Weber Daniel Gilbert, Johnen Georg, Casjens Swaantje, Bryk Oleksandr, Pesch Beate, Jöckel Karl-Heinz, Kollmeier Jens, Brüning Thomas
Institute for Prevention and Occupational Medicine of the German Social Accident Insurance, Institute of the Ruhr-Universität Bochum (IPA), Bürkle-de-la-Camp-Platz 1, 44789 Bochum, Germany.
BMC Res Notes. 2013 Dec 6;6:518. doi: 10.1186/1756-0500-6-518.
The long noncoding RNA MALAT1 (metastasis-associated lung adenocarcinoma transcript 1) is described as a potential biomarker for NSCLC (non-small cell lung cancer). Diagnostic biomarkers need to be detectable in easily accessible body fluids, should be characterized by high specificity, sufficient sensitivity, and robustness against influencing factors. The aim of this study was to evaluate the performance of MALAT1 as a blood based biomarker for NSCLC.
MALAT1 was shown to be detectable in the cellular fraction of peripheral human blood, showing different expression levels between cancer patients and cancer-free controls. For the discrimination of NSCLC patients from cancer-free controls a sensitivity of 56% was calculated conditional on a high specificity of 96%. No impact of tumor stage, age, gender, and smoking status on MALAT1 levels could be observed, but results based on small numbers.
The results of this study indicate that MALAT1 complies with key characteristics of diagnostic biomarkers, i.e., minimal invasiveness, high specificity, and robustness. Due to its relatively low sensitivity MALAT1 might not be feasible as a single biomarker for the diagnosis of NSCLC in the cellular fraction of blood. Alternatively, MALAT1 might be applicable as a complementary biomarker within a panel in order to improve the entire diagnostic performance.
长链非编码RNA MALAT1(转移相关的肺腺癌转录本1)被描述为非小细胞肺癌(NSCLC)的一种潜在生物标志物。诊断生物标志物需要在易于获取的体液中可检测到,应具有高特异性、足够的敏感性以及对影响因素的稳健性。本研究的目的是评估MALAT1作为NSCLC血液生物标志物的性能。
MALAT1在外周人血的细胞部分中可检测到,在癌症患者和无癌对照之间显示出不同的表达水平。对于区分NSCLC患者和无癌对照,在96%的高特异性条件下计算出的敏感性为56%。未观察到肿瘤分期、年龄、性别和吸烟状态对MALAT1水平有影响,但基于少量样本的结果。
本研究结果表明,MALAT1符合诊断生物标志物的关键特征,即微创性、高特异性和稳健性。由于其相对较低的敏感性,MALAT1作为血液细胞部分中NSCLC诊断的单一生物标志物可能不可行。或者,MALAT1可能作为一组中的补充生物标志物适用,以提高整体诊断性能。