Wang Y-F, Chow K-C, Chang S-Y, Chiu J-H, Tai S-K, Li W-Y, Wang L-S
Department of Otolaryngology, Taipei Veterans General Hospital, National Yang-Ming University, Taipei 112, Taiwan, ROC.
Br J Cancer. 2004 Jun 1;90(11):2186-93. doi: 10.1038/sj.bjc.6601808.
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 chi(2) 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.
近期研究表明nm23-H1在癌症进展中发挥作用。因此,我们研究了nm23-H1表达在口腔鳞状细胞癌(OSCC)中的临床意义。总共86例OSCC标本用nm23-H1特异性单克隆抗体进行免疫组织化学染色。nm23-H1的免疫组织化学染色通过免疫印迹法得到证实。通过卡方分析评估nm23-H1表达与临床病理变量之间的关系。由于原发肿瘤大小增加会使转移潜能升高,且晚期T期患者的数据可能会混淆统计分析,因此我们特别关注了54例处于OSCC早期T期的患者。通过对数秩检验比较生存的统计学差异。免疫组织化学检测发现,86例肿瘤标本中有48.8%(42例)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)。在早期T期患者中,nm23表达降低与淋巴结转移发生率增加相关(P=0.004),并提示生存较差(P=0.014)。肿瘤nm23-H1表达是预测早期T期OSCC患者更好生存的一个预后因素,这可能反映了nm23的抗转移潜能。因此,调节癌细胞中nm23-H1的表达可以为改善现阶段的治疗策略提供一种新的可能性。此外,我们的结果进一步表明吸烟会加重nm23-H1的表达程度,并可能加剧OSCC患者的疾病进展。