4.7 Article

Oxidized Products of α-Linolenic Acid Negatively Regulate Cellular Survival and Motility of Breast Cancer Cells

期刊

BIOMOLECULES
卷 10, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/biom10010050

关键词

phytoprostane; breast cancer; lipids

资金

  1. Le Studium (Region Centre-Val de Loire, France)
  2. INCa PLBio [2018-145]
  3. Lipids ARD2020-Biodrug project (Region Centre-Val de Loire, France)
  4. La Ligue contre le Cancer (Indre et Loire)
  5. La Ligue contre le Cancer (Loir et Cher)
  6. La Ligue contre le Cancer (Vienne)
  7. Region Centre-Val de Loire (France)
  8. Canceropole Grand-Ouest (Mature project)

向作者/读者索取更多资源

Despite recent advances in our understanding of the biological processes leading to the development and progression of cancer, there is still a need for new and effective agents to treat this disease. Phytoprostanes (PhytoPs) and phytofurans (PhytoFs) are non-enzymatically oxidized products of alpha-linolenic acid that are present in seeds and vegetable oils. They have been shown to possess anti-inflammatory and apoptosis-promoting activities in macrophages and leukemia cells, respectively. In this work, seven PhytoPs (PP1-PP7) and one PhytoFs (PF1) were evaluated for their cytotoxic, chemosensitization, and anti-migratory activities using the MCF-7 and MDA-MB-231 breast cancer cell lines. Among the tested compounds, only three PhytoPs had a significant effect on cell viability compared to the control group: Ent-9-L-1-PhytoP (PP6) decreased cell viability in both cell lines, while 16-F-1t-PhytoP (PP1) and 9-L-1-PhytoP (PP5) decreased viability of MCF-7 and MDA-MB-231 cells, respectively. When combined with a sub-cytotoxic dose of doxorubicin, these three PhytoPs displayed significantly enhanced cytotoxic effects on MCF-7 cells while the chemotherapeutic drug alone had no effect. In cellular motility assays, Ent-9-(RS)-12-epi-ST-Delta(10)-13-PhytoF could significantly inhibit cellular migration of MDA-MB-231 cells. In addition, Ent-9-(RS)-12-epi-ST-Delta(10)-13-PhytoF also enhanced cellular adhesion of MDA-MB-231 cells.

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