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miR-152对前列腺癌细胞株迁移和侵袭能力的影响 被引量:2

Effect of miR-152 on migration and invasion of prostate cancer cell lines
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摘要 目的研究miR-152在前列腺癌、前列腺正常组织中的表达情况及其在前列腺癌细胞系中的作用。方法采用TaqMan荧光定量RT-PCR方法检测8例前列腺癌和8例前列腺正常组织的样本中miR-152的表达水平。运用Transwell细胞迁移实验及侵袭实验评估miR-152对前列腺细胞系PC-3和DU145细胞功能的影响。结果与正常前列腺组织相比,miR-152在前列腺癌组织中的表达水平显著下调(P<0.05)。体外实验中上调miR-152的表达可以显著降低前列腺癌细胞的迁移和侵袭能力(P<0.05)。结论 miR-152在前列腺癌中可作为一种肿瘤抑制因子,影响前列腺癌细胞的迁移和侵袭能力。 Objective To investigate the effect of miR-152 on the migration and invation of prostate cancer (PCa) cell lines. Methods The miR-152 expressions in 8 cases of primary PCa and 8 samples of non-malignant prostatic tissue were measured by qRT-PCR. The effects of miR-152 expression on PCa cells were evaluated by Transwell cell migration and invasion assays. Results The miR-152 expression was significantly decreased in primary PCa samples compared with that in non-malignant samples (P〈O. 05). The miR-152 expression significantly reduced the migratory and invasive capabilities of PCa cells in vitro (P〈0.05).Conlclusions Our findings indicate that miR-152 can act as a tumor suppressor and inhibit PCa cell migration and invasion.
出处 《现代泌尿外科杂志》 CAS 2013年第6期546-548,561,共4页 Journal of Modern Urology
基金 国家自然科学基金(No.81171963 81201998)
关键词 前列腺癌 MIR 152 迁移 侵袭 prostate cancer miR-152 migration invasion
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  • 1BARTEL DP. MicroRNAs: genomics? biogenesis, mechanism,and function[J]. Cell,2004,116(2) : 281-297.
  • 2SZCZYRBA J, LOPRICH E, WACH S, et al. The microRNAprofile of prostate carcinoma obtained by deep sequencing [J].Mol Cancer Res?2010,8(4) : 529-538.
  • 3ZHOU X,ZHAO F, WANG ZN,et al. Altered expression ofmiR-152 and miR-148a in ovarian cancer is related to cell prolif-eration[J]. Oncol Rep,2012,27(2) : 447-454.
  • 4TSURUTA T, KOZAKI K, UESUGI A, et al. miR-152 is atumor suppressor microRNA that is silenced by DNA hyperm-ethylation in endometrial cancer[J]. Cancer Res,2011, 71 (20):6450-6462.
  • 5CHEN Y,SONG Y, WANG Z,et al. Altered expression of MiR-148a and MiR-152 in gastrointestinal cancers and its clinical sig-nificance[J]. J Gastrointest Surg,2010,14(7) : 1170-1179.
  • 6LAI EC. MicroRNAs are complementary to 3' UTR sequencemotifs that mediate negative post-transcriptional regulation[J],Nat Genet,2002,30(4): 363-364.
  • 7LIT,LI D, SHA J, et al. MicroRNA-21 directly targetsMARCKS and promotes apoptosis resistance and invasion inprostate cancer cells[J], Biochem Biophys Res Commun,2009?383(3): 280-285.
  • 8KONG D,LI Y, WANG Z, et al. miR-200 regulates PDGF-D-mediated epithelial-mesenchymal transition, adhesion, and inva-sion of prostate cancer cells[J]. Stem Cells,2009*27(8) : 1712-1721.
  • 9LIU C,KELNAR K,LIU B,et al. The microRNA miR-34a in-hibits prostate cancer stem cells and metastasis by directly re-pressing CD44[J]. Nat Med,2011,17(2)211-215.
  • 10SPAHN M,KNEITZ S, SCHOLZ CJ,et al. Expression of mi-croRNA-221 is progressively reduced in aggressive prostate canc-er and metastasis and predicts clinical recurrence[J]. Int J Canc-er,2010,127(2) : 394-403.

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