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The Cellular Prion Protein: A Promising Therapeutic Target for Cancer

Studies on the cellular prion protein (PrP(C)) have been actively conducted because misfolded PrP(C) is known to cause transmissible spongiform encephalopathies or prion disease. PrP(C) is a glycophosphatidylinositol-anchored cell surface glycoprotein that has been reported to affect several cellula...

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Detalles Bibliográficos
Autores principales: Go, Gyeongyun, Lee, Sang Hun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730109/
https://www.ncbi.nlm.nih.gov/pubmed/33276687
http://dx.doi.org/10.3390/ijms21239208
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author Go, Gyeongyun
Lee, Sang Hun
author_facet Go, Gyeongyun
Lee, Sang Hun
author_sort Go, Gyeongyun
collection PubMed
description Studies on the cellular prion protein (PrP(C)) have been actively conducted because misfolded PrP(C) is known to cause transmissible spongiform encephalopathies or prion disease. PrP(C) is a glycophosphatidylinositol-anchored cell surface glycoprotein that has been reported to affect several cellular functions such as stress protection, cellular differentiation, mitochondrial homeostasis, circadian rhythm, myelin homeostasis, and immune modulation. Recently, it has also been reported that PrP(C) mediates tumor progression by enhancing the proliferation, metastasis, and drug resistance of cancer cells. In addition, PrP(C) regulates cancer stem cell properties by interacting with cancer stem cell marker proteins. In this review, we summarize how PrP(C) promotes tumor progression in terms of proliferation, metastasis, drug resistance, and cancer stem cell properties. In addition, we discuss strategies to treat tumors by modulating the function and expression of PrP(C) via the regulation of HSPA1L/HIF-1α expression and using an anti-prion antibody.
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spelling pubmed-77301092020-12-12 The Cellular Prion Protein: A Promising Therapeutic Target for Cancer Go, Gyeongyun Lee, Sang Hun Int J Mol Sci Review Studies on the cellular prion protein (PrP(C)) have been actively conducted because misfolded PrP(C) is known to cause transmissible spongiform encephalopathies or prion disease. PrP(C) is a glycophosphatidylinositol-anchored cell surface glycoprotein that has been reported to affect several cellular functions such as stress protection, cellular differentiation, mitochondrial homeostasis, circadian rhythm, myelin homeostasis, and immune modulation. Recently, it has also been reported that PrP(C) mediates tumor progression by enhancing the proliferation, metastasis, and drug resistance of cancer cells. In addition, PrP(C) regulates cancer stem cell properties by interacting with cancer stem cell marker proteins. In this review, we summarize how PrP(C) promotes tumor progression in terms of proliferation, metastasis, drug resistance, and cancer stem cell properties. In addition, we discuss strategies to treat tumors by modulating the function and expression of PrP(C) via the regulation of HSPA1L/HIF-1α expression and using an anti-prion antibody. MDPI 2020-12-02 /pmc/articles/PMC7730109/ /pubmed/33276687 http://dx.doi.org/10.3390/ijms21239208 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Go, Gyeongyun
Lee, Sang Hun
The Cellular Prion Protein: A Promising Therapeutic Target for Cancer
title The Cellular Prion Protein: A Promising Therapeutic Target for Cancer
title_full The Cellular Prion Protein: A Promising Therapeutic Target for Cancer
title_fullStr The Cellular Prion Protein: A Promising Therapeutic Target for Cancer
title_full_unstemmed The Cellular Prion Protein: A Promising Therapeutic Target for Cancer
title_short The Cellular Prion Protein: A Promising Therapeutic Target for Cancer
title_sort cellular prion protein: a promising therapeutic target for cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730109/
https://www.ncbi.nlm.nih.gov/pubmed/33276687
http://dx.doi.org/10.3390/ijms21239208
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