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非小细胞肺癌血清肽组特征的鉴定

Identification of Serum Peptidome Signatures of Non-Small Cell Lung Cancer.

作者信息

Klupczynska Agnieszka, Swiatly Agata, Hajduk Joanna, Matysiak Jan, Dyszkiewicz Wojciech, Pawlak Krystian, Kokot Zenon J

机构信息

Department of Inorganic and Analytical Chemistry, Poznan University of Medical Sciences, Grunwaldzka 6 Street, 60-780 Poznan, Poland.

Department of Thoracic Surgery, Poznan University of Medical Sciences, Szamarzewskiego 62 Street, 60-569 Poznan, Poland.

出版信息

Int J Mol Sci. 2016 Mar 31;17(4):410. doi: 10.3390/ijms17040410.

DOI:10.3390/ijms17040410
PMID:27043541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4848884/
Abstract

Due to high mortality rates of lung cancer, there is a need for identification of new, clinically useful markers, which improve detection of this tumor in early stage of disease. In the current study, serum peptide profiling was evaluated as a diagnostic tool for non-small cell lung cancer patients. The combination of the ZipTip technology with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) for the analysis of peptide pattern of cancer patients (n = 153) and control subjects (n = 63) was presented for the first time. Based on the observed significant differences between cancer patients and control subjects, the classification model was created, which allowed for accurate group discrimination. The model turned out to be robust enough to discriminate a new validation set of samples with satisfactory sensitivity and specificity. Two peptides from the diagnostic pattern for non-small cell lung cancer (NSCLC) were identified as fragments of C3 and fibrinogen α chain. Since ELISA test did not confirm significant differences in the expression of complement component C3, further study will involve a quantitative approach to prove clinical utility of the other proteins from the proposed multi-peptide cancer signature.

摘要

由于肺癌的高死亡率,需要鉴定新的、具有临床应用价值的标志物,以改善该肿瘤在疾病早期的检测。在当前研究中,血清肽谱分析被评估为非小细胞肺癌患者的一种诊断工具。首次展示了将ZipTip技术与基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF-MS)相结合,用于分析癌症患者(n = 153)和对照受试者(n = 63)的肽谱。基于在癌症患者和对照受试者之间观察到的显著差异,创建了分类模型,该模型能够准确区分不同组。结果表明该模型足够稳健,能够以令人满意的灵敏度和特异性区分新的验证样本集。非小细胞肺癌(NSCLC)诊断模式中的两种肽被鉴定为C3和纤维蛋白原α链的片段。由于ELISA试验未证实补体成分C3表达的显著差异,进一步的研究将采用定量方法来证明所提出的多肽癌症标志物中其他蛋白质的临床应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3258/4848884/d01063c9a8a7/ijms-17-00410-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3258/4848884/d01063c9a8a7/ijms-17-00410-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3258/4848884/d01063c9a8a7/ijms-17-00410-g001.jpg

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