期刊文献+

甲状腺乳头状癌中miR-155、SOCS1的表达及临床意义 被引量:6

Expression and clinical significance of mir-155 and SOCS1 in thyroid papillary carcinoma
原文传递
导出
摘要 目的探讨甲状腺乳头状癌(PTC)组织中miR-155及SOCS1基因的表达情况,分析两者表达与PTC临床病理的相关性。方法在60例PTC组织、20例正常甲状腺组织中采用实时荧光定量RT-PCR法分别检查miR-155、SOCS1基因mRNA的表达水平;分析PTC与正常甲状腺组织中miR-155、SOCS1的表达差异及其与PTC临床病理的相关性。结果 PTC中miR-155表达量高于正常甲状腺组织,而PTC中SOCS1基因表达量低于正常甲状腺组织,两者差异均有统计学意义(P<0.05);PTC中miR-155、SOCS1基因的表达水平与肿瘤TNM分期、病理分级及淋巴结转移均相关(P<0.05),而与年龄、性别及肿瘤大小等因素无关(P>0.05)。在PTC中miR-155、SOCS1基因的表达呈负相关(r=-0.564,P<0.05)。结论 PTC中miR-155、SOCS1基因表达异常,提示miR-155的表达上调可能通过调控SOCS1的表达参与了PTC发生发展,miR-155、SOCS1基因两者有可能成为PTC治疗新的靶点。 Objective To investigate the expression of miR-155 and suppressor of cytokine signaling-1(SOCS1)in thyroid papillary carcinoma(PTC),and to analyze the correlation between the two expressions of PTC with clinic pathology.Methods The expressions of miR-155 and SOCS1 mRNA were examined by real-time fluorescence quantitative RT-PCR method in 60 cases of PTC tissues and 20 cases of normal thyroid tissues.The expressions of miR-155 and SOCS1 between PTC and normal thyroid tissues were analyzed,and its correlation with PTC clinical pathology was also analyzed.Results The expression of miR-155 in PTC was higher than that in normal thyroid tissue,while lower than that in normal thyroid tissue,and both of the differences were statistically significant(P<0.05).The expression of miR-155 and SOCS1 in PTC pathological grading,TNM stages and lymph node metastasis in patients were all related(P<0.05),while it had no correlation with the factors like gender,age and tumor size(P>0.05).The expressions of miR-155 and SOCS1 in PTC were negatively correlated(r=-0.564,P<0.05).Conclusion Abnormal expressions of miR-155 and SOCS1 in PTC were observed,and the expression increase of miR-155 may participate in the development of PTC through regulating the expression of SOCS1.Both miR-155 and SOCS1 could be become the new treatment targets of PTC.
作者 郭小卫 张卓昵 权明明 戴岳楚 GUO Xiao-wei;ZHANG Zhuo-ni;QUAN Ming-ming;DAI Yue-chu(Thyroid and Breast Surgery,Taizhou Hospital of Traditional Chinese Medicine,Taizhou,Zhejiang 318000,China)
出处 《中国卫生检验杂志》 CAS 2019年第8期914-916,920,共4页 Chinese Journal of Health Laboratory Technology
关键词 甲状腺乳头状癌 MIR-155 细胞因子信号转导抑制因子1 Thyroid papillary carcinoma miR-155 Suppressor of cytokine signaling-1
  • 相关文献

参考文献3

二级参考文献54

  • 1Michael W.Y. Chan,Eagle S.H. Chu,Ka-Fai To,Wai K. Leung. Quantitative detection of methylated SOCS-1, a tumor suppressor gene, by a modified protocol of quantitative real time methylation-specific PCR using SYBR green and its use in early gastric cancer detection[J] 2004,Biotechnology Letters(16):1289~1293
  • 2Shi B,Sepp-Lorenzino L,Prisco M,et ai.Micro RNA 145 targets the in- sulin receptor substrate-1 and inhibits the growth of colon cancer cells[J].J Biol Chem,2007,282(45):32582-32590.
  • 3Lim LP,Lau NC,Garrett-Engele P,et al.Microarray analysis shows that some microRNAs downregulate large number of target mRNAs[J].Na- ture,2005,433(7027):769-773.
  • 4Kong W,He L,Coppola M,et al.MicroRNA-155 regulates cell sur- vival,growth,and chemosensitivity by targeting F0X03a in breast cancer[J].J Biol Chem,2010,285(23):17869-17879.
  • 5Shibuya H,Linuma H,Shimada R,et al.Clinicalpathological and prognostic value of MicroRNA-21 and MicroRNA-155 in colorectal cancer[J].Oncology,2010,79(3):313-320.
  • 6Ryu JK,Hong SM,Karikari CA,et al.Aberrant raicroRNA-155 ex- pression is an early event in the multistep progression of pancreatic ade- nocarcinoma[J].Pancreatology,2010,10(1):66-73.
  • 7Giovannucci E.Insulin-like growth factor 1 and hinding protein-3 and risk of cancer[J].Horm Res,1999,51 Suppl3:34-41.
  • 8La Rocca G,Badin M,Shi B,et al.Mechanism of growth inhibition by MicroRNA 145:the role of the IGF-1 receptor signaling pathway[J].J Cell Physiol,2009,220(2):485491.
  • 9Jiang L,Liu X,Chen Zf et al.MicroRNA-7 targets IGFlR(insulin-like growth factor 1 receptor)in tongue squamous cell carcinoma cells[J].Biochem J,2010,432(1):199-205.
  • 10Leonard WJ, O'Shea JJ. Jaks and STATs: biological implications. Annu Rev Immunol, 1998, 16: 293-322.

共引文献16

同被引文献52

引证文献6

二级引证文献14

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