Chemosensitization of bladder cancer cells by survivin-directed antisense oligodeoxynucleotides and siRNA

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Susanne Fuessel - , Klinik und Poliklinik für Urologie (Autor:in)
  • Jana Herrmann - , Klinik und Poliklinik für Urologie (Autor:in)
  • Shuangli Ning - , Klinik und Poliklinik für Urologie (Autor:in)
  • Matthias Kotzsch - , Institut für Pathologie (Autor:in)
  • Kai Kraemer - , Klinik und Poliklinik für Urologie (Autor:in)
  • Uta Schmidt - , Klinik und Poliklinik für Urologie (Autor:in)
  • Oliver W. Hakenberg - , Klinik und Poliklinik für Urologie (Autor:in)
  • Manfred P. Wirth - , Klinik und Poliklinik für Urologie (Autor:in)
  • Axel Meye - , Klinik und Poliklinik für Urologie (Autor:in)

Abstract

Survivin is known to be overexpressed in numerous tumor types including human bladder cancer and to cause resistance to radiation and chemotherapy. Therefore, we tested the antisense oligodeoxynucleotide AS-SVV286 and the small interfering RNA si-SVV284 to down-regulate survivin in the BCa cell lines EJ28 and 5637 thereby acting as sensitizers for chemotherapy. Pretreatment with these inhibitors followed by chemotherapy caused an enhanced decrease in cell viability. The observed reduction in cell counts associated with increased rates of apoptosis paralleled the degree of reduction of survivin expression that was achieved more efficiently by the siRNA than by the AS-ODN. Nevertheless, both therapy approaches in combination with all tested chemotherapeutics provoked a remarkable inhibition of viability and may serve as suitable additive tools for chemosensitization of bladder cancer cells.

Details

OriginalspracheEnglisch
Seiten (von - bis)243-254
Seitenumfang12
FachzeitschriftCancer letters
Jahrgang232
Ausgabenummer2
PublikationsstatusVeröffentlicht - 8 Feb. 2006
Peer-Review-StatusJa

Externe IDs

PubMed 16458121

Schlagworte

Ziele für nachhaltige Entwicklung

ASJC Scopus Sachgebiete

Schlagwörter

  • Antisense oligodeoxnucleotides, Bladder cancer, Chemosensitization, siRNA, Survivin