期刊文献+

蛇床子素对骨肉瘤细胞增殖、迁移和侵袭的抑制作用及其机制 被引量:3

The Inhibitory Efficacy of Osthole on the Proliferation,Migration and Invasion of Osteosarcoma Cells and Its Mechanisms
原文传递
导出
摘要 目的:探讨蛇床子素(Osthole,OST)对人骨肉瘤细胞U2-OS增殖、迁移、侵袭的抑制作用及其机制。方法:培养人骨肉瘤细胞U2-OS,采用不同浓度的OST处理细胞,四甲基偶氮唑盐(MTT)法检测细胞增殖情况,克隆形成实验检测细胞克隆形成的能力,细胞划痕实验观察细胞迁移能力,Transwell小室法检测细胞侵袭作用,Western-Blot法检测PTEN、pAKT、AKT蛋白的表达。结果:MTT法结果表明OST能够抑制人骨肉瘤细胞U2-OS的增殖并呈剂量依赖性;克隆形成实验结果表明OST能够抑制U2-OS细胞的克隆形成能力;细胞划痕实验和细胞侵袭实验结果显示OST处理后细胞的迁移和侵袭能力明显降低;Western-Blot结果显示OST处理后PTEN蛋白的表达明显增加,pAKT蛋白的表达明显下降,并呈现一定的剂量依赖性。结论:OST可抑制人骨肉瘤细胞U2-OS增殖、迁移、侵袭,其可能的作用机制与调控PTEN-AKT信号通路有关。 Objective:To explore the inhibitory efficacy of osthole(OST)on the proliferation,migration and invasion of human osteosarcoma U-2 OS cells and its mechanisms.Methods:U2-OS were cultured and treated with the different doses of OST.The efficacy of OST on cell proliferation was detected by MTT assay.The efficacy of OST on cell colony formation was detected by colony formation assay.The efficacy of OST on cell migration was tested by wound healing assay.The efficacy of OST on cell invasion was detected by Transwell invasion assay.The efficacy of OST on the expression of PTEN,pAKT and AKT proteins was assessed by Western-Blot assay.Results:MTT assay showed that OST could inhibit the proliferation of U2-OS cells in a dose-dependent manner.The colony formation assay showed that OST could significantly inhibit the colony formation capacity of U2-OS cells.The wound healing and Transwell invasion assays showed that OST could greatly decreased the cell migration and invasion of osteosarcoma cells.The Western-Blot assay showed that OST could significantly increase the expression of PTEN,and decreased the expression of pAKT protein in a dose-dependent manner.Conclusion:OST could inhibit the proliferation,migration and invasion of human osteosarcoma U2-OS cells,which may be associated with the regulation of PTEN-AKT signaling.
作者 姜习凤 李光飞 曹国文 JIANG Xifeng;LI Guangfei;CAO Guowen(Department of Orthopaedics,The Second Affiliated Hospital of Soochow University,Suzhou 215004,Jiangsu China;Department of Pharmacy,The Second Affiliated Hospital of Soochow University,Suzhou 215004,Jiangsu China)
出处 《中国中医骨伤科杂志》 CAS 2021年第5期12-15,20,共5页 Chinese Journal of Traditional Medical Traumatology & Orthopedics
关键词 蛇床子素 骨肉瘤 细胞侵袭 磷酸酶和紧张素同源基因 osthole osteosarcoma cell invasion phosphatase and tensin homolog
  • 相关文献

参考文献3

二级参考文献17

  • 1Rad MP,Fattahi Masoum SH,Rad MS,et al.Primary Osteosarcoma of the Sternum:A case Report and Review of the Literature[J].Arch Bone Jt Surg,2014,2(4):272-275.
  • 2Billiet T,Rutgeerts P,Vermeire S,et al.Targeting TNF -α for the treatment of inflammatory bowel disease [J].Expert Opin Biol Ther,2014,14(1):75-101.
  • 3Wen YC,Lee WJ,Chien MH,et al.By inhibiting snail signaling and miR -23a -3p,osthole suppresses the EMT-mediated metastatic ability in prostate cancer[J].Oncotarget,2015,6(25):21120-21136.
  • 4Lin YC,Lin JC,Way TD,et al.Osthole inhibits insulin-like growth factor-1-induced epithelial to mesenchymal transition via the inhibition of PI3K/Akt signaling pathway in human brain cancer cells [J].J Agric Food Chem,2014,62(22):5061-5071.
  • 5Gao Z,Wen Q,Zou S.Osthole augments therapeutic efficiency of neural stem cells-based therapy in experimental autoimmune encephalomyelitis [J].J Pharmacol Sci,2014,124(1):54-65.
  • 6Xie L,Jiang F,Zhang XK,et al.Honokiol sensitizes breast cancer cells to TNF-α induction of apoptosis by inhibiting Nur77 expression[J].Br J Pharmacol,2016,173(2):344-356.
  • 7Mahul-Mellier AL,Pazarentzos E,Lin B et al.Deubiquitin-ating protease USP2a targets RIP1 and TRAF2 to mediate cell death by TNF[J].Cell Death Differ,2012,19(5):891-899.
  • 8Vanlangenakker N,Vanden Berghe T,Zobel K et al.cIAPl and TAKl protect cells from TNF -induced necrosis by preventing RIP1/RIP3-dependent reactive oxygen species production[J].Cell Death Differ,2011,18(4):656_665.
  • 9Ding Z,Liu Y,Shen A,et al.Spyl induces de-ubiquitinating of RIP1 arrest and confers glioblastoma's resistance to tumor necrosis factor (TNF-α)-induced apoptosis through suppressing the association of CLIPR-59 and CYLD [J].Cell Cycle,2015,14(13):2149-2159.
  • 10吴琴,高云.氧化苦参碱药理作用的分子机制研究进展[J].中国药理学通报,2015,31(6):759-762. 被引量:53

共引文献12

同被引文献90

引证文献3

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部