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Prospects of antibodies targeting CD47 or CD24 in the treatment of glioblastoma
Glioma is a malignant tumor with the highest incidence among all brain tumors (about 46% of intracranial tumors) and is the most common primary intracranial tumor. Among them, glioblastoma (GBM) is highly malignant and is one of the three refractory tumors with the highest mortality rate in the worl...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446212/ https://www.ncbi.nlm.nih.gov/pubmed/34363319 http://dx.doi.org/10.1111/cns.13714 |
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author | Wu, Hao Liu, Jialin Wang, Zhifei Yuan, Wen Chen, Ling |
author_facet | Wu, Hao Liu, Jialin Wang, Zhifei Yuan, Wen Chen, Ling |
author_sort | Wu, Hao |
collection | PubMed |
description | Glioma is a malignant tumor with the highest incidence among all brain tumors (about 46% of intracranial tumors) and is the most common primary intracranial tumor. Among them, glioblastoma (GBM) is highly malignant and is one of the three refractory tumors with the highest mortality rate in the world. The survival time from glioblastoma diagnosis to death is only 14–16 months for patients with standard treatment such as surgery plus radiotherapy and chemotherapy. Due to its high malignancy and poor prognosis, in‐depth studies have been conducted to explore effective therapeutic strategies for glioblastoma. In addition to the conventional surgery, radiotherapy, and chemotherapy, the glioblastoma treatments also include targeted therapy, immunotherapy, and electric field treatment. However, current treatment methods provide limited benefits because of the heterogeneity of glioblastoma and the complexity of the immune microenvironment within a tumor. Therefore, seeking an effective treatment plan is imperative. In particular, developing an active immunotherapy for glioblastoma has become an essential objective in the field. This article reviews the feasibility of CD47/CD24 antibody treatment, either individually or in combination, to target the tumor stem cells and the antitumor immunity in glioblastoma. The potential mechanisms underlying the antitumor effects of CD47/CD24 antibodies are also discussed. |
format | Online Article Text |
id | pubmed-8446212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84462122021-09-22 Prospects of antibodies targeting CD47 or CD24 in the treatment of glioblastoma Wu, Hao Liu, Jialin Wang, Zhifei Yuan, Wen Chen, Ling CNS Neurosci Ther Review Article Glioma is a malignant tumor with the highest incidence among all brain tumors (about 46% of intracranial tumors) and is the most common primary intracranial tumor. Among them, glioblastoma (GBM) is highly malignant and is one of the three refractory tumors with the highest mortality rate in the world. The survival time from glioblastoma diagnosis to death is only 14–16 months for patients with standard treatment such as surgery plus radiotherapy and chemotherapy. Due to its high malignancy and poor prognosis, in‐depth studies have been conducted to explore effective therapeutic strategies for glioblastoma. In addition to the conventional surgery, radiotherapy, and chemotherapy, the glioblastoma treatments also include targeted therapy, immunotherapy, and electric field treatment. However, current treatment methods provide limited benefits because of the heterogeneity of glioblastoma and the complexity of the immune microenvironment within a tumor. Therefore, seeking an effective treatment plan is imperative. In particular, developing an active immunotherapy for glioblastoma has become an essential objective in the field. This article reviews the feasibility of CD47/CD24 antibody treatment, either individually or in combination, to target the tumor stem cells and the antitumor immunity in glioblastoma. The potential mechanisms underlying the antitumor effects of CD47/CD24 antibodies are also discussed. John Wiley and Sons Inc. 2021-08-06 /pmc/articles/PMC8446212/ /pubmed/34363319 http://dx.doi.org/10.1111/cns.13714 Text en © 2021 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Wu, Hao Liu, Jialin Wang, Zhifei Yuan, Wen Chen, Ling Prospects of antibodies targeting CD47 or CD24 in the treatment of glioblastoma |
title | Prospects of antibodies targeting CD47 or CD24 in the treatment of glioblastoma |
title_full | Prospects of antibodies targeting CD47 or CD24 in the treatment of glioblastoma |
title_fullStr | Prospects of antibodies targeting CD47 or CD24 in the treatment of glioblastoma |
title_full_unstemmed | Prospects of antibodies targeting CD47 or CD24 in the treatment of glioblastoma |
title_short | Prospects of antibodies targeting CD47 or CD24 in the treatment of glioblastoma |
title_sort | prospects of antibodies targeting cd47 or cd24 in the treatment of glioblastoma |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446212/ https://www.ncbi.nlm.nih.gov/pubmed/34363319 http://dx.doi.org/10.1111/cns.13714 |
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