Role of TRAP1 Protein in the Development and Progression of Glioblastoma

Glioblastoma is recognized as the most aggressive type of primary brain tumor. Despite recent advances in understanding the molecular mechanisms involved in the biology of glioblastoma, patient survival rates remain disappointing, primarily due to the lack of effective treatment options. Tumor necro...

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Main Authors: I. F. Gareev, A. S. Yasinskaya, S. A. Roumiantsev, A. A. Bukhvostov
Format: Article
Language:English
Published: Bashkir State Medical University 2024-12-01
Series:Креативная хирургия и онкология
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Online Access:https://www.surgonco.ru/jour/article/view/1023
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author I. F. Gareev
A. S. Yasinskaya
S. A. Roumiantsev
A. A. Bukhvostov
author_facet I. F. Gareev
A. S. Yasinskaya
S. A. Roumiantsev
A. A. Bukhvostov
author_sort I. F. Gareev
collection DOAJ
description Glioblastoma is recognized as the most aggressive type of primary brain tumor. Despite recent advances in understanding the molecular mechanisms involved in the biology of glioblastoma, patient survival rates remain disappointing, primarily due to the lack of effective treatment options. Tumor necrosis factor receptor-associated protein 1 (TRAP1), a member of the heat shock protein 90 (Hsp90) family, refers to a protein predominantly localized in the mitochondria that regulates both cellular metabolic reprogramming and mitochondrial apoptosis. This protein is highly expressed in several types of tumors, including colorectal cancer, breast cancer, prostate cancer, and lung cancer, and is often associated with drug resistance. However, TRAP1 is also downregulated in certain cancers such as ovarian cancer, bladder cancer, and renal cancer, where its lower expression correlates with poorer prognoses and chemoresistance. The role of TRAP1 lies in enhancing or suppressing oxidative phosphorylation, with the impact of such regulation on tumor development and progression being a matter of ongoing debate. These observations prompt further investigation into the mechanisms responsible for the dual role of TRAP1 as both an oncogene and a tumor suppressor in specific types of tumors, particularly glioblastoma. The present study reviews the role of TRAP1 in the development and progression of glioblastoma and discusses the potential of targeting TRAP1 as a novel therapeutic approach against tumors.
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issn 2076-3093
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publishDate 2024-12-01
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series Креативная хирургия и онкология
spelling doaj-art-d22feecf994e4e74a379d9955ee681a82025-08-20T03:39:58ZengBashkir State Medical UniversityКреативная хирургия и онкология2076-30932307-05012024-12-0114436938110.24060/2076-3093-2024-14-4-369-381603Role of TRAP1 Protein in the Development and Progression of GlioblastomaI. F. Gareev0A. S. Yasinskaya1S. A. Roumiantsev2A. A. Bukhvostov3Central Research Laboratory, Bashkir State Medical University; Pirogov Russian National Research Medical UniversityClinical Emergency HospitalPirogov Russian National Research Medical University; National Medical Endocrinology Research CentrePirogov Russian National Research Medical UniversityGlioblastoma is recognized as the most aggressive type of primary brain tumor. Despite recent advances in understanding the molecular mechanisms involved in the biology of glioblastoma, patient survival rates remain disappointing, primarily due to the lack of effective treatment options. Tumor necrosis factor receptor-associated protein 1 (TRAP1), a member of the heat shock protein 90 (Hsp90) family, refers to a protein predominantly localized in the mitochondria that regulates both cellular metabolic reprogramming and mitochondrial apoptosis. This protein is highly expressed in several types of tumors, including colorectal cancer, breast cancer, prostate cancer, and lung cancer, and is often associated with drug resistance. However, TRAP1 is also downregulated in certain cancers such as ovarian cancer, bladder cancer, and renal cancer, where its lower expression correlates with poorer prognoses and chemoresistance. The role of TRAP1 lies in enhancing or suppressing oxidative phosphorylation, with the impact of such regulation on tumor development and progression being a matter of ongoing debate. These observations prompt further investigation into the mechanisms responsible for the dual role of TRAP1 as both an oncogene and a tumor suppressor in specific types of tumors, particularly glioblastoma. The present study reviews the role of TRAP1 in the development and progression of glioblastoma and discusses the potential of targeting TRAP1 as a novel therapeutic approach against tumors.https://www.surgonco.ru/jour/article/view/1023glioblastomatrap1oncogenesistargeted therapymetabolismstem cellsapoptosis
spellingShingle I. F. Gareev
A. S. Yasinskaya
S. A. Roumiantsev
A. A. Bukhvostov
Role of TRAP1 Protein in the Development and Progression of Glioblastoma
Креативная хирургия и онкология
glioblastoma
trap1
oncogenesis
targeted therapy
metabolism
stem cells
apoptosis
title Role of TRAP1 Protein in the Development and Progression of Glioblastoma
title_full Role of TRAP1 Protein in the Development and Progression of Glioblastoma
title_fullStr Role of TRAP1 Protein in the Development and Progression of Glioblastoma
title_full_unstemmed Role of TRAP1 Protein in the Development and Progression of Glioblastoma
title_short Role of TRAP1 Protein in the Development and Progression of Glioblastoma
title_sort role of trap1 protein in the development and progression of glioblastoma
topic glioblastoma
trap1
oncogenesis
targeted therapy
metabolism
stem cells
apoptosis
url https://www.surgonco.ru/jour/article/view/1023
work_keys_str_mv AT ifgareev roleoftrap1proteininthedevelopmentandprogressionofglioblastoma
AT asyasinskaya roleoftrap1proteininthedevelopmentandprogressionofglioblastoma
AT saroumiantsev roleoftrap1proteininthedevelopmentandprogressionofglioblastoma
AT aabukhvostov roleoftrap1proteininthedevelopmentandprogressionofglioblastoma