Zusammenfassung
Resistenz von Krebszellen gegen zytotoxische Chemotherapie ist eine wichtige Ursache für die oft unbefriedigenden Behandlungsergebnisse bei fortgeschrittenen Krebserkrankungen. Dabei sind Krebserkrankungen häufig nicht nur resistent gegen jene Substanzen, welche bereits verwendet wurden, sondern auch gegen eine Reihe anderer strukturell und funktionell unterschiedlicher Zytostatika. Ein ähnliches Verhalten zeigen Krebszellen bei einer bestimmten Form von experimenteller Chemotherapieresistenz, welche „multidrug resistance“ oder MDR genannt wird. Aufgrund dieser Ähnlichkeit mit klinischer Chemotherapieresistenz hat MDR großes Interesse ausgelöst. Wir wissen heute, daß MDR durch verschiedene molekulare Mechanismen verursacht werden kann. Dazu gehören erhöhte Expression von Transportproteinen wie P-Glykoprotein (Pgp) oder MRP („Multidrug-Resistance-Protein”), erhöhte Aktivität des Glutathion-Redox-Zyklus, oder verminderte Aktivität von Topoisomerase II α (1, 2). Derzeit am ausführlichsten erforscht ist die Pgp-bedingte MDR (Pgp-MDR). Dieser Beitrag ist ein Versuch, den derzeitigen Wissenstand über Pgp-MDR zusammenzufassen, mit Schwerpunkt auf Überwindung von Pgp-MDR durch Calciumantagonisten.
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© 1996 Dr. Dietrich Steinkopff Verlag, GmbH & Co. KG, Darmstadt
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Lehnert, M. (1996). Calciumantagonisten zur Überwindung von P-Glykoprotein-bedingter „Multidrug Resistance“ von Krebserkrankungen. In: Kübler, W., Tritthart, H.A. (eds) Calciumantagonisten. Steinkopff. https://doi.org/10.1007/978-3-642-93678-4_17
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DOI: https://doi.org/10.1007/978-3-642-93678-4_17
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