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Plasma microRNA‐192‐5p can predict the response to neoadjuvant chemotherapy and prognosis in esophageal cancer

Esophageal cancer (EC) is the sixth leading cause of cancer‐related death worldwide. Recently, neoadjuvant chemotherapy (NAC) before curative surgery has become a standard treatment for clinical stage II or III EC patients. Some EC patients receive a complete response (CR) by NAC; thus, curative sur...

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Autores principales: Furuke, Hirotaka, Konishi, Hirotaka, Arita, Tomohiro, Kataoka, Satoshi, Shibamoto, Jun, Takabatake, Kazuya, Takaki, Wataru, Shimizu, Hiroki, Yamamoto, Yusuke, Komatsu, Shuhei, Shiozaki, Atsushi, Fujiwara, Hitoshi, Otsuji, Eigo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067423/
https://www.ncbi.nlm.nih.gov/pubmed/36533956
http://dx.doi.org/10.1111/cas.15703
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author Furuke, Hirotaka
Konishi, Hirotaka
Arita, Tomohiro
Kataoka, Satoshi
Shibamoto, Jun
Takabatake, Kazuya
Takaki, Wataru
Shimizu, Hiroki
Yamamoto, Yusuke
Komatsu, Shuhei
Shiozaki, Atsushi
Fujiwara, Hitoshi
Otsuji, Eigo
author_facet Furuke, Hirotaka
Konishi, Hirotaka
Arita, Tomohiro
Kataoka, Satoshi
Shibamoto, Jun
Takabatake, Kazuya
Takaki, Wataru
Shimizu, Hiroki
Yamamoto, Yusuke
Komatsu, Shuhei
Shiozaki, Atsushi
Fujiwara, Hitoshi
Otsuji, Eigo
author_sort Furuke, Hirotaka
collection PubMed
description Esophageal cancer (EC) is the sixth leading cause of cancer‐related death worldwide. Recently, neoadjuvant chemotherapy (NAC) before curative surgery has become a standard treatment for clinical stage II or III EC patients. Some EC patients receive a complete response (CR) by NAC; thus, curative surgery may be unnecessary for such patients. MicroRNA levels in plasma have the potential to be a predictor of response to NAC. In the present study, we focused on miR‐192‐5p, which is highly expressed in EC tissue. The purpose was to investigate the correlations between levels of plasma miR‐192‐5p and the response to NAC. Furthermore, molecular functions of miR‐192‐5p associated with chemosensitivity were examined using EC cell lines. The levels of miR‐192‐5p in plasma before surgery were evaluated in 113 EC patients. Sixty‐nine patients received NAC. miR‐192‐5p levels in the CR group were significantly higher than in the other groups (p = 0.002). The downregulation of miR‐192‐5p in the EC cell line inhibited sensitivity to cisplatin, and the overexpression of miR‐192‐5p in the EC cell line promoted sensitivity to cisplatin. miR‐192‐5p regulated sensitivity to cisplatin by targeting ERCC3 and ERCC4. Plasma miR‐192‐5p could be used as a predictor of response to chemotherapy and prognosis in EC patients.
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spelling pubmed-100674232023-04-04 Plasma microRNA‐192‐5p can predict the response to neoadjuvant chemotherapy and prognosis in esophageal cancer Furuke, Hirotaka Konishi, Hirotaka Arita, Tomohiro Kataoka, Satoshi Shibamoto, Jun Takabatake, Kazuya Takaki, Wataru Shimizu, Hiroki Yamamoto, Yusuke Komatsu, Shuhei Shiozaki, Atsushi Fujiwara, Hitoshi Otsuji, Eigo Cancer Sci ORIGINAL ARTICLES Esophageal cancer (EC) is the sixth leading cause of cancer‐related death worldwide. Recently, neoadjuvant chemotherapy (NAC) before curative surgery has become a standard treatment for clinical stage II or III EC patients. Some EC patients receive a complete response (CR) by NAC; thus, curative surgery may be unnecessary for such patients. MicroRNA levels in plasma have the potential to be a predictor of response to NAC. In the present study, we focused on miR‐192‐5p, which is highly expressed in EC tissue. The purpose was to investigate the correlations between levels of plasma miR‐192‐5p and the response to NAC. Furthermore, molecular functions of miR‐192‐5p associated with chemosensitivity were examined using EC cell lines. The levels of miR‐192‐5p in plasma before surgery were evaluated in 113 EC patients. Sixty‐nine patients received NAC. miR‐192‐5p levels in the CR group were significantly higher than in the other groups (p = 0.002). The downregulation of miR‐192‐5p in the EC cell line inhibited sensitivity to cisplatin, and the overexpression of miR‐192‐5p in the EC cell line promoted sensitivity to cisplatin. miR‐192‐5p regulated sensitivity to cisplatin by targeting ERCC3 and ERCC4. Plasma miR‐192‐5p could be used as a predictor of response to chemotherapy and prognosis in EC patients. John Wiley and Sons Inc. 2022-12-26 /pmc/articles/PMC10067423/ /pubmed/36533956 http://dx.doi.org/10.1111/cas.15703 Text en © 2022 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle ORIGINAL ARTICLES
Furuke, Hirotaka
Konishi, Hirotaka
Arita, Tomohiro
Kataoka, Satoshi
Shibamoto, Jun
Takabatake, Kazuya
Takaki, Wataru
Shimizu, Hiroki
Yamamoto, Yusuke
Komatsu, Shuhei
Shiozaki, Atsushi
Fujiwara, Hitoshi
Otsuji, Eigo
Plasma microRNA‐192‐5p can predict the response to neoadjuvant chemotherapy and prognosis in esophageal cancer
title Plasma microRNA‐192‐5p can predict the response to neoadjuvant chemotherapy and prognosis in esophageal cancer
title_full Plasma microRNA‐192‐5p can predict the response to neoadjuvant chemotherapy and prognosis in esophageal cancer
title_fullStr Plasma microRNA‐192‐5p can predict the response to neoadjuvant chemotherapy and prognosis in esophageal cancer
title_full_unstemmed Plasma microRNA‐192‐5p can predict the response to neoadjuvant chemotherapy and prognosis in esophageal cancer
title_short Plasma microRNA‐192‐5p can predict the response to neoadjuvant chemotherapy and prognosis in esophageal cancer
title_sort plasma microrna‐192‐5p can predict the response to neoadjuvant chemotherapy and prognosis in esophageal cancer
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067423/
https://www.ncbi.nlm.nih.gov/pubmed/36533956
http://dx.doi.org/10.1111/cas.15703
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