Cuprous oxide nanoparticles effect on the epithelial-mesenchymal transition of B16 cells
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摘要: 目的 制备氧化亚铜纳米粒(cuprous oxide nanoparticles,CONPs)并研究对小鼠黑色素瘤B16细胞上皮间质转化的影响。 方法 采用水热法制备氧化亚铜纳米粒。将B16细胞分为正常培养组和CONPs(5、25、50 μg/ml)刺激培养组,于倒置相差显微镜下观察细胞形态学的变化,通过细胞划痕实验和Transwell检测CONPs对B16细胞迁移能力的影响,采用免疫荧光染色法和蛋白质印迹法检测B16细胞表型的相关分子标志物表达的变化。 结果 合成的氧化亚铜纳米粒分布均匀,粒径约40 nm;体外细胞实验发现CONPs明显地抑制了B16细胞的迁移和侵袭能力;并刺激B16细胞上皮细胞表型的E-cadherin、Cytokeratin、Desmoplakin的表达明显升高,而间质细胞表型的N-cadherin、Vimentin的表达降低。 结论 CONPs能明显地抑制黑色素瘤细胞的侵袭转移和上皮-间质转化(EMT)过程。Abstract: Objective To research the epithelial-mesenchymal transition (EMT) effects of cuprous oxide nanoparticles (CONPs) on melanoma. Methods Cuprous oxide nanoparticles were prepared hydrothermally.The B16 cells were cultured with cuprous oxide nanoparticlesat different concentrations (5,25,50 μg/ml).The changes of the morphology of the B16 cell were observed under the inverted microscope.The effects of CONPs on B16 cell migration ability were detected through the Wound healing assay and the Transwell assay.Then cell immunofluorescence and western blotting were used to test the EMT related molecular markers, including E-cadherin, N-cadherin, Cytokeratin, and Vimentin. Results The synthesized cuprous oxide nanoparticles distribute uniformly with a diameter of 40 nm.Our study indicated that CONPs inhibited the EMT of B16 cell.A conversion process was discovered in this study.In B16 cells, CONPs inhibited B16 cell migration, promoted the expression of E-cadherin, Cytokeratin and Desmoplakin, while the expression of N-cadherin and Vimentin was repressed in protein level. Conclusion Cuprous oxide nanoparticles can significantly restrain the invasion and metastasis of melanoma cells and inhabit the EMT of B16 cells.
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[1] Wan L, Pantel K, Kang Y.Tumor metastasis: moving new biological insights into the clinic[J].Nat Med, 2013, 19(11):1450-1464. [2] Torzilli PA, Bourne JW, Cigler T, et al. A new paradigm for mechanobiological mechanisms in tumor metastasis[J].Semin Cancer Biol, 2012, 22(5-6):385-395.. [3] Rhim AD, Aiello NM, Mirek ET, et al.Abstract IA5: EMT and dissemination precede pancreatic tumor formation.[J].Cancer Res, 2014, 72(14 Supplement):IA5-IA5. [4] Thomas N.Seyfried, Huysentruyt LC.On the origin of cancer metastasis[J].Crit Rev Oncog, 2013, 18(1-2):43-73. [5] Foroni C, Broggini M, Generali D, et al.Epithelial-mesenchymal transition and breast cancer: role, molecular mechanisms and clinical impact[J].Cancer Treat Rev, 2012, 38(6):689-697. [6] Greenburg G,Hay ED.Epithelia suspended in collagen gels can lose polarity and express characteristics of migrating mesenchymal cells [J].J Cell Biol,1982,95:333-339. [7] Wang Y, Yang F, Zhang HX, et al. Cuprous oxide nanoparticles inhibit the growth and metastasis of melanoma by targeting mitochondria[J].Cell Death Dis, 2012, 4(8):3133-3145. [8] Wang Y, Zi XY, Su J, et al.Cuprous oxide nanoparticles selectively induce apoptosis of tumor cells[J].Int J Nanomedicine,2012,7: 2641-2652. [9] Song H, Wang W, Zhao P, et al.Cuprous oxide nanoparticles inhibit angiogenesis via down regulation of VEGFR2 expression[J].Nanoscale,2014,6: 3206-3216. [10] Wen JQ, Cheng ZH, Li QC.Cuprous oxide nanospheres as probes for light scattering imaging analysis of live cells and for conformation identification of proteins[J].Talanta, 2010, 80(3):1400-1405. [11] 王杰军, 应明真.恶性肿瘤的转移机制与治疗策略[J].中国肿瘤生物治疗杂志, 2008, 15(4):305-310. [12] 李爱明, 赵惠民, 揭俊卿.芒柄花黄素对非小细胞肺癌A549细胞增殖及上皮间质转化的抑制作用[J].临床肿瘤学杂志, 2015, 6(6):481-486. [13] 解 昆, 王剑松, 肖民辉,等.MicroRNA-143通过抑制EMT机制延缓膀胱癌演进[J].求医问药(学术版),2012, 2(2):8-10.
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