Deciphering immune microenvironment and cell evasion mechanisms in human gliomas
Gliomas are considered one of the most malignant cancers in the body. Despite current therapies, including surgery, chemotherapy, and radiotherapy, these tumors usually recur with more aggressive and resistant phenotypes. Indeed, the survival following these conventional therapies is very poor, whic...
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Published in | Frontiers in oncology Vol. 13; p. 1135430 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Frontiers Media S.A
19.05.2023
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Abstract | Gliomas are considered one of the most malignant cancers in the body. Despite current therapies, including surgery, chemotherapy, and radiotherapy, these tumors usually recur with more aggressive and resistant phenotypes. Indeed, the survival following these conventional therapies is very poor, which makes immunotherapy the subject of active research at present. The anti-tumor immune response could also be considered a prognostic factor since each stage of cancer development is regulated by immune cells. However, glioma microenvironment contains malignant cells that secrete numerous chemokines, cytokines and growth factors, promoting the infiltration of immunosuppressive cells into the tumor, which limit the functioning of the immune system against glioma cells. Recently, researchers have been able to reverse the immune resistance of cancer cells and thus activate the anti-tumor immune response through different immunotherapy strategies. Here, we review the general concept of glioma’s immune microenvironment and report the impact of its distinct components on the anti-tumor immune response. We also discuss the mechanisms of glioma cell evasion from the immune response and pinpoint some potential therapeutic pathways, which could alleviate such resistance. |
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AbstractList | Gliomas are considered one of the most malignant cancers in the body. Despite current therapies, including surgery, chemotherapy, and radiotherapy, these tumors usually recur with more aggressive and resistant phenotypes. Indeed, the survival following these conventional therapies is very poor, which makes immunotherapy the subject of active research at present. The anti-tumor immune response could also be considered a prognostic factor since each stage of cancer development is regulated by immune cells. However, glioma microenvironment contains malignant cells that secrete numerous chemokines, cytokines and growth factors, promoting the infiltration of immunosuppressive cells into the tumor, which limit the functioning of the immune system against glioma cells. Recently, researchers have been able to reverse the immune resistance of cancer cells and thus activate the anti-tumor immune response through different immunotherapy strategies. Here, we review the general concept of glioma’s immune microenvironment and report the impact of its distinct components on the anti-tumor immune response. We also discuss the mechanisms of glioma cell evasion from the immune response and pinpoint some potential therapeutic pathways, which could alleviate such resistance. Gliomas are considered one of the most malignant cancers in the body. Despite current therapies, including surgery, chemotherapy, and radiotherapy, these tumors usually recur with more aggressive and resistant phenotypes. Indeed, the survival following these conventional therapies is very poor, which makes immunotherapy the subject of active research at present. The anti-tumor immune response could also be considered a prognostic factor since each stage of cancer development is regulated by immune cells. However, glioma microenvironment contains malignant cells that secrete numerous chemokines, cytokines and growth factors, promoting the infiltration of immunosuppressive cells into the tumor, which limit the functioning of the immune system against glioma cells. Recently, researchers have been able to reverse the immune resistance of cancer cells and thus activate the anti-tumor immune response through different immunotherapy strategies. Here, we review the general concept of glioma's immune microenvironment and report the impact of its distinct components on the anti-tumor immune response. We also discuss the mechanisms of glioma cell evasion from the immune response and pinpoint some potential therapeutic pathways, which could alleviate such resistance.Gliomas are considered one of the most malignant cancers in the body. Despite current therapies, including surgery, chemotherapy, and radiotherapy, these tumors usually recur with more aggressive and resistant phenotypes. Indeed, the survival following these conventional therapies is very poor, which makes immunotherapy the subject of active research at present. The anti-tumor immune response could also be considered a prognostic factor since each stage of cancer development is regulated by immune cells. However, glioma microenvironment contains malignant cells that secrete numerous chemokines, cytokines and growth factors, promoting the infiltration of immunosuppressive cells into the tumor, which limit the functioning of the immune system against glioma cells. Recently, researchers have been able to reverse the immune resistance of cancer cells and thus activate the anti-tumor immune response through different immunotherapy strategies. Here, we review the general concept of glioma's immune microenvironment and report the impact of its distinct components on the anti-tumor immune response. We also discuss the mechanisms of glioma cell evasion from the immune response and pinpoint some potential therapeutic pathways, which could alleviate such resistance. |
Author | Badou, Abdallah Reddy, Konala Priyanka Rafii, Soumaya Kandoussi, Sarah Ghouzlani, Amina Naji, Oumayma Ullah Sadiqi, Rizwan |
AuthorAffiliation | 3 Faculty of Science and Technology, Middlesex University , London , United Kingdom 4 Mohammed VI Center for Research and Innovation, Rabat, Morocco and Mohammed VI University of Sciences and Health , Casablanca , Morocco 1 Immuno-Genetics and Human Pathologies Laboratory, Faculty of Medicine and Pharmacy, Hassan II University , Casablanca , Morocco 2 Faculty of Medicine, Medical University of Pleven , Pleven , Bulgaria |
AuthorAffiliation_xml | – name: 4 Mohammed VI Center for Research and Innovation, Rabat, Morocco and Mohammed VI University of Sciences and Health , Casablanca , Morocco – name: 1 Immuno-Genetics and Human Pathologies Laboratory, Faculty of Medicine and Pharmacy, Hassan II University , Casablanca , Morocco – name: 3 Faculty of Science and Technology, Middlesex University , London , United Kingdom – name: 2 Faculty of Medicine, Medical University of Pleven , Pleven , Bulgaria |
Author_xml | – sequence: 1 givenname: Soumaya surname: Rafii fullname: Rafii, Soumaya – sequence: 2 givenname: Sarah surname: Kandoussi fullname: Kandoussi, Sarah – sequence: 3 givenname: Amina surname: Ghouzlani fullname: Ghouzlani, Amina – sequence: 4 givenname: Oumayma surname: Naji fullname: Naji, Oumayma – sequence: 5 givenname: Konala Priyanka surname: Reddy fullname: Reddy, Konala Priyanka – sequence: 6 givenname: Rizwan surname: Ullah Sadiqi fullname: Ullah Sadiqi, Rizwan – sequence: 7 givenname: Abdallah surname: Badou fullname: Badou, Abdallah |
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Copyright | Copyright © 2023 Rafii, Kandoussi, Ghouzlani, Naji, Reddy, Ullah Sadiqi and Badou. Copyright © 2023 Rafii, Kandoussi, Ghouzlani, Naji, Reddy, Ullah Sadiqi and Badou 2023 Rafii, Kandoussi, Ghouzlani, Naji, Reddy, Ullah Sadiqi and Badou |
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Keywords | glioma immune microenvironment glioma cell evasion immunotherapy immune checkpoints therapy resistance |
Language | English |
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