刘维贤, 钟丽芳, 王天祥, 王秋旭. 舌鳞癌中uPA及nm23-H1蛋白表达及临床意义[J]. 中国肿瘤临床, 2006, 33(22): 1300-1302.
引用本文: 刘维贤, 钟丽芳, 王天祥, 王秋旭. 舌鳞癌中uPA及nm23-H1蛋白表达及临床意义[J]. 中国肿瘤临床, 2006, 33(22): 1300-1302.
Liu Weixian, Zhong Lifang, Wang Tianxiang, Wang Qiuxu. The Expression and Significance of uPA and nm23-H1 in Tongue Squamous Cell Cancer[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2006, 33(22): 1300-1302.
Citation: Liu Weixian, Zhong Lifang, Wang Tianxiang, Wang Qiuxu. The Expression and Significance of uPA and nm23-H1 in Tongue Squamous Cell Cancer[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2006, 33(22): 1300-1302.

舌鳞癌中uPA及nm23-H1蛋白表达及临床意义

The Expression and Significance of uPA and nm23-H1 in Tongue Squamous Cell Cancer

  • 摘要: 目的:探讨uPA及nm23-H1在舌鳞癌中的表达及与侵袭、转移的关系。方法:采用免疫组织化学方法在蛋白水平检测uPA及nm23-H1在74例舌癌中的表达。结果:uPA及nm23-H1与舌癌的病理学分级无关。uPA表达与肿瘤颈淋巴结转移呈正相关。nm23-H1表达与肿瘤颈淋巴结转移呈负相关。uPA及nm23-H1的表达率呈负相关。uPA阳性并且nm23-H1阴性表达者,颈淋巴结转移率明显高于uPA阴性并且nm23-H1阳性表达者。结论:uPA及nm23-H1的表达可以作为舌癌淋巴结转移的重要标志;uPA及nm23-H1的表达在舌癌的侵袭转移中可能是一对相互拮抗的因素,联合检测具有一定的临床意义。

     

    Abstract: Objective: To reveal the relationship between the expression and tumor behavior, such as invasion and metastasis in tongue squamous cell carcinoma (TSCC), by analyzing expression of the urokinase-type plasminogen (uPA) and nm23-H1. Methods: The expression of uPA and nm23-H1 at protein level was examined in 74 cases of TSCC using strep avidin-bi-otin complex (SABC) immunohistochemical technique. Results: The expression of uPA and nm-23 H1 showed a negative correlation with tumor pathological grade. The expression of uPA was positively related to cervical lymph-node metastasis. The expression of nm23-H1 was negatively related to cervical lymph-node metastasis. The expression of uPA had a negative correlation with the expression of nm23-H1. The TSCC cases with uPA(+)/nm23-H1 (-) revealed a significant higher tendency of cervical lymph-node metastasis compared to the uPA(-)/nm23-H1(+) group. Conclusions: The results obtained indicate that uPA and nm23-H1 protein may be an important biological marker in invasion and lymph-node metastasis of the TSCC.

     

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