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NM23基因及其在口腔鳞状细胞癌中的表达。

The NM23 gene and its expression in oral squamous cell carcinoma.

作者信息

Lo Muzio L, Mignogna M D, Pannone G, Staibano S, Procaccini M, Serpico R, De Rosa G, Scully C

机构信息

Division of Oral Medicine and Pathology, University of Naples Federico II, Faculty of Medicine, Naples, Italy.

出版信息

Oncol Rep. 1999 Jul-Aug;6(4):747-51. doi: 10.3892/or.6.4.747.

Abstract

The murine nm23, a putative metastasis suppressor, has three human homologues, NM23-H1, -H2, and -H3b. Several reports have suggested a low metastatic potential for neoplasms with a high expression of NM23-H1 gene, while other studies have not shown this relationship. These apparent differences in the role of NM23 in metastasis suppression might be explained by unability to discriminate between the expression of the two genes NM23-H1 and NM23-H2. The NM23-H2 product is not related to tumor progression and metastasis suppression. Two studies on human oral squamous cell carcinoma (OSCC) have been reported, both showing the NM23 product to be a metastasis suppressor factor. However, none of these two studies distinguished NM23-H1 from NM23-H2. The aim of this study was to detect the protein expression pattern of NM23-H1 product in 24 OSCCs by immunohistochemistry in paraffin-embedded tissues using a monoclonal antibody non-cross-reactive with NM23-H2. The NM23-H1 positive group showed lower frequency of lymph node metastasis, and a better grading than the NM23-H1 negative group supporting the role of NM23-H1 as metastasis suppressor factor which may be useful for predicting tumor metastasis in OSCC.

摘要

小鼠nm23是一种假定的转移抑制因子,有三种人类同源物,即NM23-H1、-H2和-H3b。一些报告表明,NM23-H1基因高表达的肿瘤转移潜能较低,而其他研究并未显示出这种关系。NM23在转移抑制作用中这些明显的差异可能是由于无法区分NM23-H1和NM23-H2这两个基因的表达所致。NM23-H2产物与肿瘤进展和转移抑制无关。已有两项关于人类口腔鳞状细胞癌(OSCC)的研究报告,均表明NM23产物是一种转移抑制因子。然而,这两项研究均未区分NM23-H1和NM23-H2。本研究的目的是通过免疫组织化学方法,在石蜡包埋组织中使用与NM23-H2无交叉反应的单克隆抗体,检测24例OSCC中NM23-H1产物的蛋白表达模式。NM23-H1阳性组的淋巴结转移频率较低,分级优于NM23-H1阴性组,支持NM23-H1作为转移抑制因子的作用,这可能有助于预测OSCC中的肿瘤转移。

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