期刊文献+

miR-19a-3p通过PTEN调节人胃癌细胞增殖水平 被引量:2

miR-19a-3p regulates the proliferation of gastric cancer cells via targeting PTEN
下载PDF
导出
摘要 目的探讨miR-19a-3p通过下游靶基因PTEN调节人胃癌MKN28细胞增殖水平,从microRNA角度阐明胃癌细胞增殖的机制,为胃癌的防治提供新的思路。方法收集20例人胃癌组织和癌旁组织,实时荧光定量PCR方法分析miR-19a-3p表达水平;在人胃癌MKN28细胞中转染miR-19a-3p类似物和miR-19a-3p反义链,用实时荧光定量PCR方法分析miR-19a-3p表达水平,用MTT法检测细胞增殖水平;在人胃癌MKN28细胞中转染miR-19a-3p类似物和miR-19a-3p反义链,用Western blot方法分析PTEN蛋白水平;在人胃癌MKN28细胞中共转染miR-19a-3p反义链和PTEN特异性的小RNA片段(siRNA-PTEN,si-PTEN),用Western blot方法分析PTEN蛋白水平,用MTT法检测细胞增殖水平。结果胃癌组织中miR-19a-3p表达水平明显高于癌旁组织(P<0.05)。转染miR-19a-3p类似物组MKN28细胞中miR-19a-3p水平和细胞增殖水平均明显高于阴性对照组(P<0.05),转染miR-19a-3p反义链组MKN28细胞中miR-19a-3p水平和细胞增殖水平均明显低于反义阴性对照组(P<0.05)。转染miR-19a-3p类似物组与阴性对照组PTEN mRNA水平差异无统计学意义(P>0.05),miR-19a-3p反义链组与反义阴性对照组PTEN mRNA水平差异无统计学意义(P>0.05)。miR-19a-3p反义链组MKN28细胞增殖水平低于反义阴性对照组,PTEN siRNA组MKN28细胞增殖水平高于反义阴性对照组,miR-19a-3p反义链+PTEN siRNAMKN28细胞增殖水平低于PTEN siRNA组(P<0.05)。结论在人胃癌MKN28细胞中miR-19a-3p通过调节下游靶基因PTEN影响细胞增殖。 Objective To discuss the effect of miR-19a-3p on the proliferation of human gastric cancer cell via targeting PTEN,which provided new ideas for the prevention and treatment of gastric cancer.Methods Gastric carcinoma tissue specimens and matched adjacent tissues were obtained from twenty patients who were identified as aggressive gastric adenocarcinoma.Real-time PCR was used to analyze the levels of miR-19a-3p in gastric carcinoma tissue specimens and matched adjacent tissues.miR-19a-3p mimic and miR-19a-3p inhibitor were transfected into MKN28 cells.Real-time PCR was used to analyze the level of miR-19a-3p.And MTT assay was used to determine the proliferation of MKN28 cell.miR-19a-3p mimic and miR-19a-3p inhibitor were transfected into MKN28 cells.Western blot was used to measure the protein level of PTEN.miR-19a-3p inhibitor and siRNA-PTEN were transfected into MKN28 cells.Western blot was used to measure the protein level of PTEN.And MTT assay was used to determine the proliferation of MKN28 cell.Results Compared with adjacent tissues,miR-19a-3p expression was increased in gastric cancer tissues(P<0.05).Compared with negative mimic control group,transfection with miR-19a-3p mimic increased miR-19a-3p expression(P<0.05).Compared with negative inhibitor control group,transfection with miR-19a-3p inhibitor decreased miR-19a-3p expression(P<0.05).The level of PTEN mRNA did not significantly change in MKN28 cells transfected with miR-19a-3p mimic(P>0.05)or miR-19a-3p inhibitor(P>0.05).The proliferation of MKN28 cells was inhibited in MKN28 cells transfected with miR-19a-3p inhibitor(P<0.05)and was promoted in MKN28 cells transfected with si-PTEN(P<0.05).Compared with si-PTEN group,the proliferation of MKN28 cells was decreased in MKN28 cells co-transfected with si-PTEN and miR-19a-3p inhibitor(P<0.05).Conclusion miR-19a-3p regulated the proliferation of human gastric cancer cells via targeting PTEN.
作者 聂红峰 张萍 贺雪霞 曹青 侯艳青 孟磊 NIE Hong-feng;ZHANG Ping;HE Xue-xia;CAO Qing;HOU Yan-qing;MENG Lei(The Third Department of Abdominal Surgery,the First Hospital of Xingtai,Hebei Province,Xingtai 054001,China;Department of Respiratory Medicine,the People's Hospital of Xingtai,Hebei Province,Xingtai 054001,China)
出处 《河北医科大学学报》 CAS 2019年第5期538-542,546,共6页 Journal of Hebei Medical University
关键词 胃肿瘤 微RNAS 细胞增殖 stomach neoplasms microRNAS cell proliferation
  • 相关文献

参考文献2

二级参考文献32

  • 1戴丹,徐燕丽.MicroRNA与恶性淋巴瘤相关性研究进展[J].河北医科大学学报,2009,30(10):1106-1108. 被引量:2
  • 2Cheng LL, Itahana Y, Lei ZD, Chia NY, Wu Y, Yu Y, ZhangSL, Thike AA, Pandey A, Rozen S, Voorhoeve PM, Yu Q, TanPH, Bay BH, Itahana K, Tan P. TP53 genomic status regulatessensitivity of gastric cancer cells to the histone methylationinhibitor 3-deazaneplanocin A (DZNep). Clin Cancer Res 2012;18: 4201-4212 [PMID: 22675170 DOI: 10.1158/1078-0432.CCR-12-0036].
  • 3Buffart TE, Carvalho B, van Grieken NC, van Wieringen WN,Tijssen M, Kranenbarg EM, Verheul HM, Grabsch HI, Ylstra B,van de Velde CJ, Meijer GA. Losses of chromosome 5q and 14qare associated with favorable clinical outcome of patients withgastric cancer. Oncologist 2012; 17: 653-662 [PMID: 22531355DOI: 10.1634/theoncologist.2010-0379].
  • 4Xia JT, Chen LZ, Jian WH, Wang KB, Yang YZ, He WL, HeYL, Chen D, Li W. MicroRNA-362 induces cell proliferationand apoptosis resistance in gastric cancer by activation of NF-κB signaling. J Transl Med 2014; 12: 33 [PMID: 24495516 DOI:10.1186/1479-5876-12-33].
  • 5Cao W, Yang W, Fan R, Li H, Jiang J, Geng M, Jin Y, Wu Y.miR-34a regulates cisplatin-induce gastric cancer cell death bymodulating PI3K/AKT/survivin pathway. Tumour Biol 2014; 35:1287-1295 [PMID: 24068565 DOI: 10.1007/s13277-013-1171-7].
  • 6Calin GA, Croce CM. MicroRNA signatures in human cancers.Nat Rev Cancer 2006; 6: 857-866 [PMID: 17060945 DOI:10.1038/nrc1997].
  • 7Wu Q, Yang Z, An Y, Hu H, Yin J, Zhang P, Nie Y, Wu K, Shi Y,Fan D. MiR-19a/b modulate the metastasis of gastric cancer cellsby targeting the tumour suppressor MXD1. Cell Death Dis 2014; 5:e1144 [PMID: 24675462 DOI: 10.1038/cddis.2014.110].
  • 8Pan HW, Li SC, Tsai KW. MicroRNA dysregulation in gastriccancer. Curr Pharm Des 2013; 19: 1273-1284 [PMID: 23092346DOI: 10.2174/138161213804805621].
  • 9Ueda T, Volinia S, Okumura H, Shimizu M, Taccioli C, RossiS, Alder H, Liu CG, Oue N, Yasui W, Yoshida K, Sasaki H,Nomura S, Seto Y, Kaminishi M, Calin GA, Croce CM. Relationbetween microRNA expression and progression and prognosisof gastric cancer: a microRNA expression analysis. LancetOncol 2010; 11: 136-146 [PMID: 20022810 DOI: 10.1016/S1470-2045(09)70343-2].
  • 10Wang F, Sun GP, Zou YF, Hao JQ, Zhong F, Ren WJ. MicroRNAsas promising biomarkers for gastric cancer. Cancer Biomark 2012;11: 259-267 [PMID: 23248184 DOI: 10.3233/CBM-2012-00284].

共引文献17

同被引文献16

引证文献2

二级引证文献1

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