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The effects of statin therapy on brain tumors, particularly glioma: a review

Brain tumors account for less than 2% of all malignancies. However, they are associated with the highest morbidity and mortality rates among all solid tumors. The most common malignant primary brain tumors are glioma or glioblastoma (GBM), which have a median survival time of about 14 months, often...

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Autores principales: Alrosan, Amjad Z., Heilat, Ghaith B., Al Subeh, Zeinab Y., Alrosan, Khaled, Alrousan, Alaa F., Abu-Safieh, Amro K., Alabdallat, Nuwar S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10501357/
https://www.ncbi.nlm.nih.gov/pubmed/37466094
http://dx.doi.org/10.1097/CAD.0000000000001533
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author Alrosan, Amjad Z.
Heilat, Ghaith B.
Al Subeh, Zeinab Y.
Alrosan, Khaled
Alrousan, Alaa F.
Abu-Safieh, Amro K.
Alabdallat, Nuwar S.
author_facet Alrosan, Amjad Z.
Heilat, Ghaith B.
Al Subeh, Zeinab Y.
Alrosan, Khaled
Alrousan, Alaa F.
Abu-Safieh, Amro K.
Alabdallat, Nuwar S.
author_sort Alrosan, Amjad Z.
collection PubMed
description Brain tumors account for less than 2% of all malignancies. However, they are associated with the highest morbidity and mortality rates among all solid tumors. The most common malignant primary brain tumors are glioma or glioblastoma (GBM), which have a median survival time of about 14 months, often suffer from recurrence after a few months following treatment, and pose a therapeutic challenge. Despite recent therapeutic advances, the prognosis for glioma patients is poor when treated with modern therapies, including chemotherapy, surgery, radiation, or a combination of these. Therefore, discovering a new target to treat brain tumors, particularly glioma, might be advantageous in raising progression-free survival and overall survival (OS) rates. Statins, also known as competitive HMG-CoA reductase inhibitors, are effective medications for reducing cholesterol and cardiovascular risk. The use of statins prior to and during other cancer treatments appears to enhance patient outcomes according to preclinical studies. After surgical resection followed by concurrent radiation and treatment, OS for patients with GBM is only about a year. Statins have recently emerged as potential adjuvant medications for treating GBM due to their ability to inhibit cell growth, survival, migration, metastasis, inflammation, angiogenesis, and increase apoptosis in-vitro and in-vivo studies. Whether statins enhance clinical outcomes, such as patient survival in GBM, is still debatable. This study aimed to explore the effects of statin therapy in the context of cancer treatment, with a particular focus on GBM.
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spelling pubmed-105013572023-09-15 The effects of statin therapy on brain tumors, particularly glioma: a review Alrosan, Amjad Z. Heilat, Ghaith B. Al Subeh, Zeinab Y. Alrosan, Khaled Alrousan, Alaa F. Abu-Safieh, Amro K. Alabdallat, Nuwar S. Anticancer Drugs Review Articles Brain tumors account for less than 2% of all malignancies. However, they are associated with the highest morbidity and mortality rates among all solid tumors. The most common malignant primary brain tumors are glioma or glioblastoma (GBM), which have a median survival time of about 14 months, often suffer from recurrence after a few months following treatment, and pose a therapeutic challenge. Despite recent therapeutic advances, the prognosis for glioma patients is poor when treated with modern therapies, including chemotherapy, surgery, radiation, or a combination of these. Therefore, discovering a new target to treat brain tumors, particularly glioma, might be advantageous in raising progression-free survival and overall survival (OS) rates. Statins, also known as competitive HMG-CoA reductase inhibitors, are effective medications for reducing cholesterol and cardiovascular risk. The use of statins prior to and during other cancer treatments appears to enhance patient outcomes according to preclinical studies. After surgical resection followed by concurrent radiation and treatment, OS for patients with GBM is only about a year. Statins have recently emerged as potential adjuvant medications for treating GBM due to their ability to inhibit cell growth, survival, migration, metastasis, inflammation, angiogenesis, and increase apoptosis in-vitro and in-vivo studies. Whether statins enhance clinical outcomes, such as patient survival in GBM, is still debatable. This study aimed to explore the effects of statin therapy in the context of cancer treatment, with a particular focus on GBM. Lippincott Williams & Wilkins 2023-10 2023-07-19 /pmc/articles/PMC10501357/ /pubmed/37466094 http://dx.doi.org/10.1097/CAD.0000000000001533 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Review Articles
Alrosan, Amjad Z.
Heilat, Ghaith B.
Al Subeh, Zeinab Y.
Alrosan, Khaled
Alrousan, Alaa F.
Abu-Safieh, Amro K.
Alabdallat, Nuwar S.
The effects of statin therapy on brain tumors, particularly glioma: a review
title The effects of statin therapy on brain tumors, particularly glioma: a review
title_full The effects of statin therapy on brain tumors, particularly glioma: a review
title_fullStr The effects of statin therapy on brain tumors, particularly glioma: a review
title_full_unstemmed The effects of statin therapy on brain tumors, particularly glioma: a review
title_short The effects of statin therapy on brain tumors, particularly glioma: a review
title_sort effects of statin therapy on brain tumors, particularly glioma: a review
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10501357/
https://www.ncbi.nlm.nih.gov/pubmed/37466094
http://dx.doi.org/10.1097/CAD.0000000000001533
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