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circ_PTN contributes to -cisplatin resistance in glioblastoma via PI3K/AKT signaling through the miR-542-3p/PIK3R3 pathway
Glioblastoma has been identified as the most common and aggressive primary brain tumor in adults. Recently, it has been found that cisplatin (DDP) treatment is a common chemotherapeutic method for GBM patients. circ_PTN (ID number: hsa_circ_0003949) is a newly found circular (circRNA) which has been...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607136/ https://www.ncbi.nlm.nih.gov/pubmed/34853725 http://dx.doi.org/10.1016/j.omtn.2021.08.034 |
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author | Luo, Hongcheng Yi, Tingzhuang Huang, Deyou Chen, Xiaoping Li, Xu Wan, Qianquan Huang, Haineng Huang, Huadong Wei, Hongyu Song, Ye Que, Tianshi Hu, Rentong Huang, Huatuo Luo, Kunxiang Li, Chuanyu Qin, Chengjian Zheng, Chuanhua Lan, Chuanliu Chen, Wencheng Zhou, Dan Luo, Qisheng |
author_facet | Luo, Hongcheng Yi, Tingzhuang Huang, Deyou Chen, Xiaoping Li, Xu Wan, Qianquan Huang, Haineng Huang, Huadong Wei, Hongyu Song, Ye Que, Tianshi Hu, Rentong Huang, Huatuo Luo, Kunxiang Li, Chuanyu Qin, Chengjian Zheng, Chuanhua Lan, Chuanliu Chen, Wencheng Zhou, Dan Luo, Qisheng |
author_sort | Luo, Hongcheng |
collection | PubMed |
description | Glioblastoma has been identified as the most common and aggressive primary brain tumor in adults. Recently, it has been found that cisplatin (DDP) treatment is a common chemotherapeutic method for GBM patients. circ_PTN (ID number: hsa_circ_0003949) is a newly found circular (circRNA) which has been proved to be highly expressed in GBM cells, while its role in GBM remains unclear. Therefore, our study focused on investigating the role of circ_PTN in the DDP resistance of GBM cells. The expression of circ_PTN in DDP-sensitive and DDP-resistant GBM cells was detected in our assay. Functional experiments were utilized to unveil the effects of circ_PTN on the DDP resistance of GBM cells. Moreover, mechanism assays were conducted to confirm the mechanism of how circ_PTN affected the DDP resistance of GBM cells. According to the results, we found that circ_PTN promoted the DDP resistance of GBM cells through activation of the PI3K/AKT pathway. Moreover, circ_PTN silencing inhibited the DDP resistance of GBM tumors in vivo. To conclude, our study unveiled the influence of circ_PTN on the DDP resistance of GBM cells, which might provide a therapeutic target for GBM treatment via DDP. |
format | Online Article Text |
id | pubmed-8607136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-86071362021-11-30 circ_PTN contributes to -cisplatin resistance in glioblastoma via PI3K/AKT signaling through the miR-542-3p/PIK3R3 pathway Luo, Hongcheng Yi, Tingzhuang Huang, Deyou Chen, Xiaoping Li, Xu Wan, Qianquan Huang, Haineng Huang, Huadong Wei, Hongyu Song, Ye Que, Tianshi Hu, Rentong Huang, Huatuo Luo, Kunxiang Li, Chuanyu Qin, Chengjian Zheng, Chuanhua Lan, Chuanliu Chen, Wencheng Zhou, Dan Luo, Qisheng Mol Ther Nucleic Acids Original Article Glioblastoma has been identified as the most common and aggressive primary brain tumor in adults. Recently, it has been found that cisplatin (DDP) treatment is a common chemotherapeutic method for GBM patients. circ_PTN (ID number: hsa_circ_0003949) is a newly found circular (circRNA) which has been proved to be highly expressed in GBM cells, while its role in GBM remains unclear. Therefore, our study focused on investigating the role of circ_PTN in the DDP resistance of GBM cells. The expression of circ_PTN in DDP-sensitive and DDP-resistant GBM cells was detected in our assay. Functional experiments were utilized to unveil the effects of circ_PTN on the DDP resistance of GBM cells. Moreover, mechanism assays were conducted to confirm the mechanism of how circ_PTN affected the DDP resistance of GBM cells. According to the results, we found that circ_PTN promoted the DDP resistance of GBM cells through activation of the PI3K/AKT pathway. Moreover, circ_PTN silencing inhibited the DDP resistance of GBM tumors in vivo. To conclude, our study unveiled the influence of circ_PTN on the DDP resistance of GBM cells, which might provide a therapeutic target for GBM treatment via DDP. American Society of Gene & Cell Therapy 2021-09-07 /pmc/articles/PMC8607136/ /pubmed/34853725 http://dx.doi.org/10.1016/j.omtn.2021.08.034 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Original Article Luo, Hongcheng Yi, Tingzhuang Huang, Deyou Chen, Xiaoping Li, Xu Wan, Qianquan Huang, Haineng Huang, Huadong Wei, Hongyu Song, Ye Que, Tianshi Hu, Rentong Huang, Huatuo Luo, Kunxiang Li, Chuanyu Qin, Chengjian Zheng, Chuanhua Lan, Chuanliu Chen, Wencheng Zhou, Dan Luo, Qisheng circ_PTN contributes to -cisplatin resistance in glioblastoma via PI3K/AKT signaling through the miR-542-3p/PIK3R3 pathway |
title | circ_PTN contributes to -cisplatin resistance in glioblastoma via PI3K/AKT signaling through the miR-542-3p/PIK3R3 pathway |
title_full | circ_PTN contributes to -cisplatin resistance in glioblastoma via PI3K/AKT signaling through the miR-542-3p/PIK3R3 pathway |
title_fullStr | circ_PTN contributes to -cisplatin resistance in glioblastoma via PI3K/AKT signaling through the miR-542-3p/PIK3R3 pathway |
title_full_unstemmed | circ_PTN contributes to -cisplatin resistance in glioblastoma via PI3K/AKT signaling through the miR-542-3p/PIK3R3 pathway |
title_short | circ_PTN contributes to -cisplatin resistance in glioblastoma via PI3K/AKT signaling through the miR-542-3p/PIK3R3 pathway |
title_sort | circ_ptn contributes to -cisplatin resistance in glioblastoma via pi3k/akt signaling through the mir-542-3p/pik3r3 pathway |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607136/ https://www.ncbi.nlm.nih.gov/pubmed/34853725 http://dx.doi.org/10.1016/j.omtn.2021.08.034 |
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