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A potentially effective drug for patients with recurrent glioma: sermorelin
BACKGROUND: Treatment insensitivity is the main cause of glioma. This study was designed to screen out effective drugs for recurrent gliomas based on the transcriptomics data. METHODS: A total of 1,018 glioma patients with transcriptome sequencing data and clinical data were included in this study....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033379/ https://www.ncbi.nlm.nih.gov/pubmed/33842627 http://dx.doi.org/10.21037/atm-20-6561 |
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author | Chang, Yuanhao Huang, Ruoyu Zhai, You Huang, Lijie Feng, Yuemei Wang, Di Chai, Ruichao Zhang, Wei Hu, Huimin |
author_facet | Chang, Yuanhao Huang, Ruoyu Zhai, You Huang, Lijie Feng, Yuemei Wang, Di Chai, Ruichao Zhang, Wei Hu, Huimin |
author_sort | Chang, Yuanhao |
collection | PubMed |
description | BACKGROUND: Treatment insensitivity is the main cause of glioma. This study was designed to screen out effective drugs for recurrent gliomas based on the transcriptomics data. METHODS: A total of 1,018 glioma patients with transcriptome sequencing data and clinical data were included in this study. There were 325 patients in the discovery cohort, including 229 primary patients and 92 recurrent patients. There were 693 patients in the validation cohort, including 422 primary patients and 271 relapsed patients. Drug Resistant Scores (DRS) of 4,865 drugs of each patient were used for screening. The analysis and drawing in this study were mainly based on R language. RESULTS: After high-throughput drug screening, we found that recurrent glioma patients were most sensitive to sermorelin. Further analysis revealed that sermorelin was suitable for recurrent patients with high grade, IDH-wildtype and 1p/19q non-codeletion status. GO and KEGG analyses found that sermorelin may inhibit tumor cell proliferation by cell cycle blocking. Moreover, sermorelin was also related to the immune system process and negatively regulated immune checkpoints and M0 macrophages. Lastly, the Kaplan–Meier method showed the patient's benefit from sermorelin was independent of postoperative adjuvant treatment. CONCLUSIONS: Recurrent glioma patients are sensitive to sermorelin and it makes effect through glioma cells proliferation inhibiting and immune response enhancing. |
format | Online Article Text |
id | pubmed-8033379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-80333792021-04-09 A potentially effective drug for patients with recurrent glioma: sermorelin Chang, Yuanhao Huang, Ruoyu Zhai, You Huang, Lijie Feng, Yuemei Wang, Di Chai, Ruichao Zhang, Wei Hu, Huimin Ann Transl Med Original Article BACKGROUND: Treatment insensitivity is the main cause of glioma. This study was designed to screen out effective drugs for recurrent gliomas based on the transcriptomics data. METHODS: A total of 1,018 glioma patients with transcriptome sequencing data and clinical data were included in this study. There were 325 patients in the discovery cohort, including 229 primary patients and 92 recurrent patients. There were 693 patients in the validation cohort, including 422 primary patients and 271 relapsed patients. Drug Resistant Scores (DRS) of 4,865 drugs of each patient were used for screening. The analysis and drawing in this study were mainly based on R language. RESULTS: After high-throughput drug screening, we found that recurrent glioma patients were most sensitive to sermorelin. Further analysis revealed that sermorelin was suitable for recurrent patients with high grade, IDH-wildtype and 1p/19q non-codeletion status. GO and KEGG analyses found that sermorelin may inhibit tumor cell proliferation by cell cycle blocking. Moreover, sermorelin was also related to the immune system process and negatively regulated immune checkpoints and M0 macrophages. Lastly, the Kaplan–Meier method showed the patient's benefit from sermorelin was independent of postoperative adjuvant treatment. CONCLUSIONS: Recurrent glioma patients are sensitive to sermorelin and it makes effect through glioma cells proliferation inhibiting and immune response enhancing. AME Publishing Company 2021-03 /pmc/articles/PMC8033379/ /pubmed/33842627 http://dx.doi.org/10.21037/atm-20-6561 Text en 2021 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Chang, Yuanhao Huang, Ruoyu Zhai, You Huang, Lijie Feng, Yuemei Wang, Di Chai, Ruichao Zhang, Wei Hu, Huimin A potentially effective drug for patients with recurrent glioma: sermorelin |
title | A potentially effective drug for patients with recurrent glioma: sermorelin |
title_full | A potentially effective drug for patients with recurrent glioma: sermorelin |
title_fullStr | A potentially effective drug for patients with recurrent glioma: sermorelin |
title_full_unstemmed | A potentially effective drug for patients with recurrent glioma: sermorelin |
title_short | A potentially effective drug for patients with recurrent glioma: sermorelin |
title_sort | potentially effective drug for patients with recurrent glioma: sermorelin |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033379/ https://www.ncbi.nlm.nih.gov/pubmed/33842627 http://dx.doi.org/10.21037/atm-20-6561 |
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