1. Academic Validation
  2. Oxyprenylated Phenylpropanoids Bind to MT1 Melatonin Receptors and Inhibit Breast Cancer Cell Proliferation and Migration

Oxyprenylated Phenylpropanoids Bind to MT1 Melatonin Receptors and Inhibit Breast Cancer Cell Proliferation and Migration

  • J Nat Prod. 2017 Dec 22;80(12):3324-3329. doi: 10.1021/acs.jnatprod.7b00853.
Mahmud Hasan 1 Salvatore Genovese 2 Serena Fiorito 2 Francesco Epifano 2 Paula A Witt-Enderby 1
Affiliations

Affiliations

  • 1 Division of Pharmaceutical, Administrative and Social Sciences, Duquesne University , Pittsburgh, Pennsylvania 15282, United States.
  • 2 Department of Pharmacy, University "G. d'Annunzio" of Chieti e Pescara , Chieti 66100, Italy.
Abstract

Oxyprenylated compounds (i.e., ferulic acid and coumarin derivatives) demonstrate neuroprotection and Anticancer properties as reported in previous studies. We have tested the affinity of oxyprenylated ferulic acid (1-4) and umbelliferone derivatives (5-11) to melatonin receptors as well as their antiproliferation and antimigratory properties against breast Cancer (BC) cell lines. All the compounds except for ferulic acid, boropinic acid, and umbelliferone had binding affinities to melatonin receptors in the nM to μM range, and both auraptene and umbellinprenin reduced BC cell proliferation and migration in phenotypically diverse BC including triple negative.

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