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Antiangiogenic, antimigratory and antiinflammatory effects of 2-methoxyestradiol in zebrafish larvae

  • Marisol Quezada
  • , Marjorie Alvarez
  • , Oscar A. Peña
  • , Soledad Henríquez
  • , Claudia A. D'Alençon
  • , Soledad Lange
  • , Barbara Oliva
  • , Gareth I. Owen
  • , Miguel L. Allende*
  • *Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

20 Citations (Scopus)

Abstract

2-Methoxyestradiol (2ME), an endogenous metabolite of 17β-estradiol, has been previously reported to possess antiangiogenic and antitumor properties. Herein, we demonstrate that the effects of this antiangiogenic steroid can be readily assayed in live zebrafish, introducing a convenient and robust new model system as a screening tool for both single cell and collective cell migration assays. Using the in vitro mammalian endothelial cell line EA.hy926, we first show that cell migration and angiogenesis, as estimated by wound assay and tube formation respectively, are antagonized by 2ME. In zebrafish (Danio rerio) larvae, dose-dependent exposure to 2ME diminishes (1) larval angiogenesis, (2) leukocyte recruitment to damaged lateral line neuromasts and (3) retards the lateral line primordium in its migration along the body. Our results indicate that 2ME has an effect on collective cell migration in vivo as well as previously reported anti-tumorigenic activity and suggests that the molecular mechanisms governing cell migration in a variety of contexts are conserved between fish and mammals. Moreover, we exemplify the versatility of the zebrafish larvae for testing diverse physiological processes and screening for antiangiogenic and antimigratory drugs in vivo.

Original languageEnglish
Pages (from-to)141-149
Number of pages9
JournalComparative Biochemistry and Physiology - C Toxicology and Pharmacology
Volume157
Issue number2
DOIs
Publication statusPublished - Mar 2013

Bibliographical note

Funding Information:
We thank Florencio Espinoza and Catalina Lafourcade for technical help and animal husbandry. The following colleagues kindly provided transgenic zebrafish lines: Darren Gilmour, Steve Renshaw, Herwig Baier and Brant Weinstein. GIO was supported by the BRMC CTU06. MA was supported by grants from FONDAP ( 15090007 ) and ICGEB ( CRP/CHI11-01 ).

Keywords

  • 2-methoxyestradiol
  • Angiogenesis
  • EA.hy926
  • Inflammation
  • Neutrophil migration
  • Primordium
  • Zebrafish

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