Osteosarcoma Phenotype Is Inhibited by 3,4-Methylenedioxy-β-nitrostyrene.

Sarcoma

Department of Orthopaedics, University Hospitals Case Medical Center, Case Western Reserve University, 11100 Euclid Avenue, Cleveland, OH 44106, USA.

Published: August 2012

AI Article Synopsis

  • β-nitrostyrene compounds like 3,4-methylenedioxy-β-nitrostyrene (MNS) have shown potential in inhibiting tumor growth and inducing cell death, but their effects on osteosarcoma specifically were previously unexplored.
  • In experiments with different osteosarcoma cell lines, MNS significantly reduced cell motility by 72-76% and colony formation by 95-100%, while also disrupting existing colonies in a time- and dose-dependent manner.
  • MNS affected human osteoblasts similarly, indicating potential therapeutic benefits, while it had little impact on airway epithelial cells, highlighting the specificity of MNS's effects.

Article Abstract

β-nitrostyrene compounds, such as 3,4-methylenedioxy-β-nitrostyrene (MNS), inhibit growth and induce apoptosis in tumor cells, but no reports have investigated their role in osteosarcoma. In this study, human osteosarcoma cell families with cell lines of varying tumorigenic and metastatic potential were utilized. Scrape motility assays, colony formation assays, and colony survival assays were performed with osteosarcoma cell lines, both in the presence and absence of MNS. Effects of MNS on human osteoblasts and airway epithelial cells were assessed in monolayer cultures. MNS decreased metastatic cell line motility by 72-76% and colony formation by 95-100%. MNS consistently disrupted preformed colonies in a time-dependent and dose-dependent manner. MNS had similar effects on human osteoblasts but little effect on airway epithelial cells. An inactive analog of MNS had no detectable effects, demonstrating specificity. MNS decreases motility and colony formation of osteosarcoma cells and disrupts preformed cell colonies, while producing little effect on pulmonary epithelial cells.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3371351PMC
http://dx.doi.org/10.1155/2012/479712DOI Listing

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