Li Shaomin, Wang Rui, Zhang Mingxin, Wang Lina, Cheng Shaoli
World J Surg Oncol. 2013 Aug 5;11:173. doi: 10.1186/1477-7819-11-173.
Non-small cell lung cancer (NSCLC) accounts for more than 80% of all lung cancers, and reliable biomarkers are desirable. The present investigation assesses our ability to identify tumor relevant proteins from NSCLC tissue interstitial fluid (TIF).
Paired TIF was collected from three NSCLC patients at the time of surgery, and resolved by two-dimensional gel electrophoresis and in-gel digestion for proteomic analysis. Differentially expressed spots were extracted from the two-dimensional gel and characterized by high-performance liquid chromatography-tandem mass spectrometry. Then, ELISA was used to verify the expression of peroxiredoxin 1 (PRDX1) in TIF of patients with NSCLC and benign lung disease. Finally, the relationship between expression of PRDX1 and clinicopathological features was determined.
Comparative proteomic analysis showed 24 protein spots were differentially expressed with significant changes, including 11 upregulated proteins and 13 downregulated proteins. Of these, PRDX1 was selected for validation in TIF by Western blot and expression of PRDX1 was confirmed to be upregulated in tumor TIF. It was also demonstrated that PRDX1 was significantly elevated in 40 NSCLC patients with a mean level of 36.0 ng/mL compared to 6.26 ng/mL from 20 patients with benign lung disease. A significant correlation was found between the high level of PRDX1 expression and lymph node metastasis and tumor differentiation.
PRDX1 might be correlated with lymph node metastasis and differentiation, and its elevated expression in TIF may be an adverse biomarker for patients with NSCLC. PRDX1 may be attributed to the malignant transformation of NSCLC, and attention should be paid to a possible target for therapy.
非小细胞肺癌(NSCLC)占所有肺癌的80%以上,因此需要可靠的生物标志物。本研究评估了我们从NSCLC组织间质液(TIF)中鉴定肿瘤相关蛋白的能力。
在手术时从三名NSCLC患者中收集配对的TIF,并通过二维凝胶电泳和胶内消化进行蛋白质组分析。从二维凝胶中提取差异表达的斑点,并通过高效液相色谱-串联质谱进行表征。然后,使用酶联免疫吸附测定(ELISA)验证NSCLC患者和良性肺病患者TIF中过氧化物还原酶1(PRDX1)的表达。最后,确定PRDX1表达与临床病理特征之间的关系。
比较蛋白质组分析显示,有24个蛋白斑点差异表达且变化显著,其中11个蛋白上调,13个蛋白下调。其中,选择PRDX1通过蛋白质印迹法在TIF中进行验证,并证实PRDX1在肿瘤TIF中表达上调。还证实,40例NSCLC患者的PRDX1显著升高,平均水平为36.0 ng/mL,而20例良性肺病患者的PRDX1平均水平为6.26 ng/mL。PRDX1高表达水平与淋巴结转移和肿瘤分化之间存在显著相关性。
PRDX1可能与淋巴结转移和分化相关,其在TIF中的表达升高可能是NSCLC患者的不良生物标志物。PRDX1可能与NSCLC的恶性转化有关,应关注其作为可能的治疗靶点。