Krifa Mounira, El Meshri Salah Edin, Bentouati Nawel, Pizzi Antonio, Sick Emilie, Chekir-Ghedira Leila, Rondé Philippe
Unité de substances naturelles bioactives et biotechnologie UR12ES12, Faculté de pharmacie de Monastir, Tunisie.
UMR CNRS 7213, Laboratoire de Biophotonique et Pharmacologie, Université de Strasbourg, Faculté de Pharmacie, 74 route du Rhin, 67401, Illkirch, France.
J Cell Biochem. 2016 May;117(5):1167-75. doi: 10.1002/jcb.25400. Epub 2015 Oct 18.
A large number of plants used in traditional medicines have been shown to possess antitumor activities. The aims of this study were to evaluate any anticancer effect of the essential oil (EO) extracted from P. tortuosus against B16F10 melanoma cancer cells in vitro as well as in vivo. In vitro, EO was shown to induce apoptosis and to inhibit migration and invasion processes. Further investigation revealed that EO decreased focal adhesion and invadopodia formation which was accompanied by a drastic downregulation of FAK, Src, ERK, p130Cas and paxillin. Moreover, EO treatment decreased the expression level of p190RhoGAP, and Grb2, which impair cell migration and actin assembly. Mice bearing the melanoma cells were used to confirm any in vivo effectiveness of the EO as an anti-tumor promoting agent. In mice dosed with 100 mg EO/kg/d (for 27 days), tumor weight was inhibited by 98% compared to that in mice that did not receive the product. In conclusion, these data suggested to us that an EO of P. tortuosus could evolve to be a potential medicinal resource for use in the treatment of cancers.
大量用于传统医学的植物已被证明具有抗肿瘤活性。本研究的目的是评估从扭鞘香茶菜中提取的精油(EO)在体外和体内对B16F10黑色素瘤癌细胞的抗癌作用。在体外,EO被证明可诱导细胞凋亡,并抑制迁移和侵袭过程。进一步研究表明,EO可减少粘着斑和侵袭伪足的形成,同时伴随着粘着斑激酶(FAK)、Src、细胞外信号调节激酶(ERK)、p130Cas和桩蛋白的显著下调。此外,EO处理降低了p190RhoGAP和Grb2的表达水平,这两者会损害细胞迁移和肌动蛋白组装。携带黑色素瘤细胞的小鼠被用于确认EO作为抗肿瘤促进剂的体内有效性。在给予100mg EO/kg/d(持续27天)的小鼠中,与未接受该产品的小鼠相比,肿瘤重量受到了98%的抑制。总之,这些数据向我们表明,扭鞘香茶菜的EO可能会发展成为一种用于治疗癌症的潜在药物资源。