Early Monitoring Antiangiogenesis Treatment Response of Sunitinib in U87MG Tumor Xenograft by 18F-FLT MicroPET/CT Imaging

Aim. It was aimed to monitor early treatment response of Sunitinib in U87MG models mimicking glioblastoma multiforme by longitudinal 18F-FLT microPET/CT imaging in this study. Methods. U87MG tumor mice were intragastrically injected with Sunitinib at a dose of 80 mg/kg for consecutive 7 days. 18F-FL...

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Main Authors: Xiao Bao, Ming-Wei Wang, Yong-Ping Zhang, Ying-Jian Zhang
Format: Article
Language:English
Published: Hindawi Limited 2014-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2014/218578
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spelling doaj-93e43b9056ad4485b2a2ad6e13187ae02020-11-24T20:59:05ZengHindawi LimitedBioMed Research International2314-61332314-61412014-01-01201410.1155/2014/218578218578Early Monitoring Antiangiogenesis Treatment Response of Sunitinib in U87MG Tumor Xenograft by 18F-FLT MicroPET/CT ImagingXiao Bao0Ming-Wei Wang1Yong-Ping Zhang2Ying-Jian Zhang3Department of Nuclear Medicine, Fudan University Shanghai Cancer Center, Shanghai 200032, ChinaDepartment of Nuclear Medicine, Fudan University Shanghai Cancer Center, Shanghai 200032, ChinaDepartment of Nuclear Medicine, Fudan University Shanghai Cancer Center, Shanghai 200032, ChinaDepartment of Nuclear Medicine, Fudan University Shanghai Cancer Center, Shanghai 200032, ChinaAim. It was aimed to monitor early treatment response of Sunitinib in U87MG models mimicking glioblastoma multiforme by longitudinal 18F-FLT microPET/CT imaging in this study. Methods. U87MG tumor mice were intragastrically injected with Sunitinib at a dose of 80 mg/kg for consecutive 7 days. 18F-FLT microPET/CT scans were acquired on days 0, 1, 3, 7, and 13 after therapy. Tumor sizes and body weight were measured. Tumor samples were collected for immunohistochemical analysis of proliferation and microvessel density (MVD) with anti-Ki67 and anti-CD31, respectively. Results. The uptake ratios of tumor to the contralateral muscle (T/M) of 18F-FLT in the Sunitinib group decreased from baseline to day 3 (T/M0 = 2.98 ± 0.33; T/M3 = 2.23 ± 0.36; P<0.001), reached the bottom on day 7 (T/M7 = 1.96 ± 0.35; P<0.001), and then recovered on day 13. The T/M of 18F-FLT uptake in the control group remained around 3.0. There was no difference for the tumor size between both groups until day 11. 18F-FLT uptakes of tumor were correlated with Ki67 staining index and MVD. Conclusion. Early therapy response to Sunitinib could be predicted via 18F-FLT PET, which will contribute to monitoring antiangiogenesis treatment.http://dx.doi.org/10.1155/2014/218578
collection DOAJ
language English
format Article
sources DOAJ
author Xiao Bao
Ming-Wei Wang
Yong-Ping Zhang
Ying-Jian Zhang
spellingShingle Xiao Bao
Ming-Wei Wang
Yong-Ping Zhang
Ying-Jian Zhang
Early Monitoring Antiangiogenesis Treatment Response of Sunitinib in U87MG Tumor Xenograft by 18F-FLT MicroPET/CT Imaging
BioMed Research International
author_facet Xiao Bao
Ming-Wei Wang
Yong-Ping Zhang
Ying-Jian Zhang
author_sort Xiao Bao
title Early Monitoring Antiangiogenesis Treatment Response of Sunitinib in U87MG Tumor Xenograft by 18F-FLT MicroPET/CT Imaging
title_short Early Monitoring Antiangiogenesis Treatment Response of Sunitinib in U87MG Tumor Xenograft by 18F-FLT MicroPET/CT Imaging
title_full Early Monitoring Antiangiogenesis Treatment Response of Sunitinib in U87MG Tumor Xenograft by 18F-FLT MicroPET/CT Imaging
title_fullStr Early Monitoring Antiangiogenesis Treatment Response of Sunitinib in U87MG Tumor Xenograft by 18F-FLT MicroPET/CT Imaging
title_full_unstemmed Early Monitoring Antiangiogenesis Treatment Response of Sunitinib in U87MG Tumor Xenograft by 18F-FLT MicroPET/CT Imaging
title_sort early monitoring antiangiogenesis treatment response of sunitinib in u87mg tumor xenograft by 18f-flt micropet/ct imaging
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2014-01-01
description Aim. It was aimed to monitor early treatment response of Sunitinib in U87MG models mimicking glioblastoma multiforme by longitudinal 18F-FLT microPET/CT imaging in this study. Methods. U87MG tumor mice were intragastrically injected with Sunitinib at a dose of 80 mg/kg for consecutive 7 days. 18F-FLT microPET/CT scans were acquired on days 0, 1, 3, 7, and 13 after therapy. Tumor sizes and body weight were measured. Tumor samples were collected for immunohistochemical analysis of proliferation and microvessel density (MVD) with anti-Ki67 and anti-CD31, respectively. Results. The uptake ratios of tumor to the contralateral muscle (T/M) of 18F-FLT in the Sunitinib group decreased from baseline to day 3 (T/M0 = 2.98 ± 0.33; T/M3 = 2.23 ± 0.36; P<0.001), reached the bottom on day 7 (T/M7 = 1.96 ± 0.35; P<0.001), and then recovered on day 13. The T/M of 18F-FLT uptake in the control group remained around 3.0. There was no difference for the tumor size between both groups until day 11. 18F-FLT uptakes of tumor were correlated with Ki67 staining index and MVD. Conclusion. Early therapy response to Sunitinib could be predicted via 18F-FLT PET, which will contribute to monitoring antiangiogenesis treatment.
url http://dx.doi.org/10.1155/2014/218578
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