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The expression of interferon receptor α/β in human pancreatic cancer in nude mice is essential for tumor response to interferon α treatment.

AbstractBACKGROUND:
Adjuvant interferon based chemoradiation has rendered promising results against pancreatic cancer. This study evaluated the in vivo effect of interferon α on two human pancreatic carcinoma cell lines implanted in nude.
MATERIAL AND METHODS:
MiaPaCa-2 expressed the interferon α/β receptor and Panc-1 cells did not. Regimen I consisted of intraperitoneal single-agent gemcitabine and Regimen II consisted of IFN-α and gemcitabine biweekly for 30 d.
RESULTS:
Regimen I and II significantly decreased median tumor volume compared with control mice (P < 0.001). However, MiaPaCa-2 showed a more dramatic response to Regimen II compared with Panc-1 implanted mice. MiaPaCa-2 and treated with Regimen II showed less metastasis and less local invasion compared with Panc-1 treated with same regimen. Regimen II was more effective on MiaPaCa-2 compared with Regimen I (P < 0.001). There were no differences between Regimens I and II in the Panc-1 group.
CONCLUSIONS:
Treatment of human pancreatic cancer in nude mice with interferon α and gemcitabine was associated with a reduction in tumor volume. This process was more prominent in the cells that express the interferon receptors.
AuthorsReza F Saidi, Ahmad Ahad, Jacqueline Tilak, Ilke Nalbantoglu, Michael J Jacobs
JournalThe Journal of surgical research (J Surg Res) Vol. 173 Issue 2 Pg. 309-13 (Apr 2012) ISSN: 1095-8673 [Electronic] United States
PMID21067774 (Publication Type: Journal Article)
CopyrightCopyright © 2012 Elsevier Inc. All rights reserved.
Chemical References
  • Antimetabolites, Antineoplastic
  • Immunologic Factors
  • Interferon-alpha
  • Deoxycytidine
  • Receptor, Interferon alpha-beta
  • Gemcitabine
Topics
  • Animals
  • Antimetabolites, Antineoplastic (therapeutic use)
  • Carcinoma (drug therapy, metabolism)
  • Cell Line, Tumor
  • Deoxycytidine (analogs & derivatives, therapeutic use)
  • Humans
  • Immunologic Factors (therapeutic use)
  • Interferon-alpha (therapeutic use)
  • Male
  • Mice
  • Mice, Nude
  • Pancreatic Neoplasms (drug therapy, metabolism)
  • Receptor, Interferon alpha-beta (metabolism)
  • Gemcitabine

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