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Differential effect of intraperitoneal albendazole and paclitaxel on ascites formation and expression of vascular endothelial growth factor in ovarian cancer cell-bearing athymic nude mice.

DC Field Value Language
dc.contributor.author남은지-
dc.contributor.author임가원-
dc.contributor.author강명화-
dc.contributor.author김상운-
dc.contributor.author김영태-
dc.date.accessioned2014-12-20T17:53:21Z-
dc.date.available2014-12-20T17:53:21Z-
dc.date.issued2011-
dc.identifier.issn1933-7191-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/95447-
dc.description.abstractOBJECTIVES: The purposes of our study were to evaluate the effect of intraperitoneal albendazole on tumor growth, ascites formation, and vascular endothelial growth factor (VEGF) mRNA expression, and to assess the synergistic effect of paclitaxel in OVCAR-3-bearing nude mice. METHODS: In all, 4 groups of mice were injected intraperitoneally with weekly albendazole (450 mg/kg per week), paclitaxel (30 mg/kg per week), albendazole plus paclitaxel, or normal saline for 4 weeks. RESULTS: Ascitic fluid accumulation (2.47, 2.65, 2.88, and 5.90 mL, respectively) and in ascitic VEGF levels were significantly reduced in the 3 treatment groups compared to the control group (170.83, 229.16, 267, and 1625 pg/mL, respectively). However, complete tumor suppression was more prominent in the paclitaxel group, and VEGF mRNA expression was more strongly inhibited in the albendazole group (P < .05). No synergistic effect of albendazole and paclitaxel was observed. CONCLUSION: We demonstrated a differential effect of albendazole and paclitaxel in a xenograft model of ovarian carcinoma; albendazole suppressed ascites formation by inhibiting VEGF secretion, and paclitaxel exerted its effects by direct cytotoxicity.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfREPRODUCTIVE SCIENCES-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAlbendazole/administration & dosage-
dc.subject.MESHAnimals-
dc.subject.MESHAntineoplastic Agents, Phytogenic/administration & dosage-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols/pharmacology*-
dc.subject.MESHAscites/metabolism-
dc.subject.MESHFemale-
dc.subject.MESHMice-
dc.subject.MESHMice, Nude-
dc.subject.MESHOvarian Neoplasms/drug therapy*-
dc.subject.MESHOvarian Neoplasms/genetics-
dc.subject.MESHOvarian Neoplasms/metabolism-
dc.subject.MESHPaclitaxel/administration & dosage-
dc.subject.MESHRNA, Messenger/biosynthesis-
dc.subject.MESHRNA, Messenger/genetics-
dc.subject.MESHReverse Transcriptase Polymerase Chain Reaction-
dc.subject.MESHTubulin Modulators/administration & dosage-
dc.subject.MESHVascular Endothelial Growth Factor A/biosynthesis*-
dc.subject.MESHVascular Endothelial Growth Factor A/genetics-
dc.titleDifferential effect of intraperitoneal albendazole and paclitaxel on ascites formation and expression of vascular endothelial growth factor in ovarian cancer cell-bearing athymic nude mice.-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentYonsei Biomedical Research Center (연세의생명연구원)-
dc.contributor.googleauthorEun-Kyoung Choi-
dc.contributor.googleauthorSang-Wun Kim-
dc.contributor.googleauthorEun-Ji Nam-
dc.contributor.googleauthorJiheum Pa다-
dc.contributor.googleauthorGa-Won Yim-
dc.contributor.googleauthorMyeong-Hwa Kang-
dc.contributor.googleauthorYoung-Tae Kim-
dc.identifier.doi10.1177/1933719111398142-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA04147-
dc.contributor.localIdA01262-
dc.contributor.localIdA03354-
dc.contributor.localIdA00020-
dc.contributor.localIdA00526-
dc.contributor.localIdA00729-
dc.relation.journalcodeJ02606-
dc.identifier.eissn1933-7205-
dc.identifier.pmid21421899-
dc.identifier.urlhttp://rsx.sagepub.com/content/18/8/763-
dc.subject.keywordalbendazole-
dc.subject.keywordpaclitaxel-
dc.subject.keywordascites-
dc.subject.keywordvascular endothelial growth factor-
dc.subject.keywordovarian carcinoma-
dc.contributor.alternativeNameNam, Eun Ji-
dc.contributor.alternativeNameYim, Ga Won-
dc.contributor.alternativeNameChoi, Eun Kyoung-
dc.contributor.alternativeNameKang, Myung Hwa-
dc.contributor.alternativeNameKim, Sang Wun-
dc.contributor.alternativeNameKim, Young Tae-
dc.contributor.affiliatedAuthorChoi, Eun Kyoung-
dc.contributor.affiliatedAuthorNam, Eun Ji-
dc.contributor.affiliatedAuthorYim, Ga Won-
dc.contributor.affiliatedAuthorKang, Myung Hwa-
dc.contributor.affiliatedAuthorKim, Sang Wun-
dc.contributor.affiliatedAuthorKim, Young Tae-
dc.rights.accessRightsnot free-
dc.citation.volume18-
dc.citation.number8-
dc.citation.startPage763-
dc.citation.endPage771-
dc.identifier.bibliographicCitationREPRODUCTIVE SCIENCES, Vol.18(8) : 763-771, 2011-
dc.identifier.rimsid40822-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Obstetrics and Gynecology (산부인과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers

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