期刊文献+

PI-103对人黑色素瘤A375细胞迁移和侵袭能力的影响及其机制研究

Effects of PI-103 on migratory and invasive abilities of human melanoma A375 cells and its mechanism
下载PDF
导出
摘要 目的观察PI-103在体外对人黑色素瘤A375细胞迁移和侵袭能力的影响,并探讨可能的作用机制。方法应用MTT法检测不同浓度PI-103对A375细胞增殖的影响,Transwell小室实验检测0.1、0.2μmol/L PI-103对A375细胞迁移能力和侵袭能力的影响,Western Blot法测定细胞基质金属蛋白酶(MMP)-2、MMP-9的表达。结果 0.1、0.2μmol/L PI-103对A375细胞增殖的抑制作用不明显(P>0.05);在浓度高于0.4μmol/L时,PI-103能够明显抑制A375细胞的增殖(P<0.05)。0.1μmol/L PI-103作用后,迁移实验和运动实验穿膜细胞数分别为(91.73±13.80)、(63.67±8.54),与对照组比较明显减少,差异有统计学意义(P<0.05);0.2μmol/L PI-103作用后,迁移实验和运动实验穿膜细胞数分别为(64.07±9.22)、(34.80±7.89),与对照组比较明显减少,差异有统计学意义(P<0.05)。0.1、0.2μmol/L PI-103作用后,A375细胞MMP-2、MMP-9蛋白表达明显低于对照组,差异有统计学意义(P<0.05)。结论 PI-103可通过下调MMP-2、MMP-9的表达抑制A375细胞迁移和侵袭,为其应用于抗恶性黑素瘤转移治疗提供了实验依据。 Objective To investigate the effects of PI-103 on the migratory and invasive abilities of human melanoma A375 cells in vitro and its mechanism. Methods The effects of PI-103 with different concentration on the proliferation of A375 cells were detected by MTT assay. The effects of PI-103 at 0.1, 0.2 μmol/L concentration on the migratory and invasive abilities of A375 cells were detected by transwell chamber assay. The expressions of MMP-2 and MMP-9 in A375 cells were determined by Western Blot. Results The inhibition effects on the proliferation of A375 cells treat-ed with PI-103 at 0.1, 0.2μmol/L concentration were not significant (P〉0.05). The proliferation of A375 cells treated with PI-103 at the concentration higher than 0.4μmol/L was significantly inhibited (P〈0.05). The numbers of trans-membrane cells in the migration and invasion experiment treated with PI-103 at 0.1 μmol/L concentration were (91.73±13.80), (63.67±8.54) respectively, which were significantly decreased compared with control group (P〈 0.05). The numbers of transmembrane cells in the migration and invasion experiment treated with PI-103 at 0.2 μmol/L con-centration were (64.07±9.22), (34.80±7.89) respectively, which were significantly decreased compared with control group (P〈 0.05). The expressions of MMP-2 and MMP-9 in A375 cells treated with PI-103 at 0.1, 0.2 μmol/L con-centration were significantly decreased compared with control group (P〈 0.05). Conclusion PI-103 can inhibit the mi-gration and invasion of A375 cells by down-regulation of the expressions of MMP-2 and MMP-9, which provide the experimental basis for the prevention of melanoma metastasis.
出处 《中国医药导报》 CAS 2014年第25期14-17,共4页 China Medical Herald
基金 四川省卫生厅立项科研课题(编号110466)
关键词 PI-103 黑色素瘤 迁移 侵袭 PI-103 Melanoma Migration Invasion
  • 相关文献

参考文献18

  • 1陆茂,叶俊儒,樊元春,唐樱,黄蓉飞.磷酸化mTOR在恶性黑素瘤中的表达及与CyclinD1的关系[J].四川医学,2010,31(2):163-165. 被引量:3
  • 2Uzdensky AB,Demyanenko SV,Bibov MY. Signal transdue- tion in human cutaneous melanoma and target drugs [J].C urr Cancer Drug Targets, 2013,13 (8) : 843-866. 被引量:1
  • 3Lopez-Fauqued M,Gil R,Grueso J,et al. The dual PI3K/ mTOR inhibitor PI-103 promotes immunosuppression, in vivo tumor growth and increases survival of so rafenib- treated melanoma cells [J]. Int J Cancer,2010,126(7): 1549-1561. 被引量:1
  • 4Wu P, Hu YZ. PI3K/Akt/mTOR pathway inhibitors in can- cer: a perspective on clinical progress [J]. Curr Med Chem, 2010,17(35) :4326-4321. 被引量:1
  • 5Mazzoletti M,Bortolin F, Brunelli L, et al. Combination of PI3K/mTOR inhibitors: antitumor activity and molecular correlates [J]. Cancer Res, 2011,71 ( 13 ) : 4573-4584. 被引量:1
  • 6刘俊,蔡云朗,任慕兰,吴迪,曾娅.PI-103对人卵巢癌细胞株SKOV3/DDP顺铂化疗效果的影响[J].东南大学学报(医学版),2013,32(5):574-579. 被引量:6
  • 7Saturno G,Valenti M,De Haven Brandon A,et al. Com- bining trail with PI3 kinase or HSP90 inhibitors enhances apoptosis in colorectal cancer ceils via suppression of sur- vival signaling [J]. Oncotarget, 2013,4 (8) : 1185-1198. 被引量:1
  • 8Yi YW,Hong W,Kang HJ,et al. Inhibition of the PI3K/ AKT pathway potentiates cyt0toxieity of EGFR kinase in- hibitors in triple-negative breast eaneer cells [J]. J Cell Mol Med,2013,17(5) :648-656. 被引量:1
  • 9Santo EE,Stroeken P,Sluis PV,et al. FOXO3a is a major target of inactivation by PI3K/AKT signaling in aggressive neuroblastoma [J]. Cancer Res,2013,73(7) :2189-2198. 被引量:1
  • 10李娜,祝聪聪,肖永红,张文丽,刘亦民.PI3K抑制剂对四氯化碳刺激的肝星状细胞增殖和Ⅰ型胶原表达的影响[J].西安交通大学学报(医学版),2013,34(2):164-167. 被引量:12

二级参考文献35

  • 1司徒杰,高新,湛海伦,温星桥,邱剑光.CIK细胞免疫疗法在肾癌治疗中的应用[J].白求恩军医学院学报,2005,3(4):215-216. 被引量:9
  • 2Yang Cheng,Jian Ping,Huai-Dong Xu,Hai-Jun Fu,Zhao-Hui Zhou.Synergistic effect of a novel oxymatrine-baicalin combination against hepatitis B virus replication, a smooth muscle actin expression and typeⅠcollagen synthesis in vitro[J].World Journal of Gastroenterology,2006,12(32):5153-5159. 被引量:33
  • 3Chiang GG, Abraham RT. Targeting the mTOR signaling network in cancer[ J ]. Trends Mol Med ,2007,13 (10) :433 - 442. 被引量:1
  • 4Ramirez JA,Guitart J,Rao MS,et al. Cyclin DI expression in melanocytic lesions of the skin [ J ]. Ann Diagn Pathol, 2005,9 ( 4 ) : 185 - 188. 被引量:1
  • 5Robertson GP. Functional and therapeutic significance of Akt deregulation in malignant melanoma [ J ]. Cancer Metastasis, 2005,24 (2) : 273 - 285. 被引量:1
  • 6Alexia C, Bras M, Fallot G, et al. Pleiotropie effects of PI-3' kinase/ Akt signaling in human hepatoma cell proliferation and drug-induced apoptosis[ J]. Ann N Y Acad Sci ,2006,1090(12) : 1 - 17. 被引量:1
  • 7Shinohara M, Chung YJ, Saji M ,et al. Akt in thyroid tumorgenesis and progression [ J ]. Endocrinology, 2007,148 ( 3 ) :942 - 947. 被引量:1
  • 8Karbowniczek M, Spittle CS, Morrison T, et al. mTOR is activated in the majority of malignant melanomas[ J]. J Invest Dermatol,2008,128 (4) :980-987. 被引量:1
  • 9Averous J, Fonseca BD, Proud CG. Regulation of CyclinD1 expression by mTORC1 signaling requires eukaryotic initiation factor 4E-binding protein 1 [J]. Oncogene,2008,27(8) :1106 - 1113. 被引量:1
  • 10Gao N, Zhang Z ,Jiang BH, et al. GI cell cycle progression and the expression of G1 cyclins are regulated by PBK/AKT/mTOR/p70S6K1 signaling in human ovarian cancer cells[ J]. Am J Physiol Cel Physiol,2004,287 (2) :281 - 291. 被引量:1

共引文献18

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