期刊文献+

食管鳞状细胞癌组织中hsa-miRNA-133a的表达变化及意义 被引量:1

Expression of hsa-miRNA-133a in esophageal squamous cell carcinoma and its significance
下载PDF
导出
摘要 目的观察hsa-miRNA-133a在食管鳞状细胞癌组织中的表达变化,探讨其与食管鳞状细胞癌临床病理参数的关系。方法采用miRNA流体芯片技术和Real-time PCR法检测食管鳞状细胞癌及癌旁组织中的hsa-miR-NA-133a,分析hsa-miRNA-133a的表达与食管鳞状细胞癌临床病理参数的关系。结果 hsa-miRNA-133a在食管鳞状细胞癌组织中的表达显著低于癌旁组织(P<0.05),低分化者肿瘤组织中hsa-miRNA-133a的表达低于中高分化者,肿瘤浸润至肌层、外膜者肿瘤组织中hsa-miRNA-133a的表达低于肿瘤位于黏膜内者(P均<0.05);hsa-miRNA-133a在不同肿瘤直径及有无淋巴结转移者中的表达差异无统计学意义(P均>0.05)。结论 hsa-miRNA-133a在食管鳞状细胞癌组织中呈低表达,可能与食管鳞状细胞癌的发生发展有关。 Objective To detect the expression of hsa-miRNA-133a in esophageal squamous cell carcinoma and to investigate its correlation with clinicopathological parameters.Method miRNA microfluidic chip technology and Real-time PCR were used to detect the expression of hsa-miRNA-133a in esophageal squamous cell carcinoma,and the correlation between the expression of hsa-miRNA-133a and clinicopathological parameters were analyzed.Results The expression of hsa-miRNA-133a was significantly lower in esophageal squamous cell carcinoma compared to adjacent tissue,with statistically significant difference(P 0.05).Low expression levels of hsa-miRNA-133a were associated with cancer invasion and tumor differentiation(P 0.05),but not associated with tumor size and lymph node metastasis(all P 0.05).Conclusion Hsa-miRNA-133a shows low expression in esophageal squamous cell carcinoma,which may be associated with the occurrence and development of esophageal squamous cell carcinoma.
出处 《山东医药》 CAS 2013年第18期19-21,共3页 Shandong Medical Journal
基金 江苏省自然科学基金面上研究项目(BK2012666)
关键词 微小RNA hsa-miRNA-133a 食管肿瘤 食管鳞状细胞癌 microRNA hsa-miRNA-133a esophageal neoplasms esophageal squamous cell carcinoma
  • 相关文献

参考文献15

  • 1Esquela-Kerscher A, Slack FJ. OncomiRNAs-microRNAs with a role in cancer[J]. Nat Rev Cancer, 2006,6(4) :259-269.
  • 2Parkin DM, Bray F, Ferlay J, et al. Estimating the world cancer burden : Globocan 2000 [ J ]. Int J Cancer, 2001,94 (2) : 153-156.
  • 3Zhang W, Bailey-Wilson JE, Li W, et al. Segregation analysis of esophageal cancer in a moderately high-incidence area of northern China[J]. Am J Hum Genet, 2000,67 (1) :110-119.
  • 4Volinia S, Calin GA, Liu CG, et al. A microRNA expression sig- nature of human solid tumors defines cancer gene targets[ J]. Proc Natl Acad Sci USA, 2006,103 (7) :2257-2261.
  • 5Chen WS, Leung CM, Pan HW, et al. Silencing of miRNA-I-1 and miRNA-133a-2 cluster expression by DNA hypermethylation in colorectal cancer[ J]. Oncol Rep, 2012,28 (3) : 1069-1076.
  • 6Suzuki S, Yokobori T, Tanaka N, et al. CD47 expression regulated by the miRNA-133a tumor suppressor is a novel prognostic marker in esophageal squamous cell carcinoma[ J]. Oncol Rep, 2012,28 (2) :465-472.
  • 7Chiyomaru T, Enokida H, Tatarano S, et al. miRNA-145 and miRNA-133a function as tumour suppressors and directly regulate FSCN1 expression in bladder cancer[ J]. Br J Cancer, 2010,102 (5) :883-891.
  • 8Nohata N, Hanazawa T, Kikkawa N, et al. Caveolin-1 mediates tumor cell migration and invasion and its regulation by miRNA- 133a in head and neck squamous cell carcinoma[ J]. Int J Oncol, 2011,38(1 ) :209-217.
  • 9Wu ZS, Wang CQ, Xiang R,et al. Loss of miR-133a expression associated with poor survival of breast cancer and restoration of miR-133a expression inhibited breast cancer cell growth and inva- sion[ J]. BMC Cancer, 2012,12:51.
  • 10Ruebel K, Leontovich AA, Stilling GA, et al. MicroRNA expres- sion in ileal carcinoid tumors: downregulation of microRNA-133a with tumor progression [ J ]. Mod Pathol, 2010,23 ( 3 ) : 367-375.

二级参考文献10

  • 1Chung HW,Lee SG,Kim H,et al.Serum high mobility group box-1 (HMGB1) is closely associated with the clinical and pathologic features of gastric cancer[J].J Transl Med,2009,7:38.
  • 2Kusume A,Sasahira T,Luo Y,et al.Suppression of dendritic cells by HMGB1 is associated with lymph node metastasis of human colon cancer[J].Pathobiology.2009,76(4):155-162.
  • 3Schoppmann SF,Bimer P,Studer P,et al.Lymphatic microvessel density and lymphovascular invasion assessed by anti-podoplanin immuostaining in human breast cancer[J].Anticancer Res,2001,21 (4A):2351-2355.
  • 4陈小平,石应康,段德生,主编.外科学[M].北京:人民卫生出版社,2002.480-484.
  • 5Pepper MS,Tille JC,Nisato R.Lymphangiogenesis and tumor metastasis[J].Cell Tissue Res,2003,314(1):167-177.
  • 6Padera TP,Kadambi A,Di Tomaso E,et al.Lymphatic metastasis in the absence of functional intratumor lymphatics[J].Science,2002,296(5574):1883-1886.
  • 7Fujii K,Luo Y,Sasahira T,et al.Co-treatment with deoxycholic acid and azoxymethane accelerates secretion of HMGB1 in IEC6 intestinal epithelial cells[J].Cell Prolif.2009,42(5):701-709.
  • 8Degryse B,Bonaldi T,Scaffidi P,et al.The high mobility group (HMG) boxes of the nuclear protein HMG1 induce chemotaxis and cytoskeleton reorganization in rat smooth muscle cells[J].J Cell Biol,2001,152(6):1197-1206.
  • 9Schlueter C,Weber H,Meyer B,et al.Angiogenetic signaling through hypoxia HMGB1:an angiogenetic switch molecule[J].Am J Pathol,2005,166(4):1259-1263.
  • 10陈传贵,于振涛.抗肿瘤治疗的新靶点—HMGB1[J].中国肿瘤临床,2009,36(2):114-117. 被引量:2

共引文献5

同被引文献3

引证文献1

二级引证文献6

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