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Anti-tumour potential and selectivity of caffeic acid phenethyl ester in osteosarcoma cells.

Abstract
Osteosarcoma is the most common type of bone cancer, and metastasis is widespread decreasing the survival rate. The search for new therapeutic strategies has increased for phytochemicals due to their potential as antioxidants and anticancer properties. Thus, we evaluated the caffeic acid phenethyl ester (CAPE) and caffeic acid's (CA) anticancer properties on UMR-106 murine osteosarcoma cells. The IC25 and IC50 were 1.3 and 2.7 μM for CAPE and 91.0 and 120.0 μM for CA, respectively. This study shows the potential anticancer properties of CAPE and highlights how a phenethyl ester component addition can improve the pharmacological potency in relation to its precursor CA. Our results showed that CAPE was more efficient and selective in reducing the viability of tumor cells compared to the control osteoblasts (MC3T3-E1) (p < 0.05). In addition, CAPE was 44-fold (IC25) and 70-fold (IC50) more cytotoxic than CA. CAPE also decreased ROS generation and cell migration. In summary, CAPE was more selective for tumor cells, preserving normal ones, suggesting its potential role as an anticancer drug.
AuthorsAna Lígia Pagnan, Adriano Souza Pessoa, Cintia Kazuko Tokuhara, Vanessa Svizzero Fakhoury, Gabriela Silva Neubern Oliveira, Mariana Liessa Rovis Sanches, Kelly Karina Inacio, Valdecir Farias Ximenes, Rodrigo Cardoso Oliveira
JournalTissue & cell (Tissue Cell) Vol. 74 Pg. 101705 (Feb 2022) ISSN: 1532-3072 [Electronic] Scotland
PMID34864499 (Publication Type: Journal Article)
CopyrightCopyright © 2021 Elsevier Ltd. All rights reserved.
Chemical References
  • Antineoplastic Agents
  • Caffeic Acids
  • caffeic acid phenethyl ester
  • Phenylethyl Alcohol
Topics
  • Animals
  • Antineoplastic Agents (pharmacology)
  • Bone Neoplasms (drug therapy, metabolism, pathology)
  • Caffeic Acids (pharmacology)
  • Cell Line, Tumor
  • Cell Movement (drug effects)
  • Cell Proliferation (drug effects)
  • Cell Survival (drug effects)
  • Mice
  • Osteosarcoma (drug therapy, metabolism, pathology)
  • Phenylethyl Alcohol (analogs & derivatives, pharmacology)

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