期刊文献+

多肿瘤抑制基因1在口腔黏膜癌前病变和鳞癌中的变异 被引量:2

The alteration of MTS1 gene in precancerous lesions and squamous cell carcinoma of oral mucosa
原文传递
导出
摘要 目的 检测多肿瘤抑制基因 1(multipletumorsuppressor 1,MTS1)基因在口腔黏膜癌前病变和鳞癌中的表达和变异 (纯合性缺失和突变 )情况 ,以期发现MTS1在口腔黏膜恶变发生发展中的作用。方法 采用免疫组化SP法检测MTS1的表达情况 ;同时采用PCR、SSCP技术检测相同标本中MTS1基因exon1和exon2的纯合性缺失和突变情况。结果 口腔癌前病变中MTS1基因全部表达 ,无基因缺失和突变。鳞癌中MTS1的表达阳性率 6 0 % ;有 10例发生exon1和 (或 )exon2的纯合性缺失 ,4例基因突变 ,总变异率为 31.1% (14 / 4 5 ) ;伴有局部淋巴结转移的鳞癌的基因变异率为5 7.1% ,不伴有淋巴结转移的为 8.3% ,两者间差异有显著性 (P <0 .0 5 )。结论 MTS1基因在口腔癌前病变中无改变 ,不能作为检测口腔癌前病变的生物学指标 ;MTS1基因改变在口腔鳞癌的发生。 Objective To investigate the expression and alteration(including homozygous deletion and mutation) of MTS1 gene in precancerous lesions and squamous cell carcinomas(SCC) of oral mucosa, and to analyse the function of MTS1 gene alteration in oral mucosal carcinogenesis. Methods The expression of p16 protein producted by MTS1 gene was examined with immunohistochemical SP method in 10 normal oral mucosas, 30 precancerous lesions(10 mild, 10 moderate and 10 severe dysplasia respectively )and 45 squamous cell carcinomas(SCCⅠ18, SCCⅡ 19, SCCⅢ 8). The deletion and mutation of exon1 and exon2 of MTS1 gene were examined with methods of PCR and SSCP in these same samples. Results All the precancerous lesions had p16 protein expression and no alteration of MTS1 gene. In SCC,the positive rate of p16 protein was 60.0% with 72.2% in SCCⅠ,57.9% in SCCⅡ,37.5% in SCC Ⅲ ,and there were no significant difference among the three groups by χ 2 test(P>0.05).Gene homozygous deletion of exon1 and/or exon2 was detected in 10 cases, and gene mutation in 4 cases. The whole rate of gene alteration was 31.1%(14/45).The MTS1 gene alteration rate was 27.8% in SCCⅠ, 31.6% in SCCⅡ, 37.5% in SCC Ⅲ and there was also no significant difference among the three groups by χ 2 test(P>0.05).In SCC with local lymph nodes metastasis,MTS1 alteration rate was 57.1%,while in SCC with no lymph nodes metastasis was 8.3%, and there was significant difference by χ 2 test(P<0.05). Conclusions MTS1 gene alteration is not an early event in the carcinogenesis of oral mucosa and can not be used as a biology mark to examine oral precancerous lesions. MTS1 gene may play a certain role in the progression of oral squamous cell carcinomas.
出处 《中华口腔医学杂志》 CAS CSCD 北大核心 2003年第5期361-363,I004,共4页 Chinese Journal of Stomatology
基金 山东省自然科学基金资助项目 (Q97C0 412 8)
关键词 多肿瘤抑制基因1 MTS1 口腔黏膜癌 鳞癌 基因变异 肿瘤 Carcinoma, squamous cell Precancerous condition Genes,p16 Mutation
  • 相关文献

同被引文献12

  • 1郭小玲,孙善珍,魏奉才.涎腺腺样囊性癌p16基因失活机制的研究[J].华西口腔医学杂志,2005,23(5):418-420. 被引量:7
  • 2董玉英,王洁,董福生,王旭,张英怀,郭立华.口腔颊癌p16INK4/CDKN2基因的纯合子缺失与点突变[J].华西口腔医学杂志,2006,24(4):362-365. 被引量:4
  • 3Herman JG,Graff JR,Myohanen S,et al. Methylation-specific PCR: A novel PCR assay for methylation status of CpG island[J]. Proc Natl Acad Sci USA,1996,93(18):9821-9826.
  • 4Mirella GZ,Christina MB,Allen SY,et al. Methylation of 5'CpG island of the p16/CDKN2 tumor suppressor gene in normal and transformed human tissues correlates with gene silencing[J].Cancer Res,1995,55(20):4531-4535.
  • 5Minoru T,Coty H,Nito A,et al.Identification of differentially methylated sequences in colorectal cancer by methylated CpG island amplification[J].Cancer Res,1999,59(9):2307-2312.
  • 6Montserrat SC,Manel E,Li W,et al.Gene promoter hypermethylation in tumors and serum of head and neck cancer patients[J].Cancer Res,2000,60(4):892-895.
  • 7Lin SC,Chang KW,Chang CS,et al.Alterations of p16/MTS1 gene in oral squamous cell carcinomas from Taiwan Residents[J].J Oral Pathol Med,2000,29(4):159-163.
  • 8Hasegawa M,Nelson HH,Peters E,et al.Patterns of gene promoter methylation in squamous cell cancer of the head and neck[J].Oncogene,2002,21(37):4231-4236.
  • 9Tripathi Bhar A,Banerjee S,Chunder N,et al.Differential alterations of the genes in the CDKN2A-CCND1-CDK4-RB1 pathway are associated with the development of head and neck squamous cell carcinoma in Indian patients[J].J Cancer Res Clin Oncol,2003,129(11):642-650.
  • 10Esteller M,Corn PG,Baylin SB,et al.A gene hypermethylation profile of human cancer[J].Cancer Res,2001,61(8):3225-3229.

引证文献2

二级引证文献7

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