PKAⅠ、HSP27及PTEN在口腔鳞癌组织中的表达及相关性研究  被引量:2

Expression and Significance of PKAⅠ,HSP27 and PTEN Protein in Oral Squamous Cell Carcinoma Significance

在线阅读下载全文

作  者:李善昌[1] 李业强[1] 刘芷君[1] 姜炳华[1] 闫磊[1] 宁尚波[1] 张铁军[1] 

机构地区:[1]佳木斯大学口腔医院口腔颌面外科,黑龙江佳木斯154002

出  处:《口腔医学研究》2013年第8期742-744,747,共4页Journal of Oral Science Research

基  金:黑龙江省自然基金(编号:D201025)

摘  要:目的:探讨口腔鳞状细胞癌(口腔鳞癌,OSCC)癌组织中PKAⅠ、HSP27及PTEN的表达情况及临床生物学上的相关意义。方法:应用免疫组化SP法检测50例口腔鳞癌组织及20例正常口腔组织中的PKAⅠ、HSP27及PTEN的表达情况。结果:PKAⅠ、HSP27在病例组中的阳性表达率(分别为72%、80%),明显高于对照组(正常组)(分别为25%、40%)(P<0.05)。PTEN的阳性表达率在病例组中24%,明显低于正常对照组60%(P<0.05)。PKAⅠ在口腔鳞癌中的表达与HSP27呈正向相关(r=0.4048,P<0.05),PKAⅠ与PTEN呈负向相关(r=-0.3796,P<0.05),HSP27与PTEN呈负向相关(r=-0.7727,P<0.05)。结论:PKAⅠ、HSP27在口腔鳞癌的发生、发展过程中可能起着协同促进的作用,而PTEN在口腔鳞癌的发生、发展过程中可能起着拮抗抑制PKAⅠ、HSP27的作用。三者均可作为诊断鳞癌的依据。Objective: To study the expression of PKA I , HSP27 and PTEN in oral squamous cell carcinoma and their clinical significance. Methods: The method of detectiving 50 patients with oral squamous cell carcinoma of PKA I , HSP27 and PTEN and 20 cases of normal oral tissues expression was SP method. Results: PKA I , HSP27 in the positive rate of OSCC (72%, 80%) were significantly higher than the normal oral mucosa(25%, 40%). PTEN expression in normal oral mucosa 60.00% and in the positive rate of oral squamous cell carcinoma was 24% which had a significant difference between groups. There was positive correlation between the PKA Ⅰ and HSP27 expression. However, There were inverse correlation between PKA Ⅰ and PTEN expression and inverse correlation between HSP27αand PTEN expression. Conclusion: PKA I , HSP27 in oral squamous cell carcinoma may play an collaborative role in the event of the development process. PTEN may antagonize PKA I , and HSP27 expression. They all cart be used as the basis for diagnosis of oral squamous cell carcinoma.

关 键 词:PKAⅠ HSP27 PTEN 口腔鳞癌 免疫组织化学 

分 类 号:R739.8[医药卫生—肿瘤]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象