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微小RNA-100靶向成纤维生长因子受体调控胰腺癌细胞的增殖 被引量:1

miR-100 regulates cell growth through targeting FGFR3 in patients with pancreatic cancer
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摘要 目的 探讨微小RNA(miR)-100对成纤维生长因子受体3(FGFR3)调控及其对胰腺癌细胞增殖的影响.方法 采用实时PCR检测17对胰腺癌和癌旁组织中miR-100的表达水平.应用CCK-8试剂盒检测过表达miR-100对胰腺癌细胞株增殖的影响.利用分子生物学技术构建FGFR3的野生型及突变型3’-UTR报告基因,分析miR-100对FGFR3的调控作用,然后采用实时PCR和蛋白印迹检测过表达miR-100对FGFR3 mRNA和蛋白表达水平的影响.应用CCK-8、5-溴脱氧尿嘧啶核苷(Edu)探讨特异性敲低FGFR3对胰腺癌细胞株增殖的影响.结果 miR-100在胰腺癌组织中呈低表达水平(P<0.05).过表达miR-100可显著抑制胰腺癌细胞的增殖(P<0.05).报告基因分析显示miR-100能够显著下调FGFR3的野生型3’-UTR报告基因的荧光表达(P<0.05),而对突变型报告基因和空白对照组的荧光表达影响不大.实时PCR和蛋白印迹检测显示miR-100可显著抑制FGFR3的mRNA和蛋白表达(P<0.05).特异性敲低FGFR3后明显抑制胰腺癌细胞的增殖(P<0.05).结论 miR-100可通过调控FGFR3表达来抑制胰腺癌细胞的增殖,从而在胰腺癌中发挥抑癌基因的功能. Objective To investigate the effects of miR-100 on the proliferation of MIA PaCa-2 and CFPAC-1 cells through targeting fibroblast growth factor receptor 3 (FGFR3).Methods miR-100 expression levels in 17 cancer tissues and 17 nonmalignant tissues were examined by Real-time PCR.The effect of miR-100 overexpression on cell proliferation was examined by CCK-8 assay in vitro.Luciferase assay was used to confirm that miR-100 could directly target FGFR3.Real-time PCR and Western blot were used to examine the expression of FGFR3 in miR-100 overexpressing pancreatic cancer cells.The predicted target gene of miR-100,FGFR3,was downregulated by siRNA,and its effect on cell proliferation was also examined.Cell proliferation was analyzed using CCK-8 and Edu assay.Results miR-100 was lowly expressed in pancreatic cancer tissues (P 〈 0.05).In pancreatic cancer cells,the transfection of lv-miR-100 was able to upregulate the endogenous expression of miR-100 and inhibit the cell proliferation (P 〈0.05).Luciferase assay showed FGFR3 was the direct target of miR-1O0.FGFR3 was significantly downregulated by overexpressing miR-100 in pancreatic cancer cells (P 〈0.05),and FGFR3 knockdown by specific siRNA exerted the similar effect as miR-100 overexpression (P 〈 0.05).Conclusions Our study identified a new miRNA regulator,miR-100,and clarified a novel mechanism of how miR-100 regulates cell proliferation in pancreatic cancer.The strategy of overexpressing the tumor suppressor miR-100 may provide a new therapeutic approach for treating patients with pancreatic cancer.
机构地区 贵州医科大学
出处 《中华肝胆外科杂志》 CAS CSCD 北大核心 2016年第2期116-120,共5页 Chinese Journal of Hepatobiliary Surgery
关键词 胰腺癌 微小RNA-100 成纤维生长因子受体3 细胞增殖 Pancreatic cancer microRNA-100 Fibroblast growth factor receptor 3 Cell proliferation
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  • 1Rosenberg L. Treatment of pancreatic cancer: promises and prob- lems of tamoxifen, somatostatin analogs, and gemcitabine[J]. Int J Pancreatol, 1997,22(2) :81-93. 被引量:1
  • 2Siegel R, Ma J, Zou Z, et al. Cancer statistics, 2014[J]. CA Cancer J Clin, 2014,64( 1 ) :9-29. 被引量:1
  • 3Michl P, Gress TM. Current concepts and novel targets in ad- vanced pancreatic cancer[ J ]. Gut, 2013,62 ( 2 ) :317-326. 被引量:1
  • 4Fang X, Thornton C, Scheffler BE, et al. BenzoN3 pyrene decrea- ses global and gene specific DNA methylation during zebrafish de- velopment[ J]. Environ Toxicol Pharmacol, 2013,36( 1 ) :40-50. 被引量:1
  • 5Wohlhueter RM, Mcivor RS, Plagemann PG. Facilitated transporl of uracil and 5-fluorouracil, and permeation of omtic acid into cul- tured mammalian cells [ J ]. J Cell Physiol, 1980, 104 (3) : 309 -319. 被引量:1
  • 6Lmgley DB, Harkin DP, Johnston PG. 5-flunrouracil: mecha- nisms of action and clinical strategies[ J]. Nat Rev Cancer, 2003, 3 (5) :330-338. 被引量:1
  • 7lshida S, Lee J, Thiele DJ, et al. Uptake of the anticancer drug cisplatin mediated by the copper transporter Ctrl in yeast and mammals [ J ]. Proc Natl Acad Sci USA, 2002, 99 ( 22 ) : 14298-14302. 被引量:1
  • 8Ummat A, Rechkoblit O, Jain R, el al. Stnlctural basis fir cispla- tin DNA damage tolerance by human polymcrase eta during cancer chemotherapy [ J ]- Nat Struct Mol Biol, 2012,19 ( 6 ) :628-632. 被引量:1
  • 9Kelland 1,. The resurgence of platinum-based cancer chemotherapy [J]. Nat Rev Cancer, 2007,7(8) :573-584. 被引量:1
  • 10Morgan MA, Parsels LA, Maybaum J, et al. hnproving gcmcit- abine-mediated radionsitization using molecularly targeted Ihera- or, a review[ J]. Clin Cancer Res, 2008,14(21 ) :6744-6750. 被引量:1

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