNAs in colorectal neoplasia: A pilot study in assessing response to therapy
title_sort circulating plasma micrornas in colorectal neoplasia: a pilot study in assessing response to therapy
topic Original article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720092/
https://www.ncbi.nlm.nih.gov/pubmed/33285367
http://dx.doi.org/10.1016/j.tranon.2020.100962
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