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The Molecular Chaperone GRP78/BiP in the Development of Chemoresistance: Mechanism and Possible Treatment

Treatment of several types of cancer such as lung, breast, prostate, and pancreas has shown notable progresses in the past decades. However, after an initial response, tumors eventually became resistant to chemotherapy. This phenomenon, known as chemoresistance, accounts for the death of most cancer...

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Detalles Bibliográficos
Autores principales: Roller, Corinna, Maddalo, Danilo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568707/
https://www.ncbi.nlm.nih.gov/pubmed/23403503
http://dx.doi.org/10.3389/fphar.2013.00010
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author Roller, Corinna
Maddalo, Danilo
author_facet Roller, Corinna
Maddalo, Danilo
author_sort Roller, Corinna
collection PubMed
description Treatment of several types of cancer such as lung, breast, prostate, and pancreas has shown notable progresses in the past decades. However, after an initial response, tumors eventually became resistant to chemotherapy. This phenomenon, known as chemoresistance, accounts for the death of most cancer patients. Several studies in patients refractory to therapy have revealed the upregulation of the molecular chaperone GRP78/Binding Protein, BiP (BiP) both at the RNA and protein expression level. Furthermore GRP78/BiP relocates to the cell membrane in malignant but not in benign cells. In this communication we review studies on the role and the mechanism of action of GRP78/BiP during development of chemoresistance in cancer cells. In addition we discuss the possible role of GRP78 as a biomarker and as a target in cancer therapy.
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spelling pubmed-35687072013-02-12 The Molecular Chaperone GRP78/BiP in the Development of Chemoresistance: Mechanism and Possible Treatment Roller, Corinna Maddalo, Danilo Front Pharmacol Pharmacology Treatment of several types of cancer such as lung, breast, prostate, and pancreas has shown notable progresses in the past decades. However, after an initial response, tumors eventually became resistant to chemotherapy. This phenomenon, known as chemoresistance, accounts for the death of most cancer patients. Several studies in patients refractory to therapy have revealed the upregulation of the molecular chaperone GRP78/Binding Protein, BiP (BiP) both at the RNA and protein expression level. Furthermore GRP78/BiP relocates to the cell membrane in malignant but not in benign cells. In this communication we review studies on the role and the mechanism of action of GRP78/BiP during development of chemoresistance in cancer cells. In addition we discuss the possible role of GRP78 as a biomarker and as a target in cancer therapy. Frontiers Media S.A. 2013-02-11 /pmc/articles/PMC3568707/ /pubmed/23403503 http://dx.doi.org/10.3389/fphar.2013.00010 Text en Copyright © 2013 Roller and Maddalo. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Pharmacology
Roller, Corinna
Maddalo, Danilo
The Molecular Chaperone GRP78/BiP in the Development of Chemoresistance: Mechanism and Possible Treatment
title The Molecular Chaperone GRP78/BiP in the Development of Chemoresistance: Mechanism and Possible Treatment
title_full The Molecular Chaperone GRP78/BiP in the Development of Chemoresistance: Mechanism and Possible Treatment
title_fullStr The Molecular Chaperone GRP78/BiP in the Development of Chemoresistance: Mechanism and Possible Treatment
title_full_unstemmed The Molecular Chaperone GRP78/BiP in the Development of Chemoresistance: Mechanism and Possible Treatment
title_short The Molecular Chaperone GRP78/BiP in the Development of Chemoresistance: Mechanism and Possible Treatment
title_sort molecular chaperone grp78/bip in the development of chemoresistance: mechanism and possible treatment
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568707/
https://www.ncbi.nlm.nih.gov/pubmed/23403503
http://dx.doi.org/10.3389/fphar.2013.00010
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