期刊文献+

肾上腺髓质素对卵巢癌细胞迁移影响及其机制的探讨 被引量:2

Mechanism of migration promotion by adrenomedullin in ovarian cancer cell
原文传递
导出
摘要 目的:观察外源性肾上腺髓质素(AM)对卵巢癌细胞HO8910迁移的影响,并探讨其作用机制。方法:外源性应用AM后,采用划痕实验观察卵巢癌细胞系HO8910的迁移功能,并且利用蛋白质印迹法检测ERK1/2及p-ERK1/2蛋白的表达,以了解AM对ERK1/2蛋白及其活性的影响。结果:外源性给予AM(100nmol/L)的细胞12h迁移率为(62.61±4.51)%,阴性对照细胞的迁移率为(29.23±4.15)%,AM可以促进卵巢癌细胞HO8910的迁移,P=0.001。提前应用ERK1/2抑制剂PD98059的细胞在外源性AM(100nmol/L)的刺激下迁移率为(37.97±3.44)%,比单纯应用AM刺激的细胞迁移率降低,P=0.002。外源性给予AM(100nmol/L)可以促进卵巢癌细胞的ERK1/2蛋白磷酸化。结论:AM促进卵巢癌细胞的迁移,与细胞的ERK1/2活化相关,可能为卵巢癌迁移的治疗提出一个新的研究方向。 OBJECTIVE: To investigate the exogenous adrenomedullin (AM) effection in ovarian cancer cell HO8910 migration and its mechanisms. METHODS: The migration of HO8910 was examined by wound healing test. The expression levels of ERK1/2 and its phosphorylation pattern were examined by western blot. RESULTS: The negative control cells wound healing rate was(29.23士4.15)%. The wound healing rate of cells with exogenous AM (100 nmol/L) was (62.61士4.51)%. AM could promote the motility of HO8910(P=0. 001). Using PD98059,the inhibitor of ERK1/2 one hour before AM,the ceils wound healing rate was(37.97士3.44)% ,so PD98059 could inhibit the AM function in HO8910 (P=0. 002). The phosphorylation of ERK1/2 was significantly increased by AM. CONCLUSION: The AM may play im- portant roles in ovarian epithelial cancer cell migration via phosphorylation of ERK1/2, and may be treated as a new target of ovarian epithelial cancer migration.
出处 《中华肿瘤防治杂志》 CAS 北大核心 2012年第22期1709-1711,共3页 Chinese Journal of Cancer Prevention and Treatment
基金 辽宁省自然科学基金(2009225035)
关键词 卵巢肿瘤 肾上腺髓质素 ERK1/2 迁移 ovarian neoplasms adrenomedullin ERK1/2 migration
  • 相关文献

参考文献4

二级参考文献85

  • 1王树森,管忠震,向燕群,汪波,林桐榆,姜文奇,张力,张惠忠,侯景辉.鼻咽癌组织中EGFR和p-ERK蛋白表达的检测及意义[J].中华肿瘤杂志,2006,28(1):28-31. 被引量:46
  • 2江元,田雪红,袁捷,金月梅,谭育松.肾上腺髓质素在子宫平滑肌肿瘤组织中的表达及其与血管生成和预后的研究[J].中国实用妇科与产科杂志,2006,22(4):262-264. 被引量:1
  • 3陆晓云,张淑兰,鲁艳明,修晓新,孙晓薇.K-Cl协同转运子1在宫颈癌组织中的表达及意义[J].中华医学杂志,2007,87(17):1156-1159. 被引量:3
  • 4Seger R, Krebs E G. The MAPK signaling cascade[J]. FASEB, 1995,9(9):726- 735.
  • 5Cho H S, Chang S H, Chung Y S, et al. Synergistic effect of ERK inhibition on tetrandrine-induced apoptosis in A549 human lung carcinomacells[J]. J Vet Sci,2009,10(1):23- 28.
  • 6ONeill E, Kolch W. Conferring specificity on the ubiquitous Raf/MEK signalling pathway[J]. Br J Cancer,2004, 90(2) :283-288.
  • 7Aplin A E, Stewart S A, Assoian R K, et al. Integrin-mediated adhesion regulates ERK nuclear translocation and phosphorylation of Elk-1[J]. Cell Biol,2001,153(2): 273-281.
  • 8Lee J T Jr, McCubrey J A. The Raf/MEK/ERKsingal transduc tion cascade as a target for chemotherapeutic intervention in leukemia[J]. Leukemia,2002,16(4):486-507.
  • 9Inamoto T, Azuma H, Sakamoto T, et al. Invasive ability of human renal cell carcinoma cell line Caki 2 is accelerated by gamma-aminobutyric acid, via sustained activation of ERK1/2 inducible matrix metalloproteinases[J]. Cancer Invest,2007,25(7):574-583.
  • 10Tsuchihashi K, Takizawa H, Torii T, Ikeda R, Nakahara N, Yuda S, et al. Hypoparathyroidism potentiates cardiovascular complications through disturbed calcium metabolism: possible risk of vitamin D(3) analog administration in dialysis patients with end-stage renal disease. Nephron 2000; 84: 13–20.

共引文献18

同被引文献27

  • 1王天宝,林维浩,石汉平,韩方海,董文广.慢病毒介导CXCR4 RNA干扰对胃癌细胞株SGC7901抑制作用的研究[J].中华肿瘤防治杂志,2013,20(2):102-105. 被引量:2
  • 2王蓓,Marisa Jaconi,BiagioSaittaCoriell,VladimirMarkovCoriell.体外诱导人脐血间充质干细胞未能向心肌细胞转分化[J].中国心血管杂志,2007,12(3):178-181. 被引量:2
  • 3Kitamura K, Kangawa K, Kawamoto M, et al. Adrenomedullim a no- vel hypotensive peptide isolated from human pheoehromoeytoma[J]. Bioehem Biophys Res Commun, 1993, 192(2):553-560.
  • 4Aichler M, Seller C, Tost M, et al. Origin of pancreatic duetal adeno- carcinoma from atypical flat lesions., a comparative study in transgenic mice and human tissues[J]. J Pathol, 2012, 226(5):723-734.
  • 5Baranello C, Mariani M, Andreoli M, et al. Adrenomedullln in ovarian cancer: foe in vitro and friend in vivo? [J/CD]. PLoS, 2012, 7(7) ze40678.
  • 6Keleg S, Kayed H, Jiang X, et al. Adrenomedullin is induced by hypoxia and enhances pancreatic cancer cell invasion [J]. Int J Cancer, 2007, 121(1) :21-32.
  • 7Ramachandran V, Arumugam T, Hwang RF, et al. Adrenomedullin is expressed in pancreatic cancer and stimulates cell proliferation and inva- sion in an autocrine manner via the adrenomedullin receptor, ADMR [J]. Cancer Res, 2007, 67(6) 2666-2675.
  • 8Pang X, Shang H, Deng B, et al. The Interaction of adrenomedullin and macrophages induces ovarian cancer cell migration via activation of rhoA signaling pathway[J]. Int J Mol Sci, 2013, 14(2) :2774-2787.
  • 9Lim SY, Ahn SH, Park H, et al. Transcriptional regulation of ad- renomedullin by oncostatin M in human astroglioma cells: implications for tumor invasion and migrationD. Sei Rep, 2014, 4(1) :6444.
  • 10Permut~-WeyJ, Sellers TA. Epidemiology of ovarian cancer[J]. Methods Mol Biol, 2009, 472:413-437.

引证文献2

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