期刊文献+

miR-30c对胃癌细胞株HGC-27侵袭转移能力的影响

Effects of miR-30c on the invasion and metastasis of HGC-27 cells in vitro
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摘要 目的探讨miR-30c对胃癌细胞株HGC-27侵袭转移能力的影响。方法使用miR-30c mimics和inhibitor分别进行miR-30c的过表达和抑制,采用划痕实验和transwell小室实验分析癌细胞迁移和侵袭能力,Western blot检测上皮间质转化(EMT)相关蛋白E-cadherin、Vimentin和Fibronectin的表达差异。结果抑制miR-30c可促进胃癌细胞系HGC-27的侵袭(P<0.05),同时高表达miR-30c可抑制细胞侵袭(P<0.05)。抑制miR-30c后E-cadherin表达降低、Vimentin和Fibronectin表达升高,高表达miR-30c后E-cadherin的表达升高、Vimentin和Fibronectin表达下降。结论 miR-30c可能通过调节上皮间质转化(EMT)相关蛋白来影响胃癌的侵袭能力。 Objective To explore the effect of miR-30c on the invasion and metastasis of human gastric cancer cell line HGC-27 in vitro. Methods The overexpression and inhibition of miR-30c were induced with miR-30c mimics and miR-30c inhibitor. Wound healing assay and transwell invasion assay were conducted to assess the effects of migration and invasion capabilities of HGC-27 cells. The expression of epithelial mesenchymal transition (EMT) related proteins (E-cadherin, vimentin and fibronectin) was determined by Western blot. Results The inhibition of miR-30c promoted the migration and invasion capabilities of HGC-27 cells ( P 〈 0.05 ). Meanwhile, the overexpression of miR-30c inhibited the migration and invasion capabilities of HGC-27 cells (P 〈 0.05 ). The inhibition of miR-30c decreased the levels of E-cadherin expression and increased the levels of vimentin and fibronectin expression. The overexpression of miR-30c increased the levels of E-cadherin expression and decreased the levels of vimentin and fibronectin expression. Conclusion The results suggest that miR-30c may influence the invasion and metastasis capabilities of human gastric cancer via regulating EMT related proteins.
出处 《山西医科大学学报》 CAS 2015年第1期9-12,共4页 Journal of Shanxi Medical University
关键词 miR-30c 上皮间质转化 侵袭 胃癌 miR-30c epithelial mesenchymal transition metastasis gastric cancer
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参考文献14

  • 1李诚,周健,裘炯良.胃癌流行病学与分子生物学病因的研究进展[J].肿瘤防治研究,2004,31(2):115-118. 被引量:33
  • 2俞秀冲,宋皓军,郭俊明.MiRNA影响胃癌转移的机制[J].中国生物化学与分子生物学报,2011,27(10):907-913. 被引量:8
  • 3张婷,崔戈,邵圣文,叶家辉,黄斌,潘臻.调控肿瘤上皮–间质转化及肿瘤干细胞样特性的信号通路串话[J].中国细胞生物学学报,2012,34(11):1147-1155. 被引量:4
  • 4张慧君,朱军,刘鸿程,王和勇,陈晓峰.上皮间质转化在肿瘤侵袭转移中的研究进展[J].生命科学,2009,21(4):556-559. 被引量:7
  • 5Lewis BP,Bui^e CB,Bartel DP. Conserved seed pairing,often flankedby adenosines,indicates that thousands of human genes are microH-NA targets[J].Cell,2005,120(1) ;15-20.
  • 6Li X,Zhang Y,Zhang H,et al. miRNA-223 promotes gastric cancerinvasion and metastasis by targeting tumor suppressor EPB41L3[J].Mol Cancer Res,2011,9(7) :824-833.
  • 7Tie J,Pan Y,Zhao L,et al. MiR-218 inhibits invasion and metas-tasis of gastric cancer by targeting the Robol receptor [ J ]. PLoSGenetics,2010,6(3) :el000879.
  • 8Ueda T,Volinia S, Okumura H,ei al. Relation between microR-NA expression and progression and prognosis of gastric cancer: amicroRNA expression analysis [ J ]. Lancet Oncol ,2010,11 (2):136 -146.
  • 9Zhou H,Xu X,Xun Q,et al. microRNA-30c negatively regulatesendometrial cancer cells by targeting metastasis-associated gene-1[J]. Oncol Reports,2012,27(3) :807 -812.
  • 10Bockhom J, Yee K, Chang YF, et al. MicroRNA-30c targets cy-toskeleton genes involved in breast cancer cell invasion [ J ]. BreastCancer Res Treat,2013 ,137(2) :373 -382.

二级参考文献62

  • 1Zhu, Yi-Min,Zhong, Zheng-Xiang,Liu, Zhi-Ming.Relationship between let-7a and gastric mucosa cancerization and its significance[J].World Journal of Gastroenterology,2010,16(26):3325-3329. 被引量:17
  • 2Hong-He Zhang,Xian-Jun Wang,Guo-Xiong Li,En Yang,Ning-Min Yang.Detection of let-7a microRNA by real-time PCR in gastric carcinoma[J].World Journal of Gastroenterology,2007,13(20):2883-2888. 被引量:48
  • 3Greenburg G, Hay ED. Epithelia suspended in collagen gels can lose polarity and express characteristics of migrating mesenchymal cells. J Cell Biol, 1982, 95(1): 333-9.
  • 4Lee MY, Chou CY, Tang MJ, et al. Epithelial-mesenchymal transition in cervical cancer: correlation with tumor progression, epidermal growth factor receptor overexpression and snail up-regulation. Clin Cancer Res, 2008, 14(15): 4743-50.
  • 5Thuault S, Valcourt U, Petersen M, et al. Transforming growth factor-β employs HMGA2 to elicit epithelial-mesenchymal transition. J Cell Biol, 2006, 174(2): 175-83.
  • 6Thuault S, Tan EJ, Peinado H, et al. HMGA2 and Smads coregulate SNAIL1 expression during induction of epitheliai-to-mesenchymal transition. J Biol Chem, 2008, 283(48): 33437-46.
  • 7Kong WL, Yang H, He LL, et al. MicroRNA-155 is regulated by the transforming growth factor -β/Smad pathway and contributes to epithelial cell plasticity by targeting RhoA. Mol Cell Biol, 2008, 28(22): 6773-84.
  • 8Liu X. Inflammatory cytokines augments TGF-β1-induced epithelial-mesenchymal transition in A549 cells by up-regulating TβR-I. Cell Motil Cytoskeleton, 2008, 65(12): 935-44.
  • 9Roberts AB, Wakeield LM. The two faces of transforming growth factor-β in carcinogenesis. Proc Natl Acad Sci USA, 2003, 100(15): 8621-3.
  • 10Graham TR, Zhan HE, Odero-Marah VA, et al. Insulin-like growth factor-Ⅰ-dependent up-regulation of ZEB1 drives epithelial-to-mesenchymal transition in human prostate cancer. Cancer Res, 2008, 68(7): 2479-88.

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