Laboratory of Medical Genetics, Harbin Medical University, Baojian Road 157, Nangang District, Harbin 150081, China.
Mol Biol Rep. 2012 Mar;39(3):2697-703. doi: 10.1007/s11033-011-1024-7. Epub 2011 Jun 14.
Lung cancer is a leading cause of cancer-related death, about 40% human non-small cell lung cancer (NSCLC) patients showed lymph node involvements. However, the precise mechanism for the metastasis is still not fully understood. This study was to analyze the potential molecular mechanism for lung cancer metastasis. In the current study, proteomics analysis by two-dimensional electrophoresis (2-DE) was performed first to identify the differentially expressed protein between the higher metastasis lung adenocarcinoma cell line Anip973 and the lower metastasis lung adenocarcinoma cell line AGZY83-a. We confirmed the result by RT-PCR, immunoblotting and immunocytochemistry analyses in these two cell lines. Then we examined the expression of the differentially expressed protein in tumor tissues of NSCLC patients by immunoblotting and immunohistochemistry analyses. Using 2-DE analysis, we have identified DJ-1 was expressed higher in the higher metastasis Anip973 compared to the parental cell line AGZY83-a, that was confirmed by RT-PCR, immunoblotting and immunocytochemistry analyses. In NSCLC patients' tumor tissues study, immunoblotting data showed that, DJ-1 expression level was significantly higher in 72.2% (13/18) of NSCLC tissue samples compared to that in paired normal lung tissues (P = 0.044). Immunohistochemistry analysis demonstrated increased DJ-1 expression in 85 NSCLC tumor tissue samples compared with 7 normal lung tissue samples (P = 0.044). DJ-1 expression was also found to be significantly correlated with cancer lymphatic metastasis (P = 0.039). DJ-1 might contribute to the metastasis of NSCLC.
肺癌是癌症相关死亡的主要原因,约 40%的人类非小细胞肺癌(NSCLC)患者存在淋巴结受累。然而,转移的确切机制仍不完全清楚。本研究旨在分析肺癌转移的潜在分子机制。在本研究中,首先通过二维电泳(2-DE)进行蛋白质组学分析,以鉴定高转移肺腺癌细胞系 Anip973 和低转移肺腺癌细胞系 AGZY83-a 之间差异表达的蛋白质。我们通过这些两种细胞系的 RT-PCR、免疫印迹和免疫细胞化学分析验证了结果。然后,我们通过免疫印迹和免疫组织化学分析检测了 NSCLC 患者肿瘤组织中差异表达蛋白的表达。通过 2-DE 分析,我们已经确定 DJ-1 在高转移 Anip973 中的表达高于亲本细胞系 AGZY83-a,这通过 RT-PCR、免疫印迹和免疫细胞化学分析得到了证实。在 NSCLC 患者肿瘤组织研究中,免疫印迹数据显示,与配对的正常肺组织相比,72.2%(13/18)的 NSCLC 组织样本中 DJ-1 的表达水平显著升高(P=0.044)。免疫组织化学分析显示,与 7 个正常肺组织样本相比,85 个 NSCLC 肿瘤组织样本中 DJ-1 的表达增加(P=0.044)。DJ-1 的表达也与癌症淋巴转移显著相关(P=0.039)。DJ-1 可能有助于 NSCLC 的转移。