期刊文献+

肺癌肿瘤抑制因子-1在喉鳞癌组织中的表达及其意义

Expression of tumor suppressor in lung cancer 1 in laryngeal squamous cell carcinoma and its significance
原文传递
导出
摘要 目的研究肺癌肿瘤抑制因子-1(TSLC1)在喉鳞癌组织和癌旁正常组织的表达,探讨TSLC1与喉鳞癌的相关性,以期为喉癌的病因、诊断及治疗提供理论依据。方法取喉鳞状细胞癌组织标本蜡块45例,其中8例有淋巴结转移。取20例癌旁正常组织标本蜡块作为对照。应用免疫组化PV-6000二步法测定二者中TSLC1的表达,分析TSLC1的表达水平与各临床病理参数的关系。结果用SPSS 10.0统计软件进行统计学分析。结果 TSLC1在喉鳞癌标本中的阳性表达率为17/45(37.8%),明显低于癌旁正常组织中TSLC1的阳性表达率15/20(75.0%),二者比较差异有统计学意义(χ~2=7.68,P〈0.01)。TSLC1的表达下降与喉鳞癌的临床分期、分化程度、淋巴结转移情况差异有统计学意义(χ~2=4.15、6.11、4.11,P〈0.05),而与年龄、发病部位及性别差异无统计学意义(χ~2=0.25、0.09、1.0,P〉0.05)。结论 TSLC1在喉鳞癌中表达下降,且与喉鳞癌的临床分期、分化程度、淋巴结转移情况有相关性。TSLC1在喉鳞癌中的表达下降可能与喉鳞癌的发生和侵袭有关,但需扩大样本进一步研究。 Objective To investigate the correlation of tumor suppressor in lung cancer 1 (TSLC1)and laryngeal squa-mous cell carcinoma,in order to provide a theoretic basis of oncogenesis,diagnosis and treatment of laryngeal cancer. Methods Paraffin-embedded specimens were collected from 45 cases of laryngeal squamous cell carcinoma,8 of which had lymphatic metastasis.Another 20 specimens from normal adjacent tissues served as controls.The expression of TSLC1 was detected with immunohistochemical staining (PV-6000).The relation between TSLC1 expression and other clinicopathological parameters was analyzed with SPSS 10.0.Results The positive expression of TSLC1 was 17 /45 (37.8%)in specimens of laryngeal squamous cell carcinoma,which was significantly lower than in specimens of normal adjacent tissues (15 /20,75%),(χ2 =7.68,P 〈0.01 ).Loss of TSLC1 expression was correlated with the clinical stage,tumor differentiation and lymph node metastasis (χ2 =4.15,6.11,4.11,P 〈0.05 ),but not correlated with patients’age,gender,or location of primary laryngeal carcinoma (χ2 =0.25,0.09,1.0,P 〉0.05). Conclusion Loss of TSLC1 expression is frequently observed in laryngeal squamous cell carcinoma,which is signifi-cantly correlated to the clinical stage,tumor differentiation and lymph node metastasis.The down-regulation of TSLC1 expression may correlate with the occurrence and invasion of laryngeal squamous cell carcinoma,but more studies are needed to verify the hypothesis.
作者 李富 赵书佑
出处 《山东大学耳鼻喉眼学报》 CAS 2015年第6期36-38,42,共4页 Journal of Otolaryngology and Ophthalmology of Shandong University
关键词 喉鳞状细胞癌 肺癌肿瘤抑制因子-1 免疫组织化学 Laryngeal carcinoma Tumor suppressor in lung cancer 1 Immunohistochemistry
  • 相关文献

二级参考文献100

  • 1[1]Tamura G,Kihana T,Nomura K,Terada M,Sugimura T,Hirohashi S.Detection of frequent p53 gene mutations in primary gastric cancer by cell sorting and polymerase chain reaction single-strand conformation polymorphism analysis.Cancer Res 1991; 51:3056-3058
  • 2[2]Becker KF,Atkinson MJ,Reich U,Becker I,Nekarda H,Siewert JR,Hofler H.E-cadherin gene mutations provide clues to diffuse type gastric carcinomas.Cancer Res 1994; 54:3845-3852
  • 3[3]Tamura G,Sakata K,Nishizuka S,Maesawa C,Suzuki Y,Iwaya T,Terashima M,Saito K,Satodate R.Inactivation of the E-cadherin gene in primary gastric carcinomas and gastric carcinoma cell lines.Jpn J Cancer Res 1996; 87:1153-1159
  • 4[4]Kim IJ,Kang HC,Shin Y,Park HW,Jang SG,Han SY,Lim SK,Lee MR,Chang HJ,Ku JL,Yang HK,Park JG.A TP53-truncating germline mutation (E287X) in a family with characteristics of both hereditary diffuse gastric cancer and LiFraumeni syndrome.J Hum Genet 2004; 49:591-595
  • 5[5]Guilford P,Hopkins J,Harraway J,McLeod M,McLeod N,Harawira P,Taite H,Scoular R,Miller A,Reeve AE.E-cadherin germline mutations in familial gastric cancer.Nature 1998; 392:402-405
  • 6[6]Tamura G,Yin J,Wang S,Fleisher AS,Zou T,Abraham JM,Kong D,Smolinski KN,Wilson KT,James SP,Silverberg SG,Nishizuka S,Terashima M,Motoyama T,Meltzer SJ.E-Cadherin gene promoter hypermethylation in primary human gastric carcinomas.JNatl Cancer Inst 2000; 92:569-573
  • 7[7]Nishizuka S,Tamura G,Terashima M,Satodate R.Loss of heterozygosity during development and progression of differentiated adenocarcinoma of the stomach.J Pathol 1998;185:3843
  • 8[8]Akiyama Y,Nakasaki H,Nihei Z,Iwama T,Nomizu T,Utsunomiya J,Yuasa Y.Frequent microsatellite instabilities and analyses of the related genes in familial gastric cancers.Jpn J Cancer Res 1996; 87:595-601
  • 9[9]Semba S,Yokozaki H,Yasui W,Tahara E.Frequent microsatellite instability and loss of heterozygosity in the region including BRCA1 (17q21) in young patients with gastric cancer.Int J Oncol 1998; 12:1245-1251
  • 10[10]Tamura G,Sakata K,Maesawa C,Suzuki Y,Terashima M,Satoh K,Sekiyama S,Suzuki A,Eda Y,Satodate R.Microsatellite alterations in adenoma and differentiated adenocarcinoma of the stomach.Cancer Res 1995; 55:1933-1936

共引文献106

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