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Serum levels of candidate microRNA diagnostic markers differ among the stages of non-small-cell lung cancer

Circulating microRNAs (miRNAs) are promising markers for cancer diagnosis and prognosis. Numerous studies evaluating miRNAs as markers for non-small cell lung cancer (NSCLC) have been conducted in recent years; however, the majority of candidate markers proposed via individual studies were inconsist...

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Autores principales: Aiso, Toshiko, Ohtsuka, Kouki, Ueda, Makiko, Karita, Shin, Yokoyama, Takuma, Takata, Saori, Matsuki, Naoko, Kondo, Haruhiko, Takizawa, Hajime, Okada, Annabelle A., Watanabe, Takashi, Ohnishi, Hiroaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202492/
https://www.ncbi.nlm.nih.gov/pubmed/30405804
http://dx.doi.org/10.3892/ol.2018.9464
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author Aiso, Toshiko
Ohtsuka, Kouki
Ueda, Makiko
Karita, Shin
Yokoyama, Takuma
Takata, Saori
Matsuki, Naoko
Kondo, Haruhiko
Takizawa, Hajime
Okada, Annabelle A.
Watanabe, Takashi
Ohnishi, Hiroaki
author_facet Aiso, Toshiko
Ohtsuka, Kouki
Ueda, Makiko
Karita, Shin
Yokoyama, Takuma
Takata, Saori
Matsuki, Naoko
Kondo, Haruhiko
Takizawa, Hajime
Okada, Annabelle A.
Watanabe, Takashi
Ohnishi, Hiroaki
author_sort Aiso, Toshiko
collection PubMed
description Circulating microRNAs (miRNAs) are promising markers for cancer diagnosis and prognosis. Numerous studies evaluating miRNAs as markers for non-small cell lung cancer (NSCLC) have been conducted in recent years; however, the majority of candidate markers proposed via individual studies were inconsistent and no marker miRNAs for the diagnosis of early stage NSCLC have been established. In the present study, miR-145, miR-20a, miR-21 and miR-223, which were previously reported as candidate diagnostic markers of NSCLC, were re-evaluated. The serum levels of these miRNAs were quantified in 56 patients with stage I–IV NSCLC using the TaqMan microRNA assays and separately compared the levels at each stage with those in 26 control patients. The level of miR-145 was significantly reduced in patients with NSCLC, regardless of clinical stage, and its level increased following tumor resection in patients with stage I–II disease. These results indicate that miR-145 is relevant as a diagnostic marker for stages I–IV NSCLC. Additionally, the levels of miR-20a and miR-21 demonstrated notable differences among patients at different clinical stages. These miRNAs distinguished patients in a number of, but not all, stages of NSCLC from cancer-free control patients. These results indicated that it is essential to analyze miRNA levels at each stage separately in order to evaluate marker miRNAs for NSCLC diagnosis.
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spelling pubmed-62024922018-11-07 Serum levels of candidate microRNA diagnostic markers differ among the stages of non-small-cell lung cancer Aiso, Toshiko Ohtsuka, Kouki Ueda, Makiko Karita, Shin Yokoyama, Takuma Takata, Saori Matsuki, Naoko Kondo, Haruhiko Takizawa, Hajime Okada, Annabelle A. Watanabe, Takashi Ohnishi, Hiroaki Oncol Lett Articles Circulating microRNAs (miRNAs) are promising markers for cancer diagnosis and prognosis. Numerous studies evaluating miRNAs as markers for non-small cell lung cancer (NSCLC) have been conducted in recent years; however, the majority of candidate markers proposed via individual studies were inconsistent and no marker miRNAs for the diagnosis of early stage NSCLC have been established. In the present study, miR-145, miR-20a, miR-21 and miR-223, which were previously reported as candidate diagnostic markers of NSCLC, were re-evaluated. The serum levels of these miRNAs were quantified in 56 patients with stage I–IV NSCLC using the TaqMan microRNA assays and separately compared the levels at each stage with those in 26 control patients. The level of miR-145 was significantly reduced in patients with NSCLC, regardless of clinical stage, and its level increased following tumor resection in patients with stage I–II disease. These results indicate that miR-145 is relevant as a diagnostic marker for stages I–IV NSCLC. Additionally, the levels of miR-20a and miR-21 demonstrated notable differences among patients at different clinical stages. These miRNAs distinguished patients in a number of, but not all, stages of NSCLC from cancer-free control patients. These results indicated that it is essential to analyze miRNA levels at each stage separately in order to evaluate marker miRNAs for NSCLC diagnosis. D.A. Spandidos 2018-11 2018-09-20 /pmc/articles/PMC6202492/ /pubmed/30405804 http://dx.doi.org/10.3892/ol.2018.9464 Text en Copyright: © Aiso et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Aiso, Toshiko
Ohtsuka, Kouki
Ueda, Makiko
Karita, Shin
Yokoyama, Takuma
Takata, Saori
Matsuki, Naoko
Kondo, Haruhiko
Takizawa, Hajime
Okada, Annabelle A.
Watanabe, Takashi
Ohnishi, Hiroaki
Serum levels of candidate microRNA diagnostic markers differ among the stages of non-small-cell lung cancer
title Serum levels of candidate microRNA diagnostic markers differ among the stages of non-small-cell lung cancer
title_full Serum levels of candidate microRNA diagnostic markers differ among the stages of non-small-cell lung cancer
title_fullStr Serum levels of candidate microRNA diagnostic markers differ among the stages of non-small-cell lung cancer
title_full_unstemmed Serum levels of candidate microRNA diagnostic markers differ among the stages of non-small-cell lung cancer
title_short Serum levels of candidate microRNA diagnostic markers differ among the stages of non-small-cell lung cancer
title_sort serum levels of candidate microrna diagnostic markers differ among the stages of non-small-cell lung cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202492/
https://www.ncbi.nlm.nih.gov/pubmed/30405804
http://dx.doi.org/10.3892/ol.2018.9464
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