Abstract | BACKGROUND: 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:
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Authors | Reza F Saidi, Ahmad Ahad, Jacqueline Tilak, Ilke Nalbantoglu, Michael J Jacobs |
Journal | The Journal of surgical research
(J Surg Res)
Vol. 173
Issue 2
Pg. 309-13
(Apr 2012)
ISSN: 1095-8673 [Electronic] United States |
PMID | 21067774
(Publication Type: Journal Article)
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Copyright | Copyright © 2012 Elsevier Inc. All rights reserved. |
Chemical References |
- Antimetabolites, Antineoplastic
- Immunologic Factors
- Interferon-alpha
- Deoxycytidine
- Receptor, Interferon alpha-beta
- Gemcitabine
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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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