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首页> 外文期刊>British Journal of Cancer >Prognostic significance of nm23-H1 expression in oral squamous cell carcinoma
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Prognostic significance of nm23-H1 expression in oral squamous cell carcinoma

机译:nm23-H1表达在口腔鳞状细胞癌中的预后意义

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摘要

Recent studies indicated nm23-H1 played a role in cancer progression. Therefore, we investigated clinical significance of nm23-H1 expression in oral squamous cell carcinoma (OSCC). In total, 86 OSCC specimens were immunohistochemically stained with nm23-H1-specific monoclonal antibodies. Immunohistochemical staining of nm23-H1 was confirmed by immunoblotting. The relations between nm23-H1 expression and clinicopathologic variables were evaluated by χ2 analysis. As increased size of primary tumour could escalate metastatic potential and the data of patients at the late T stage might confound statistical analyses, we thus paid special attention to 54 patients at the early T stage of OSCC. Statistical difference of survival was compared by a log-rank test. Immunohistochemically, nm23-H1 expression was detected in 48.8% (42 out of 86) of tumorous specimens. It positively correlated with larger primary tumour size (P=0.03) and inversely with cigarette-smoking habit (P=0.042). In patients at the early T stage, decreased nm23 expression was associated with increased incidence of lymph node metastasis (P=0.004) and indicated poor survival (P=0.014). Tumour nm23-H1 expression is a prognostic factor for predicting better survival in OSCC patients at the early T stage, which may reflect antimetastatic potential of nm23. Therefore, modulation of nm23-H1 expression in cancer cells can provide a novel possibility of improving therapeutic strategy at this stage. In addition, our results further indicated cigarette smoking could aggravate the extent of nm23-H1 expression and possibly disease progression of OSCC patients.
机译:最近的研究表明nm23-H1在癌症进展中起作用。因此,我们调查了nm23-H1在口腔鳞状细胞癌(OSCC)中的表达的临床意义。总共用nm23-H1特异性单克隆抗体对86个OSCC标本进行了免疫组织化学染色。通过免疫印迹证实了nm23-H1的免疫组织化学染色。通过χ2分析评估nm23-H1表达与临床病理变量之间的关系。由于原发肿瘤的增大可能会增加转移潜力,并且T晚期患者的数据可能会混淆统计分析,因此,我们特别关注OSCC T早期54例患者。通过对数秩检验比较生存的统计学差异。免疫组织化学检测,在肿瘤标本中有48.8%(86个中的42个)中检测到nm23-H1表达。它与较大的原发肿瘤大小呈正相关(P = 0.03),与吸烟习惯呈负相关(P = 0.042)。在T早期的患者中,nm23表达的降低与淋巴结转移的发生率增加相关(P = 0.004),并且表明生存期较差(P = 0.014)。肿瘤nm23-H1表达是预测OSCC患者在T早期更好生存的预后因素,这可能反映了nm23的抗转移潜力。因此,在癌细胞中调节nm23-H1表达可以为改善这一阶段的治疗策略提供新的可能性。此外,我们的结果进一步表明,吸烟可能会加重nm23-H1表达的程度,并可能加剧OSCC患者的疾病进展。

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