华西口腔医学杂志

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Twist在口腔鳞状细胞癌中的表达及其与 鳞状细胞癌上皮间质化的关系

孙昊轩1  冯红超2  宋宇峰3   

  1. 1.贵州医科大学附属口腔医院口腔颌面外科,贵阳 550004;2.贵阳市口腔医院,贵阳 550002;3.贵州省食品药品监督管理局,贵阳 550000
  • 收稿日期:2015-03-21 修回日期:2015-06-02 出版日期:2015-10-01 发布日期:2015-10-01
  • 通讯作者: 冯红超,主任医师,博士,E-mail:hongchaof@126.com
  • 作者简介:孙昊轩,住院医师,硕士,E-mail:805014760@qq.com
  • 基金资助:

    贵阳市卫生局科学技术计划基金资助项目(2014)

Expression of Twist and relation with epithelial-mesenchymal transition in oral squamous cell carcinoma

Sun Haoxuan1, Feng Hongchao2, Song Yufeng3.   

  1. 1. Dept. of Oral and Maxillofacial Surgery, Hospital of Stomatology, Guiyang Medical University, Guiyang 550004, China; 2. Guiyang Stomatological Hospital, Guiyang 550002, China; 3. Food and Drug Administration of Guizhou Province, Guiyang 550000, China
  • Received:2015-03-21 Revised:2015-06-02 Online:2015-10-01 Published:2015-10-01

摘要:

目的  观察人口腔鳞状细胞癌(OSCC)组织中上皮间质化相关蛋白及转录因子Twist的表达,研究Twist在OSCC上皮间质化中的作用及OSCC转移情况的相关性,并探讨其在人OSCC中的临床意义。方法  通过免疫组织化学及原位杂交的方法分别检测30例OSCC组织中上皮源性标记物E-钙黏蛋白(E-cad)和细胞角蛋白(CK),间质源性标记物N-钙黏蛋白(N-cad),转录因子Twist蛋白及mRNA的表达情况,并与临床病理资料作对照分析。结果  免疫组织化学结果:在OSCC组织中,Twist、N-cad的表达明显高于正常组织,E-cad及CK的表达明显低于正常组织(P<0.05);在OSCC中低分化组,Twist、N-cad的表达高于高分化组,E-cad及CK的表达明显低于高分化组(P<0.05);在有淋巴结转移组中,Twist、N-cad的表达高于无淋巴结转移组,E-cad及CK的表达低于无淋巴结转移组(P<0.05)。原位杂交结果:Twist mRNA在OSCC中低分化组,T3、T4组和有转移淋巴结组的表达分别高于高分化组,T1、T2组和无淋巴结转移组,以上差异均有统计学意义(P<0.05)。结论  OSCC组织中存在上皮间质化,Twist可使肿瘤细胞的侵袭力增加,促进OSCC的浸润和转移。联合检测Twist、E-cad和N-cad的表达可能会更有效地判断和预测OSCC的转移。

关键词: 口腔鳞状细胞癌, Twist, E-钙黏蛋白, 上皮间质化, 淋巴结转移

Abstract:

Objective  The objective of this paper was to study the expression of related protein and Twist transcription factor of epithelial-mesenchymal transition in oral squamous cell carcinoma (OSCC) tissue and the correlations of OSCC and oral squamous cell carcinometastasis. The paper also investigated the clinical significance of expression on OSCC. Methods  The labels of epithelium materialization (E-cadherin and cytokeratin), stromal labels (N-cadherin), transcription factor Twist protein, and mRNA expression in 30 OSCC tissues were investigated via immunohistochemistry and in situ hybridization. The paper also conducted contrast analysis with clinicopathology. Results  Immunization result showed that the expressions of Twist and N-cadherin in the OSCC group were more significant than those of the normal group (P<0.05). The expressions of E-cadherin and keratin in OSCC were significantly lower than those of the normal group (P<0.05). In the moderate- and low-differentiated group of OSCC, the expressions of Twist and N-cadherin were higher than those of the high-differentiated group (P<0.05). The expressions of E-cadherin and keratin were lower than those in the high-differentiated group (P<0.05). In the lymphatic metastasis group, the expressions of Twist and N-cadherin were higher than those of no-lymphatic metastasis group (P<0.05). The expressions of E-cadherin and keratin were lower than those of the no-lymphatic metastasis group (P<0.05). Results of in situ hybridization showed that the expression of Twist mRNA in the moderate- and low-differentiated groups of OSCC, T3, and T4 groups as well as that of the lymphatic metastasis group were higher than those of the high-differentiated, T1 and T2 groups, and no-separate lymphatic metastasis group, and the differences were statistically significant (P<0.05). Conclusion  Epithelium materialization exists in OSCC tissue. Twist can enhance the invasiveness of tumor cell and promote the infiltration and metastasis of OSCC. The combined detection of Twist, E-cadherin, and N-cadherin expressions can effectively predict and estimate OSCC metastasis.

Key words: oral squamous cell carcinoma, Twist, E-cadherin, epithelial-mesenchymal transition, lymph node metastasis