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

Roller, Corinna 1; Maddalo, Danilo 1
1 Institut für Toxikologie und Genetik (ITG), Karlsruher Institut für Technologie (KIT)

Abstract:

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.


Volltext §
DOI: 10.5445/IR/1000039935
Originalveröffentlichung
DOI: 10.3389/fphar.2013.00010
Scopus
Zitationen: 112
Web of Science
Zitationen: 102
Dimensions
Zitationen: 116
Cover der Publikation
Zugehörige Institution(en) am KIT Institut für Toxikologie und Genetik (ITG)
Publikationstyp Zeitschriftenaufsatz
Publikationsjahr 2013
Sprache Englisch
Identifikator ISSN: 1663-9812
urn:nbn:de:swb:90-399358
KITopen-ID: 1000039935
HGF-Programm 47.02.01 (POF II, LK 01) Synth. biomimetische Werkzeuge ITG
Erschienen in Frontiers in pharmacology
Verlag Frontiers Media SA
Band 4
Seiten Article 10
Bemerkung zur Veröffentlichung Gefördert durch den KIT-Publikationsfonds
Schlagwörter cell stress, chaperone, drug resistance, therapy, unfolded protein response
Nachgewiesen in Scopus
Web of Science
Dimensions
Globale Ziele für nachhaltige Entwicklung Ziel 3 – Gesundheit und Wohlergehen
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