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Radioimmunotherapy of pancreatic cancer xenografts in nude mice using 90Y-labeled anti-α6β4 integrin antibody.
- Source :
-
Oncotarget [Oncotarget] 2016 Jun 21; Vol. 7 (25), pp. 38835-38844. - Publication Year :
- 2016
-
Abstract
- The contribution of integrin α6β4 (α6β4) overexpression to the pancreatic cancer invasion and metastasis has been previously shown. We have reported immunotargeting of α6β4 for radionuclide-based and near-infrared fluorescence imaging in a pancreatic cancer model. In this study, we prepared yttrium-90 labeled anti-α6β4 antibody (90Y-ITGA6B4) and evaluated its radioimmunotherapeutic efficacy against pancreatic cancer xenografts in nude mice. Mice bearing xenograft tumors were randomly divided into 5 groups: (1) single administration of 90Y-ITGA6B4 (3.7MBq), (2) double administrations of 90Y-ITGA6B4 with once-weekly schedule (3.7MBq x 2), (3) single administration of unlabeled ITGA6B4, (4) double administrations of unlabeled ITGA6B4 with once-weekly schedule and (5) the untreated control. Biweekly tumor volume measurements and immunohistochemical analyses of tumors at 2 days post-administration were performed to monitor the response to treatments. To assess the toxicity, body weight was measured biweekly. Additionally, at 27 days post-administration, blood samples were collected through cardiac puncture, and hematological parameters, hepatic and renal functions were analyzed. Both 90Y-ITGA6B4 treatment groups showed reduction in tumor volumes (P < 0.04), decreased cell proliferation marker Ki-67-positive cells and increased DNA damage marker p-H2AX-positive cells, compared with the other groups. Mice treated with double administrations of 90Y-ITGA6B4, exhibited myelosuppression. There were no significant differences in hepatic and renal functions between the 2 treatment groups and the other groups. Our results suggest that 90Y-ITGA6B4 is a promising radioimmunotherapeutic agent against α6β4 overexpressing tumors. In the future studies, dose adjustment for fractionated RIT should be considered carefully in order to get the optimal effect while avoiding myelotoxicity.<br />Competing Interests: The authors declare no other potential conflicts of interest relevant to this article exist.
- Subjects :
- Animals
Antibodies, Monoclonal chemistry
Body Weight
Cell Line, Tumor
Female
Fluorodeoxyglucose F18 chemistry
Humans
Mice
Mice, Inbred BALB C
Mice, Nude
Neoplasm Transplantation
Pancreatic Neoplasms immunology
Positron-Emission Tomography
Tissue Distribution
Transplantation, Heterologous
Tumor Cells, Cultured
Xenograft Model Antitumor Assays
Antibodies, Monoclonal pharmacology
Integrin alpha6beta4 chemistry
Pancreatic Neoplasms radiotherapy
Radioimmunotherapy methods
Yttrium Radioisotopes chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1949-2553
- Volume :
- 7
- Issue :
- 25
- Database :
- MEDLINE
- Journal :
- Oncotarget
- Publication Type :
- Academic Journal
- Accession number :
- 27246980
- Full Text :
- https://doi.org/10.18632/oncotarget.9631