BACKGROUND: Sesquiterpene lactones (SL) are plant secondary metabolites that are known for their anti-fungal, anti-bacterial, anti-inflammatory, and anti-tumor properties. Considering that several SL-derived drugs are currently in cancer clinical trials, we have tested two SL molecules, 3-β-methoxy-iso-seco-tanapartholide (β-tan) isolated from Achillea falcata and salograviolide A (Sal A) isolated from Centaurea ainetensis, for their anti-tumor properties. We used the mouse epidermal JB6Pâ+âcells as a model for tumor promotion and cellular transformation. Key players that are involved in cellular transformation and tumorigenesis are the AP-1 and NF-κB transcription factors; therefore, we assessed how β-tan and Sal A modulate their signaling pathways in JB6Pâ+âcells. METHODS: The effects of β-tan and Sal A on the growth of normal and neoplastic keratinocytes and on the tumor promotion-responsive JB6Pâ+âcells were determined using the MTT assay. Anchorage-independent cell growth transformation assays were used to evaluate the anti-tumor promoting properties of these SL molecules in JB6Pâ+âcells and dual luciferase reporter assays and western blot analysis were used to investigate their effects on tumor promoter-induced AP-1 and NF-κB activities and protein levels of key AP-1 and NF-кB target genes. RESULTS: β-tan and Sal A selectively inhibited tumor promoter-induced cell growth and transformation of JB6Pâ+âcells at concentrations that do not affect JB6Pâ+âand primary keratinocytes basal cell growth. In addition, both molecules reduced basal and tumor promoter-induced NF-κB transcriptional activities, differentially regulated basal and tumor promoter-induced AP-1 transcriptional activities, and modulated key players of the AP-1 and NF-κB signaling pathways. CONCLUSIONS: These results highlight the anti-tumor promoting properties of β-tan and Sal A. These SL molecules isolated from two plant species native to the Middle East may provide opportunities for complementary medicine practices.
Sesquiterpene lactones isolated from indigenous Middle Eastern plants inhibit tumor promoter-induced transformation of JB6 cells.
从中东本土植物中分离出的倍半萜内酯可抑制肿瘤促进剂诱导的 JB6 细胞转化
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作者:Saikali Melody, Ghantous Akram, Halawi Racha, Talhouk Salma N, Saliba Najat A, Darwiche Nadine
| 期刊: | BMC Complementary and Alternative Medicine | 影响因子: | 3.400 |
| 时间: | 2012 | 起止号: | 2012 Jul 9; 12:89 |
| doi: | 10.1186/1472-6882-12-89 | 研究方向: | 肿瘤 |
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