Emodin potentiates the antitumor effects of gemcitabine in PANC-1 pancreatic cancer xenograft model in vivo via inhibition of inhibitors of apoptosis

  • Authors: Hong-Chun Guo, He-Qi Bu, Jiang Luo, Wei-Tian Wei, Dian-Lei Liu, Hui Chen, Hong-Fei Tong, Zhao-Hong Wang, Hua-Yong Wu, Hong-Hai Li, Ming-Ming Zuo, Wei Li, Sheng-Zhang Lin
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  • Published online on: Wednesday, February 29, 2012
  • Pages: 1849-1857
  • DOI: 10.3892/ijo.2012.1389

Abstract

Pancreatic cancer is a highly aggressive malignant disease. Gemcitabine is currently the standard first-line chemotherapeutic agent for pancreatic cancer. As members of apoptosis inhibitors, Survivin and XIAP play an important role in chemotherapy resistance in pancreatic cancer. Emodin has therapeutic potential against cancers. This study was designed to investigate whether combination therapy with gemcitabine and emodin enhanced antitumor efficacy in pancreatic cancer. The application of the combination therapy triggered significantly higher frequency of pancreatic cancer cell apoptosis. Our research demonstrated that the combination of emodin and gemcitabine resulted in significantly reduced tumor volumes compared to gemcitabine or emodin treatment alone. Immunohistochemistry and western immunoblot analyses showed that Survivin and XIAP expression were downregulated in emodin and the combination groups compared to the other two groups. Reverse transcriptase polymerase chain reaction analyses showed that Survivin and XIAP mRNA expression in emodin and the combination groups were downregulated significantly compared to the other two groups. Furthermore, the expression of the nuclear transcription factor κB (NF-κB) protein and NF-κB mRNA were downregulated in the emodin and the combination groups. DNA-binding activity of NF-κB was inhibited in emodin and combination groups compared to the other groups. This study suggests that emodin potentiates the antitumor effects of gemcitabine in PANC-1 cell xenografts via promotion of apoptosis and IAP suppression.
Journal Cover

June 2012
Volume 40 Issue 6

Print ISSN: 1019-6439
Online ISSN:1791-2423

2012 Impact Factor: 2.657
Ranked #31/196 Oncology
(total number of cites)

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APA
Guo, H., Guo, H., Bu, H., Bu, H., Luo, J., Luo, J., Wei, W., Wei, W., Liu, D., Liu, D., Chen, H., Chen, H., Tong, H., Tong, H., Wang, Z., Wang, Z., Wu, H., Wu, H., Li, H., Li, H., Zuo, M., Zuo, M., Li, W., Li, W., Lin, S., & Lin, S. (2012). Emodin potentiates the antitumor effects of gemcitabine in PANC-1 pancreatic cancer xenograft model in vivo via inhibition of inhibitors of apoptosis. International Journal of Oncology, 40(6), 1849-1857.
MLA
Guo, Guo, Bu, Bu, Luo, Luo, Wei, Wei, Liu, Liu, Chen, Chen, Tong, Tong, Wang, Wang, Wu, Wu, Li, Li, Zuo, Zuo, Li, Li, Lin, and Sheng-Zhang Lin. "Emodin potentiates the antitumor effects of gemcitabine in PANC-1 pancreatic cancer xenograft model in vivo via inhibition of inhibitors of apoptosis." International Journal of Oncology International Journal of Oncology 40.6 (2012): 1849-1857.
Chicago
Guo, Guo, Bu, Bu, Luo, Luo, Wei, Wei, Liu, Liu, Chen, Chen, Tong, Tong, Wang, Wang, Wu, Wu, Li, Li, Zuo, Zuo, Li, Li, Lin, and Sheng-Zhang Lin. "Emodin potentiates the antitumor effects of gemcitabine in PANC-1 pancreatic cancer xenograft model in vivo via inhibition of inhibitors of apoptosis." International Journal of Oncology International Journal of Oncology 40 no. 6 (2012): 1849-1857.