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联合使用循环肿瘤细胞和唾液mRNA检测非小细胞肺癌。

Combined use of circulating tumor cells and salivary mRNA to detect non-small-cell lung cancer.

作者信息

Gu Xianwen, He Junfeng, Ji Guanglei

机构信息

The First Department of Thoracic Surgery.

The Second Department of Abdominal Surgery, Linyi Cancer Hospital, Shandong, China.

出版信息

Medicine (Baltimore). 2020 Feb;99(8):e19097. doi: 10.1097/MD.0000000000019097.

Abstract

Liquid biopsy is an emerging technique for noninvasive detection of various cancers. Majority of liquid biopsy tests still, however, use solitary type of biomarkers with unsatisfactory sensitivity and specificity. To this end, a combined approach of circulating tumor cells (CTCs) and salivary mRNA biomarkers was evaluated for discriminating non-small-cell lung cancer (NSCLC) from healthy controls.Our study included a discovery phase to find multiple biomarkers, and an independent validation phase to confirm the applicability of the selected biomarkers. In the discovery phase, CTC level in blood and 5 mRNA biomarkers in saliva (i.e., CCNI, Epidermal growth factor receptor [EGFR], FGF19, FRS2, and GREB1) were measured for 140 NSCLC patients and 140 healthy controls, followed by developing a predictive model. Next, this panel of biomarkers was applied to another patient cohort consisted of 60 patients with NSCLC and 60 healthy controls in the validation phase.We found that our novel biomarker panel could differentiate patients with NSCLC from healthy controls with high sensitivity (92.1%) and high specificity (92.9%) in the discovery phase. In the validation phase, we achieved sensitivity of 88.3% and specificity of 90.0%.To our best knowledge, it is the first time that a combined use of CTC and salivary mRNA biomarkers were applied for noninvasive detection of NSCLC.

摘要

液体活检是一种用于各种癌症无创检测的新兴技术。然而,大多数液体活检检测仍使用单一类型的生物标志物,其敏感性和特异性不尽人意。为此,我们评估了循环肿瘤细胞(CTC)和唾液mRNA生物标志物的联合方法,以区分非小细胞肺癌(NSCLC)与健康对照。我们的研究包括一个发现多种生物标志物的探索阶段和一个确认所选生物标志物适用性的独立验证阶段。在探索阶段,对140例NSCLC患者和140例健康对照测量了血液中的CTC水平和唾液中的5种mRNA生物标志物(即CCNI、表皮生长因子受体[EGFR]、FGF19、FRS2和GREB1),随后建立了一个预测模型。接下来,在验证阶段,将这组生物标志物应用于另一个由60例NSCLC患者和60例健康对照组成的患者队列。我们发现,在探索阶段,我们新的生物标志物组合能够以高敏感性(92.1%)和高特异性(92.9%)区分NSCLC患者与健康对照。在验证阶段,我们实现了88.3%的敏感性和90.0%的特异性。据我们所知,这是首次将CTC和唾液mRNA生物标志物联合用于NSCLC的无创检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d7f/7034687/072deaf6bca8/medi-99-e19097-g003.jpg

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