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FDG-PET for evaluating the antitumor effect of intraarterial 3-bromopyruvate administration in a rabbit VX2 liver tumor model

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dc.contributor.author강원준-
dc.date.accessioned2014-12-21T17:09:55Z-
dc.date.available2014-12-21T17:09:55Z-
dc.date.issued2007-
dc.identifier.issn1229-6929-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/97068-
dc.description.abstractObjective We wanted to investigate the feasibility of using FDG-PET for evaluating the antitumor effect of intraarterial administration of a hexokinase II inhibitor, 3-bromopyruvate (3-BrPA), in a rabbit VX2 liver tumor model. Materials and Methods VX2 carcinoma was grown in the livers of ten rabbits. Two weeks later, liver CT was performed to confirm appropriate tumor growth for the experiment. After tumor volume-matched grouping of the rabbits, transcatheter intraarterial administration of 3-BrPA was performed (1 mM and 5 mM in five animals each, respectively). FDG-PET scan was performed the day before, immediately after and a week after 3-BrPA administration. FDG uptake was semiquantified by measuring the standardized uptake value (SUV). A week after treatment, the experimental animals were sacrificed and the necrosis rates of the tumors were calculated based on the histopathology. Results The SUV of the VX2 tumors before treatment (3.87 ±1.51 [mean ±SD]) was significantly higher than that of nontumorous liver parenchyma (1.72 ±0.34) (p < 0.0001, Mann-Whitney U test). The SUV was significantly decreased immediately after 3-BrPA administration (2.05 ±1.21) (p = 0.002, Wilcoxon signed rank test). On the one-week follow up PET scan, the FDG uptake remained significantly lower (SUV 1.41 ±0.73) than that before treatment (p = 0.002), although three out of ten animals showed a slightly increasing tendency for the FDG uptake. The tumor necrosis rate ranged from 50.00% to 99.90% (85.48% ±15.87). There was no significant correlation between the SUV or the SUV decrease rate and the tumor necrosis rate in that range. Conclusion Even though FDG-PET cannot exactly reflect the tumor necrosis rate, FDG-PET is a useful modality for the early assessment of the antitumor effect of intraarterial administration of 3-BrPA in VX2 liver tumor.-
dc.description.statementOfResponsibilityopen-
dc.format.extent216~224-
dc.relation.isPartOfKOREAN JOURNAL OF RADIOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleFDG-PET for evaluating the antitumor effect of intraarterial 3-bromopyruvate administration in a rabbit VX2 liver tumor model-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Nuclear Medicine (핵의학)-
dc.contributor.googleauthorHee Sun Park-
dc.contributor.googleauthorJin Wook Chung-
dc.contributor.googleauthorKichang Lee-
dc.contributor.googleauthorJung Hwan Yoon Hesson Chung-
dc.contributor.googleauthorWon Jun Kang-
dc.contributor.googleauthorJae Hyung Park-
dc.contributor.googleauthorMin Jong Lee-
dc.contributor.googleauthorKyu Ri Son-
dc.contributor.googleauthorYoung Il Kim-
dc.contributor.googleauthorHwan Jun Jae-
dc.identifier.doi10.3348/kjr.2007.8.3.216-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00062-
dc.relation.journalcodeJ02884-
dc.identifier.eissn2005-8330-
dc.contributor.alternativeNameKang, Won Jun-
dc.contributor.affiliatedAuthorKang, Won Jun-
dc.rights.accessRightsfree-
dc.citation.volume8-
dc.citation.number3-
dc.citation.startPage216-
dc.citation.endPage224-
dc.identifier.bibliographicCitationKOREAN JOURNAL OF RADIOLOGY, Vol.8(3) : 216-224, 2007-
dc.identifier.rimsid53642-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Nuclear Medicine (핵의학교실) > 1. Journal Papers

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