Wang Xin-Yun, Liu Ting, Zhu Cong-Zhong, Li Yan, Sun Rui, Sun Cui-Yun, Wang Ai-Xiang
Department of Pathology, Tianjin Medical University, Tianjin, P.R. China.
Ai Zheng. 2005 Sep;24(9):1091-5.
BACKGROUND & OBJECTIVE: The genesis, development, invasion, and metastasis of tumor are closely correlate with alterations of multi-genes. At present, the roles of Kang-ai-1 (KAI1), motility-related protein-1 (MRP-1), and focal adhesion kinase (FAK) in lung cancer have seldom been reported. This study was designed to investigate the roles of KAI1, MRP-1, and FAK in tumorigenesis and development of lung cancer, and their values in diagnosis and predicting the prognosis of lung cancer.
The expression of KAI1, MRP-1, and FAK proteins in a high-density tissue microarray containing 240 spots were detected by SP immunohistochemistry.
The positive rates of KAI1 and MRP-1 were significantly lower in primary lung cancer than in normal lung tissue (25.9% vs. 100%, 42.6% vs. 100%, P<0.05). The positive rate of FAK was significantly higher in primary lung cancer than in normal lung tissue (44.4% vs. 10.0%, P<0.05). The expression of KAI1, FAK, and MRP-1 in primary lung cancer had no correlation with age and gender of the patients, and macroscopic and histological type of tumor, but had correlations with tumor differentiation, clinical stage, and lymph node metastasis. In addition, the expression of MRP-1 had correlation with histological type of tumor; the positive rate of MRP-1 was significantly lower in small cell lung cancer than in non-small cell lung cancer (0 vs. 50.0%, P<0.05). KAI1 expression was negatively correlated to FAK expression (rs=-0.458, P<0.05); MRP-1 expression was positively correlated with KAI1 expression (rs=0.535, P<0.05), and negatively correlated with FAK expression (rs=-0.438, P<0.05).
The abnormal expression of KAI1, MRP-1, and FAK proteins are related to invasion and metastasis of lung cancer. Combined detection of the 3 proteins may be useful in predicting the development and prognosis of lung cancer.
肿瘤的发生、发展、侵袭及转移与多基因改变密切相关。目前,抗癌-1(KAI1)、运动相关蛋白-1(MRP-1)和黏着斑激酶(FAK)在肺癌中的作用鲜有报道。本研究旨在探讨KAI1、MRP-1和FAK在肺癌发生发展中的作用及其在肺癌诊断和预后预测中的价值。
采用SP免疫组织化学法检测含240个点的高密度组织芯片中KAI1、MRP-1和FAK蛋白的表达。
原发性肺癌中KAI1和MRP-1的阳性率显著低于正常肺组织(25.9%对100%,42.6%对100%,P<0.05)。原发性肺癌中FAK的阳性率显著高于正常肺组织(44.4%对10.0%,P<0.05)。原发性肺癌中KAI1、FAK和MRP-1的表达与患者的年龄、性别以及肿瘤的大体和组织学类型无关,但与肿瘤分化、临床分期及淋巴结转移有关。此外,MRP-1的表达与肿瘤组织学类型有关;小细胞肺癌中MRP-1的阳性率显著低于非小细胞肺癌(0对 50.0%,P<0.05)。KAI1表达与FAK表达呈负相关(rs=-0.458,P<0.05);MRP-1表达与KAI1表达呈正相关(rs=0.535,P<0.05),与FAK表达呈负相关(rs=-0.438,P<0.05)。
KAI1、MRP-1和FAK蛋白的异常表达与肺癌的侵袭和转移有关。联合检测这3种蛋白可能有助于预测肺癌的发展及预后。