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Long non‐coding RNA H19 promotes TDRG1 expression and cisplatin resistance by sequestering miRNA‐106b‐5p in seminoma

The role of TDRG1 in tumorigenesis and the progression of seminoma, as well as its role in regulating chemosensitivity of seminoma to cisplatin through the PI3K/Akt/mTOR signaling pathway, has been previously defined. However, the detailed mechanism underlying TDRG1 expression and concomitant chemor...

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Autores principales: Wei, Jingchao, Gan, Yu, Peng, Dongyi, Jiang, Xianzhen, Kitazawa, Riko, Xiang, Yali, Dai, Yingbo, Tang, Yuxin, Yang, Jianfu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6308085/
https://www.ncbi.nlm.nih.gov/pubmed/30430771
http://dx.doi.org/10.1002/cam4.1871
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author Wei, Jingchao
Gan, Yu
Peng, Dongyi
Jiang, Xianzhen
Kitazawa, Riko
Xiang, Yali
Dai, Yingbo
Tang, Yuxin
Yang, Jianfu
author_facet Wei, Jingchao
Gan, Yu
Peng, Dongyi
Jiang, Xianzhen
Kitazawa, Riko
Xiang, Yali
Dai, Yingbo
Tang, Yuxin
Yang, Jianfu
author_sort Wei, Jingchao
collection PubMed
description The role of TDRG1 in tumorigenesis and the progression of seminoma, as well as its role in regulating chemosensitivity of seminoma to cisplatin through the PI3K/Akt/mTOR signaling pathway, has been previously defined. However, the detailed mechanism underlying TDRG1 expression and concomitant chemoresistance conditions are unknown. Furthermore, it has been reported that non‐protein‐coding RNAs play an important role in a variety of vital processes including cellular chemosensitivity. However, the role of non‐protein‐coding RNAs in regulating the chemosensitivity of seminoma remains unknown. In this study, using microarray analysis, we found that long non‐coding RNA H19 was upregulated while miRNA‐106b‐5p was downregulated in an established cisplatin‐resistant TCam‐2 cell line. Moreover, H19 acts as a miRNA‐106b‐5p sponge and thus impairs the function of miRNA‐106b‐5p on its target gene, TDRG1. Based on these findings, we propose that H19 promotes the expression of TDRG1 by sequestering miRNA‐106b‐5p and uses this mechanism to facilitate cell survival in cisplatin‐based chemotherapeutic conditions. These findings elucidate the mechanisms, at least partially, applied to deregulate TDRG1 and cisplatin sensitivity, and may provide new therapeutic possibilities for chemoresistant seminoma.
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spelling pubmed-63080852019-01-03 Long non‐coding RNA H19 promotes TDRG1 expression and cisplatin resistance by sequestering miRNA‐106b‐5p in seminoma Wei, Jingchao Gan, Yu Peng, Dongyi Jiang, Xianzhen Kitazawa, Riko Xiang, Yali Dai, Yingbo Tang, Yuxin Yang, Jianfu Cancer Med Cancer Biology The role of TDRG1 in tumorigenesis and the progression of seminoma, as well as its role in regulating chemosensitivity of seminoma to cisplatin through the PI3K/Akt/mTOR signaling pathway, has been previously defined. However, the detailed mechanism underlying TDRG1 expression and concomitant chemoresistance conditions are unknown. Furthermore, it has been reported that non‐protein‐coding RNAs play an important role in a variety of vital processes including cellular chemosensitivity. However, the role of non‐protein‐coding RNAs in regulating the chemosensitivity of seminoma remains unknown. In this study, using microarray analysis, we found that long non‐coding RNA H19 was upregulated while miRNA‐106b‐5p was downregulated in an established cisplatin‐resistant TCam‐2 cell line. Moreover, H19 acts as a miRNA‐106b‐5p sponge and thus impairs the function of miRNA‐106b‐5p on its target gene, TDRG1. Based on these findings, we propose that H19 promotes the expression of TDRG1 by sequestering miRNA‐106b‐5p and uses this mechanism to facilitate cell survival in cisplatin‐based chemotherapeutic conditions. These findings elucidate the mechanisms, at least partially, applied to deregulate TDRG1 and cisplatin sensitivity, and may provide new therapeutic possibilities for chemoresistant seminoma. John Wiley and Sons Inc. 2018-11-14 /pmc/articles/PMC6308085/ /pubmed/30430771 http://dx.doi.org/10.1002/cam4.1871 Text en © 2018 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cancer Biology
Wei, Jingchao
Gan, Yu
Peng, Dongyi
Jiang, Xianzhen
Kitazawa, Riko
Xiang, Yali
Dai, Yingbo
Tang, Yuxin
Yang, Jianfu
Long non‐coding RNA H19 promotes TDRG1 expression and cisplatin resistance by sequestering miRNA‐106b‐5p in seminoma
title Long non‐coding RNA H19 promotes TDRG1 expression and cisplatin resistance by sequestering miRNA‐106b‐5p in seminoma
title_full Long non‐coding RNA H19 promotes TDRG1 expression and cisplatin resistance by sequestering miRNA‐106b‐5p in seminoma
title_fullStr Long non‐coding RNA H19 promotes TDRG1 expression and cisplatin resistance by sequestering miRNA‐106b‐5p in seminoma
title_full_unstemmed Long non‐coding RNA H19 promotes TDRG1 expression and cisplatin resistance by sequestering miRNA‐106b‐5p in seminoma
title_short Long non‐coding RNA H19 promotes TDRG1 expression and cisplatin resistance by sequestering miRNA‐106b‐5p in seminoma
title_sort long non‐coding rna h19 promotes tdrg1 expression and cisplatin resistance by sequestering mirna‐106b‐5p in seminoma
topic Cancer Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6308085/
https://www.ncbi.nlm.nih.gov/pubmed/30430771
http://dx.doi.org/10.1002/cam4.1871
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