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Cdc42和WAVE1在非小细胞肺癌中的表达及临床病理意义
引用本文:韩文恒,张逊,徐美林,王菁,韩兴鹏,孙伟.Cdc42和WAVE1在非小细胞肺癌中的表达及临床病理意义[J].中国肿瘤临床,2013,40(23):1445-1449.
作者姓名:韩文恒  张逊  徐美林  王菁  韩兴鹏  孙伟
作者单位:①.天津医科大学(天津市 300070)
摘    要:  目的  探讨Cdc42和WAVE1在非小细胞肺癌(NSCLC)中的表达及其临床意义。  方法  采用免疫组织化学法检测106例经石蜡包埋的NSCLC组织及46例癌旁正常肺组织中Cdc42和WAVE1的表达情况。  结果  Cdc42和WAVE1在NSCLC组织中的表达明显高于正常肺组织。Cdc42的表达强度与肿瘤的分化程度、TNM分期及淋巴结转移情况之间差异有统计学意义(P < 0.05);WAVE1的表达强度与TNM分期及淋巴结转移情况之间差异有统计学意义(P < 0.05或P < 0.01)。NSCLC组织中Cdc42和WAVE1的表达呈正相关(r=0.469,P < 0.01)。Cdc42高表达组的3年生存率(44.16%)低于低表达组(72.41%),WAVE1高表达组的3年生存率(39.44%)亦低于低表达组(77.14%),且差异均有统计学意义(P < 0.01)。淋巴结转移、Cdc42和WAVE1共同高表达是影响NSCLC患者预后的独立因素。  结论  Cdc42和WAVE1在NSCLC组织中异常高表达,且呈现较好的相关性,可能共同参与并促进NSCLC的恶性进程,检测两者的表达会对NSCLC患者的临床病理学特征及预后起一定的提示作用。 

关 键 词:Cdc42    WAVE1    非小细胞肺癌    免疫组织化学
收稿时间:2013-05-27

Expression and clinicopathologic significance of Cdc42 and WAVE1 in non-small cell lung cancer
Affiliation:①.Tianjin Medical University, Tianjin 300070, China②.Department of Thoracic Surgery, Tianjin Chest Hospital, Tianjin 300051, China③.Department of Pathology, Tianjin Chest Hospital, Tianjin 300051, China
Abstract:  Objective  To investigate the expression and clinical significance of cell division cycle 42 (Cdc42) and WASP family verprolin-homologous protein l (WAVE1) in non–small cell lung cancer (NSCLC).  Methods  The expression of Cdc42 and WAVE1 was detected in 106 paraffin-embedded NSCLC tissues and 46 adjacent normal lung tissues (control group) using immunohistochemistry.  Results  The expression levels of Cdc42 and WAVE1 was distinctly higher in NSCLC than in the control group. The expression of Cdc42 in NSCLC significantly correlated with tumor differentiation, TNM stage, and lymph node metastasis (P < 0.05). The expression of WAVE1 in NSCLC was significantly correlated with TNM stage and lymph node metastasis (P < 0.05 or P < 0.01). The expression of Cdc42 was significantly correlated with WAVE1 in NSCLC (r=0.469, P < 0.01). The 3-year survival rates were significantly lower in the group with high Cdc42 expression (44.16%) than in the low expression group (72.41%; P < 0.01). Similarly, the 3-year survival rates were significantly lower among patients with high WAVE1 expression (39.44%) than in those with low expression (77.14%; P < 0.01). Lymph node metastasis and the common high Cdc42 and WAVE1 expression were independent prognostic factors for NSCLC.  Conclusion  The Cdc42 expression is correlated with WAVE1 expression. They may act together and have an important function in NSCLC. The expression of both Cdc42 and WAVE1 in NSCLC tissue may be used as markers for assessing the clinicopathologic features and prognosis. 
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