Zusammenfassung
„Molecular targeting” gewinnt auch bei der Suche nach neuen Therapiekonzepten für
das Prostatakarzinom durch zunehmendes Wissen um die molekulare Pathogenese an Bedeutung
[29 ]
[35 ]. Ein solches Targeting scheint besonders mit Proteasomeninhibitoren möglich. Proteasomen
sind multikatalytische Proteinasen, die (unter anderem) an zentralen Stellen des Zellzyklus
Proteine, speziell auch die der Apoptoseinduktion, degradieren. Bislang konnte mit
In-vitro-Untersuchungen die Wirksamkeit der Proteasomeninhibitoren bei der Apoptoseinduktion
belegt werden, ebenso wie ihre zusätzliche Verstärkung zytotoxischer und antitumoraler
Effekte. In vivo konnte bei Tieren und Patienten mit hormonrefraktären Prostatakarzinomen
eine Reduktion des Tumorvolumens und des prostataspezifischen Antigens (PSA) beobachtet
werden. PS-341 (Bortezomib, Velcade®) ist dabei der erste Proteasomeninhibitor, der
klinisch bei Tumoren angewendet und in Studien untersucht wurde. Die vorliegende Übersichtsarbeit
möchte die Verbindung zwischen den intrazellulären Wirkungen der Proteasomeninhibitoren
und der Apoptoseinduktion sowie den aktuellen Stand klinischer Untersuchungen darstellen
und diskutieren. Auch eigene Ergebisse der Proteasomeninhibition bei individuellen
Prostatakarzinom-Zelllinien werden vorgestellt. Insgesamt muss man davon ausgehen,
dass Proteasomeninhibitoren einen neuen therapeutischen Zugang im „molekularen Targeting”
des Prostatakarzinoms eröffnen könnten.
Abstract
New perspectives in prostate cancer genesis and putative clinical management have
emerged in recent years [29 ]
[35 ]. Apoptosis plays a major role in this environment. Proteasome inhibitors block the
action of a multicatalytic proteinase complex involved in the degradation of intracellular
proteins, particularly with regard to cell cycle regulation and apoptosis. Numerous
in vitro studies have demonstrated the ability of these compounds to induce apoptosis
and enhance the activity of conventional tumoricidal agents in many cancer cell types,
including prostate cancer cells. They point out the use of these potent inhibitors
as a new potential molecular approach to the therapeutic management of prostate cancer.
Furthermore, the action of proteasome inhibitors has been tested in animal models
and in patients with hormone refractory prostate cancer, resulting in both PSA and
tumor volume decrease. PS-341 (bortezomib, VelcadeTM ) is the first proteasome inhibitor with clinical application in cancer therapy that
has been used in clinical trials to date. This report reviews the current status of
those papers that have tried to analyze the connection between the proteasome pathway
and apoptosis. We present our results of proteasome inhibition in individual prostate
cancer cell lines. Proteasomal inhibition may offer a new therapeutic access in “molecular
targeting” of prostate cancer.
Schlüsselwörter
Prostatakarzinom/medikamentöse Therapie - Apoptose/Therapie/Physiologie - Boronate/Pharmakologie
- Proteasomeninhibitoren/Pharmakologie - klinische Studie - Multienzymkomplexe/Antagonisten
und Inhibitoren
Key words
Prostate cancer/drug therapy - apoptosis/drug effects/physiology - boronic acids/pharmacology
- protease inhibitors/pharmacology - clinical study on humans - multienzyme complexes/antagonists
and inhibitors
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Prof. Dr. Thomas Zwergel
Klinik für Urologie und Kinderurologie · Universitätskliniken des Saarlandes
66421 Homburg-Saar
Phone: 06841-16-24758
Fax: 06841-1624795
Email: thomas.zwergel@uniklinik-saarland.de