细胞角蛋白13和17在舌鳞癌和上皮发育不良中的表达

Sunaki Noguchi , Kazumichi Sato , Gou Yamamoto , Morio Tonogi , Yoichi Tanaka , Tetsuhiko Tachikawa , Gen-yuki Yamane
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引用次数: 8

摘要

目的探讨诊断上皮异常增生恶性潜能的因素。近年来的研究表明,检测细胞角蛋白13和17的表达对口腔鳞状细胞癌的早期诊断有重要意义。在本研究中,我们着重于基于上皮异常增生的恶性潜能进行诊断,并评估联合评估细胞角蛋白13和17的可行性。患者与方法采用实时荧光定量PCR和免疫组化染色对8例临床诊断为T1或T2舌鳞癌的患者进行细胞角蛋白13和17的表达分析。在每个标本的区域被确定为正常,不典型增生和癌症。结果实时荧光定量PCR结果显示,细胞角蛋白13的表达从发育不良开始降低,而细胞角蛋白17的表达从发育不良开始升高。免疫组化染色显示细胞角蛋白13阳性细胞从发育不良开始减少,而癌组织中几乎没有细胞角蛋白13阳性细胞。相反,细胞角蛋白17阳性细胞从发育不良开始增加,在癌症中几乎所有细胞都呈细胞角蛋白17阳性。因此,这些结果表明,细胞角蛋白13和17的表达与上皮发育不良的癌变有关。结论细胞角蛋白13和17的表达对上皮细胞发育不良的诊断有重要意义。此外,评估细胞角蛋白13和17的表达变化可以有效地评估手术边缘。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression of cytokeratin 13 and 17 in tongue squamous cell carcinoma and epithelial dysplasia

Objective

We have searched for the factor to diagnose malignant potential of epithelial dysplasia. Recent studies have suggested that determination of the expression of cytokeratin 13 and 17 would be useful for the early diagnosis of oral squamous cell carcinoma. In this study, we focused on the diagnosis based on the malignant potential of epithelial dysplasia and evaluated the feasibility of combined assessment of cytokeratin 13 and 17.

Patients and methods

The expression of cytokeratin 13 and 17 observed in 8 patients with clinically diagnosed T1 or T2 tongue squamous cell carcinoma was analyzed using real-time PCR and immunohistochemical staining of resected specimens. Areas in each specimen were identified as Normal, Dysplasia and Cancer.

Results

Real-time PCR showed that the expression of cytokeratin 13 decreased beginning with Dysplasia, whereas the expression of cytokeratin 17 increased beginning with Dysplasia. Immunohistochemical staining revealed that cytokeratin 13-positive cells decreased beginning with Dysplasia, while there were almost no cytokeratin 13-positive cells in Cancer. Conversely, cytokeratin 17-positive cells increased beginning with Dysplasia, and almost all cells were cytokeratin 17-positive in Cancer. These results thus indicate that the expression of cytokeratin 13 and 17 is associated with carcinogenesis in epithelial dysplasia.

Conclusions

The findings of this study indicate that assessment of the expression of cytokeratin 13 and 17 might be useful in the diagnosis of malignant potential in epithelial dysplasia. Moreover, evaluating changes in the expression of cytokeratin 13 and 17 could be effective in evaluating surgical margins.

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