Roś-Mazurczyk Małgorzata, Wojakowska Anna, Marczak Łukasz, Polański Krzysztof, Pietrowska Monika, Polanska Joanna, Dziadziuszko Rafał, Jassem Jacek, Rzyman Witold, Widlak Piotr
Maria Skłodowska-Curie Memorial Cancer Center and Institute of Oncology, Gliwice, Poland.
Polish Academy of Science, Institute of Bioorganic Chemistry, Poznań, Poland.
Acta Biochim Pol. 2017;64(3):513-518. doi: 10.18388/abp.2017_1517. Epub 2017 Aug 12.
Blood biomarkers may support early diagnosis of lung cancer by enabling pre-selection of candidates for computed tomography screening or discrimination between benign and malignant screening-detected nodules. We aimed to identify features of serum metabolome distinguishing individuals with early-detected lung cancer from healthy participants of the lung cancer screening program.
Blood samples were collected in the course of a low-dose computed tomography screening program performed in the Gdansk district (Northern Poland). The analysis included 31 patients with screening-detected lung cancer and the pair-matched group of 92 healthy controls. The gas chromatography coupled to mass spectrometry (GC/MS) approach was used to identify and quantify small metabolites present in serum.
There were several metabolites detected in the sera whose abundances discriminated patients with lung cancer from controls. Majority of the differentiating components were downregulated in cancer samples, including amino acids, carboxylic acids and tocopherols, whereas benzaldehyde was the only compound significantly upregulated. A classifier including nine serum metabolites allowed separation of cancer and control samples with 100% sensitivity and 95% specificity.
Signature of serum metabolites discriminating between cancer patients and healthy participants of the early lung cancer screening program was identified using a GC/MS metabolomics approach. This signature, though not validated in an independent dataset, deserves further investigation in a larger cohort study.
血液生物标志物可通过对计算机断层扫描筛查的候选者进行预筛选或区分良性与恶性筛查发现的结节,来支持肺癌的早期诊断。我们旨在确定血清代谢组的特征,以区分早期发现肺癌的个体与肺癌筛查项目中的健康参与者。
在波兰北部格但斯克地区进行的低剂量计算机断层扫描筛查项目过程中采集血样。分析包括31例筛查发现肺癌的患者以及与之配对的92名健康对照者组成的小组。采用气相色谱-质谱联用(GC/MS)方法来鉴定和定量血清中存在的小分子代谢物。
在血清中检测到了几种代谢物,其丰度可区分肺癌患者与对照者。大多数有差异的成分在癌症样本中下调,包括氨基酸、羧酸和生育酚,而苯甲醛是唯一显著上调的化合物。一个包含九种血清代谢物的分类器能够以100%的灵敏度和95%的特异性区分癌症样本和对照样本。
使用GC/MS代谢组学方法确定了区分早期肺癌筛查项目中癌症患者与健康参与者的血清代谢物特征。尽管该特征尚未在独立数据集中得到验证,但值得在更大规模的队列研究中进一步研究。