Cited by 100Angiogenesis and VEGF in CancerIntraperitoneal and Appendiceal MalignanciesOvarian cancer diagnosis and treatment

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Albendazole: a Potent Inhibitor of Vascular Endothelial Growth Factor and Malignant Ascites Formation in OVCAR-3 Tumor-Bearing Nude Mice

Hossein Pourgholami, Mohammad, Yan Cai, Zhao, Lu, Ying, Wang, Lisa, Lawson Morris, David·2006·Clinical Cancer Research

Abstract

Purpose: Angiogenesis and vessel hyperpermeability are the two factors leading to the formation of ascites. Vascular endothelial growth factor (VEGF) plays a pivotal role in malignant ascites formation. We have recently shown that albendazole inhibits peritoneal growth of human colorectal cancer cells (HT-29). The present study was designed to find out if albendazole can suppress ascites formation in ascites-producing peritoneal carcinomatosis. Experimental design: Female nude mice bearing peritoneal tumors of human ovarian cancer cells (OVCAR-3) were treated with albendazole. Following i.p. inoculation and ascites development, mice were given i.p. albendazole (150 mg/kg) or the vehicle × 3 weekly for 4 weeks. Results: Whereas vehicle-treated mice developed overt ascites requiring repeated aspiration, ascites formation in the albendazole-treated mice was markedly suppressed. As a result of this, 7 of 10 mice from the control group had to be euthanized before the course of treatment was over. Suppressed ascites production and reduced tumor vascularity observed was a result of dramatic reduction in tumor VEGF production as revealed by profoundly lower VEGF ascites fluid and plasma levels. In vitro, incubation of SKOV-3 cells with various concentrations of albendazole led to significant dose-dependent inhibition of VEGF secretion. Examination of floating tumor cells collected from the peritoneal wash revealed profound down-regulation of VEGF mRNA in albendazole-treated mice. Conclusions: These findings suggest for the first time that in nude mice bearing OVCAR-3 peritoneal tumors, by inhibiting VEGF production, albendazole abolishes tumor angiogenesis and ascites formation.

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Metadata

Authors
Hossein Pourgholami, M., Yan Cai, Z., Lu, Y., Wang, L., & Lawson Morris, D.
Affiliations
  • Authors' Affiliation: Cancer Research Laboratories, Department of Surgery, St. George Hospital, University of New South Wales, Sydney, New South Wales, Australia
  • UNSW Sydney (AU)
Venue
Clinical Cancer Research
Published
2006-03-15
Volume
12
Issue
6
Pages
1928-1935
ISSN
  • 1078-0432 (ISSN-L)
  • 1557-3265
OpenAlex
W2115847666
Cited by
100
References
1
Citations by year
2026: 1 · 2025: 2 · 2024: 2 · 2023: 4 · 2022: 3 · 2021: 8 · 2020: 7 · 2019: 2 · 2018: 2 · 2017: 8 · 2016: 5 · 2015: 8 · 2014: 4 · 2013: 8 · 2012: 8
FWCI
1.90
Type
journal article
Language
en
Open access
closed
Locations
  • Clinical Cancer Research (publishedVersion)
  • PubMed (publishedVersion)
Funders
University of New South Wales
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
  • Health Sciences › Medicine › Surgery › Intraperitoneal and Appendiceal Malignancies
  • Health Sciences › Medicine › Oncology › Ovarian cancer diagnosis and treatment
Keywords
albendazole, vascular endothelial growth factor, malignant ascites, ovarian cancer, peritoneal carcinomatosis, tumor angiogenesis, VEGF inhibition, OVCAR-3 cells, SKOV3 cells, nude mice
MeSH terms
Animals, Ascites, Female, Humans, Injections, Intraperitoneal, Mice, Inbred BALB C, Mice, Nude, Neovascularization, Pathologic, Ovarian Neoplasms, RNA, Messenger, Albendazole, Gene Expression, CA-125 Antigen, Protein Isoforms, Reverse Transcriptase Polymerase Chain Reaction, Xenograft Model Antitumor Assays, Vascular Endothelial Growth Factor A, Cell Line, Tumor, Cell Proliferation, Mice

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