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Association between circ_0004365 and cisplatin resistance in esophageal squamous cell carcinoma
Cisplatin is one of the most predominant drugs for the chemotherapy of esophageal squamous cell carcinoma (ESCC); however, the underlying resistance mechanisms are still almost unknown. The present study performed RNA sequencing of human circular RNA (circRNA) in TE11 cells and cisplatin-resistant T...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10534278/ https://www.ncbi.nlm.nih.gov/pubmed/37780544 http://dx.doi.org/10.3892/ol.2023.14054 |
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author | Yamada, Moyuru Tanaka, Koji Yamamoto, Kenichi Matsumoto, Hisatake Yamasaki, Makoto Yamashita, Kotaro Makino, Tomoki Saito, Takuro Yamamoto, Kazuyoshi Takahashi, Tsuyoshi Kurokawa, Yukinori Nakajima, Kiyokazu Okada, Yukinori Eguchi, Hidetoshi Doki, Yuichiro |
author_facet | Yamada, Moyuru Tanaka, Koji Yamamoto, Kenichi Matsumoto, Hisatake Yamasaki, Makoto Yamashita, Kotaro Makino, Tomoki Saito, Takuro Yamamoto, Kazuyoshi Takahashi, Tsuyoshi Kurokawa, Yukinori Nakajima, Kiyokazu Okada, Yukinori Eguchi, Hidetoshi Doki, Yuichiro |
author_sort | Yamada, Moyuru |
collection | PubMed |
description | Cisplatin is one of the most predominant drugs for the chemotherapy of esophageal squamous cell carcinoma (ESCC); however, the underlying resistance mechanisms are still almost unknown. The present study performed RNA sequencing of human circular RNA (circRNA) in TE11 cells and cisplatin-resistant TE11 cells (TE11R). The expression profiles determined using CIRCexplorer2 revealed that the expression of circ_0004365, mapped on the Semaphorin 3C gene, was significantly greater in TE11R compared with in TE11. In reverse transcription-quantitative PCR, circ_0004365 expression was observed in human ESCC and non-tumor tissues and was significantly upregulated in ESCC tumor tissues after chemotherapy. Circ_0004365 expression was significantly upregulated in patients with poor pathological response (P=0.02). Furthermore, patients with advanced pT stage showed an upregulation in circ_0004365 expression after chemotherapy (P=0.02). The MTT assay revealed that knockdown of circ_0003465 in TE11 significantly decreased resistance to cisplatin. In conclusion, the present study suggested that circ_0004365 was associated with cisplatin resistance in ESCC and can be used as both a novel biomarker and a therapeutic target. |
format | Online Article Text |
id | pubmed-10534278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-105342782023-09-29 Association between circ_0004365 and cisplatin resistance in esophageal squamous cell carcinoma Yamada, Moyuru Tanaka, Koji Yamamoto, Kenichi Matsumoto, Hisatake Yamasaki, Makoto Yamashita, Kotaro Makino, Tomoki Saito, Takuro Yamamoto, Kazuyoshi Takahashi, Tsuyoshi Kurokawa, Yukinori Nakajima, Kiyokazu Okada, Yukinori Eguchi, Hidetoshi Doki, Yuichiro Oncol Lett Articles Cisplatin is one of the most predominant drugs for the chemotherapy of esophageal squamous cell carcinoma (ESCC); however, the underlying resistance mechanisms are still almost unknown. The present study performed RNA sequencing of human circular RNA (circRNA) in TE11 cells and cisplatin-resistant TE11 cells (TE11R). The expression profiles determined using CIRCexplorer2 revealed that the expression of circ_0004365, mapped on the Semaphorin 3C gene, was significantly greater in TE11R compared with in TE11. In reverse transcription-quantitative PCR, circ_0004365 expression was observed in human ESCC and non-tumor tissues and was significantly upregulated in ESCC tumor tissues after chemotherapy. Circ_0004365 expression was significantly upregulated in patients with poor pathological response (P=0.02). Furthermore, patients with advanced pT stage showed an upregulation in circ_0004365 expression after chemotherapy (P=0.02). The MTT assay revealed that knockdown of circ_0003465 in TE11 significantly decreased resistance to cisplatin. In conclusion, the present study suggested that circ_0004365 was associated with cisplatin resistance in ESCC and can be used as both a novel biomarker and a therapeutic target. D.A. Spandidos 2023-09-18 /pmc/articles/PMC10534278/ /pubmed/37780544 http://dx.doi.org/10.3892/ol.2023.14054 Text en Copyright: © Yamada et al. https://creativecommons.org/licenses/by-nc-nd/4.0/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 Yamada, Moyuru Tanaka, Koji Yamamoto, Kenichi Matsumoto, Hisatake Yamasaki, Makoto Yamashita, Kotaro Makino, Tomoki Saito, Takuro Yamamoto, Kazuyoshi Takahashi, Tsuyoshi Kurokawa, Yukinori Nakajima, Kiyokazu Okada, Yukinori Eguchi, Hidetoshi Doki, Yuichiro Association between circ_0004365 and cisplatin resistance in esophageal squamous cell carcinoma |
title | Association between circ_0004365 and cisplatin resistance in esophageal squamous cell carcinoma |
title_full | Association between circ_0004365 and cisplatin resistance in esophageal squamous cell carcinoma |
title_fullStr | Association between circ_0004365 and cisplatin resistance in esophageal squamous cell carcinoma |
title_full_unstemmed | Association between circ_0004365 and cisplatin resistance in esophageal squamous cell carcinoma |
title_short | Association between circ_0004365 and cisplatin resistance in esophageal squamous cell carcinoma |
title_sort | association between circ_0004365 and cisplatin resistance in esophageal squamous cell carcinoma |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10534278/ https://www.ncbi.nlm.nih.gov/pubmed/37780544 http://dx.doi.org/10.3892/ol.2023.14054 |
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