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Serum miR-143 levels predict the pathological response to neoadjuvant chemoradiotherapy in patients with locally advanced rectal cancer

Recently, several circulating miRNAs have been reported as promising, minimally invasive biomarkers for the diagnosis or prediction of the prognosis in various types of cancer. However, the utility of circulating miRNAs as predictive markers of the cancer response to neoadjuvant chemoradiotherapy (n...

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Autores principales: Hiyoshi, Yukiharu, Akiyoshi, Takashi, Inoue, Ramu, Murofushi, Keiko, Yamamoto, Noriko, Fukunaga, Yosuke, Ueno, Masashi, Baba, Hideo, Mori, Seiichi, Yamaguchi, Toshiharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5668032/
https://www.ncbi.nlm.nih.gov/pubmed/29108299
http://dx.doi.org/10.18632/oncotarget.16760
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author Hiyoshi, Yukiharu
Akiyoshi, Takashi
Inoue, Ramu
Murofushi, Keiko
Yamamoto, Noriko
Fukunaga, Yosuke
Ueno, Masashi
Baba, Hideo
Mori, Seiichi
Yamaguchi, Toshiharu
author_facet Hiyoshi, Yukiharu
Akiyoshi, Takashi
Inoue, Ramu
Murofushi, Keiko
Yamamoto, Noriko
Fukunaga, Yosuke
Ueno, Masashi
Baba, Hideo
Mori, Seiichi
Yamaguchi, Toshiharu
author_sort Hiyoshi, Yukiharu
collection PubMed
description Recently, several circulating miRNAs have been reported as promising, minimally invasive biomarkers for the diagnosis or prediction of the prognosis in various types of cancer. However, the utility of circulating miRNAs as predictive markers of the cancer response to neoadjuvant chemoradiotherapy (nCRT) for locally advanced rectal cancer is still unclear. To identify circulating serum miRNAs useful for predicting a pathological good response to nCRT, total 18 serum miRNAs of interest were analyzed by real-time polymerase chain reaction in 94 rectal cancer patients treated with nCRT and surgery. Pathological complete response (pCR; Dworak TRG4) and near-pCR (TRG3) were obtained in 12 (13%) and 9 (9%) patients respectively, and we regarded them as nCRT-responders. Of the 18 serum miRNAs, only the serum level of miR-143 was identified significantly associated with a pathological response to nCRT in 94 patients; the serum miR-143 level was significantly lower in nCRT-responders than in non-responders. A multivariate analysis incorporating other clinicopathological factors showed that only the serum miR-143 level was an independent predictor of a good pathological response. The circulating serum miR-143 level may be a novel, non-invasive predictive marker of a response to nCRT in locally advanced rectal cancer patients.
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spelling pubmed-56680322017-11-04 Serum miR-143 levels predict the pathological response to neoadjuvant chemoradiotherapy in patients with locally advanced rectal cancer Hiyoshi, Yukiharu Akiyoshi, Takashi Inoue, Ramu Murofushi, Keiko Yamamoto, Noriko Fukunaga, Yosuke Ueno, Masashi Baba, Hideo Mori, Seiichi Yamaguchi, Toshiharu Oncotarget Clinical Research Paper Recently, several circulating miRNAs have been reported as promising, minimally invasive biomarkers for the diagnosis or prediction of the prognosis in various types of cancer. However, the utility of circulating miRNAs as predictive markers of the cancer response to neoadjuvant chemoradiotherapy (nCRT) for locally advanced rectal cancer is still unclear. To identify circulating serum miRNAs useful for predicting a pathological good response to nCRT, total 18 serum miRNAs of interest were analyzed by real-time polymerase chain reaction in 94 rectal cancer patients treated with nCRT and surgery. Pathological complete response (pCR; Dworak TRG4) and near-pCR (TRG3) were obtained in 12 (13%) and 9 (9%) patients respectively, and we regarded them as nCRT-responders. Of the 18 serum miRNAs, only the serum level of miR-143 was identified significantly associated with a pathological response to nCRT in 94 patients; the serum miR-143 level was significantly lower in nCRT-responders than in non-responders. A multivariate analysis incorporating other clinicopathological factors showed that only the serum miR-143 level was an independent predictor of a good pathological response. The circulating serum miR-143 level may be a novel, non-invasive predictive marker of a response to nCRT in locally advanced rectal cancer patients. Impact Journals LLC 2017-03-31 /pmc/articles/PMC5668032/ /pubmed/29108299 http://dx.doi.org/10.18632/oncotarget.16760 Text en Copyright: © 2017 Hiyoshi et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Clinical Research Paper
Hiyoshi, Yukiharu
Akiyoshi, Takashi
Inoue, Ramu
Murofushi, Keiko
Yamamoto, Noriko
Fukunaga, Yosuke
Ueno, Masashi
Baba, Hideo
Mori, Seiichi
Yamaguchi, Toshiharu
Serum miR-143 levels predict the pathological response to neoadjuvant chemoradiotherapy in patients with locally advanced rectal cancer
title Serum miR-143 levels predict the pathological response to neoadjuvant chemoradiotherapy in patients with locally advanced rectal cancer
title_full Serum miR-143 levels predict the pathological response to neoadjuvant chemoradiotherapy in patients with locally advanced rectal cancer
title_fullStr Serum miR-143 levels predict the pathological response to neoadjuvant chemoradiotherapy in patients with locally advanced rectal cancer
title_full_unstemmed Serum miR-143 levels predict the pathological response to neoadjuvant chemoradiotherapy in patients with locally advanced rectal cancer
title_short Serum miR-143 levels predict the pathological response to neoadjuvant chemoradiotherapy in patients with locally advanced rectal cancer
title_sort serum mir-143 levels predict the pathological response to neoadjuvant chemoradiotherapy in patients with locally advanced rectal cancer
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5668032/
https://www.ncbi.nlm.nih.gov/pubmed/29108299
http://dx.doi.org/10.18632/oncotarget.16760
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