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An analog of withaferin a activates the MAPK and glutathione "stress" pathways and inhibits pancreatic cancer cell proliferation

  • Xiaobing Liu
  • , Wenqing Qi
  • , Laurence S. Cooke
  • , E. M. Kithsiri Wijeratne
  • , Ya Ming Xu
  • , Marilyn T. Marron
  • , A. A. Leslie Gunatilaka
  • , Daruka Mahadevan

Producción científica: Articlerevisión exhaustiva

Resumen

Withaferin A (WA) (1) and two analogs [4-epi-withaferin A (2) and 4,27-diacetyl-4-epi-withaferin A (3)] were evaluated for antitumor activity in pancreatic cancer cells. IC50 for 1, 2, and 3 were 0.87, 0.45, and 0.29 μM (BxPC-3); 1.28, 1.53, and 0.52 μM (MIAPaCa-2); and 0.59, 2.25, and 0.56 μM (PANC-1), respectively. We chose WA analog 3 for functional studies with confirmatory RT-PCR and Western blotting. ANOVA identified 33 (MIAPaCa-2), 54 (PANC-1), and 48 (BxPC-3) gene expression changes. Fisher exact test demonstrated MAPK and glutathione pathways to be overexpressed with WA analog 3. WA analog 3 elicits a dose-and time-dependent apoptosis, activates MAPK and glutathione "stress" pathways, and inhibits proliferation.

Idioma originalEnglish (US)
Páginas (desde-hasta)668-675
Número de páginas8
PublicaciónCancer Investigation
Volumen29
N.º10
DOI
EstadoPublished - nov 15 2011
Publicado de forma externa

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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