Ahmed Naseer, Kidane Biniam, Wang Le, Nugent Zoann, Moldovan Nataliya, McElrea April, Shariati-Ievari Shiva, Qing Gefei, Tan Lawrence, Buduhan Gordon, Srinathan Sadeesh K, Meyers Renelle, Aliani Michel
CancerCare Manitoba Research Institute, Winnipeg, MB, Canada.
Department of Radiology, Section of Radiation Oncology, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.
Front Oncol. 2022 Jun 3;12:874964. doi: 10.3389/fonc.2022.874964. eCollection 2022.
Every year, close to two million people world-wide are diagnosed with and die of lung cancer. Most patients present with advanced-stage cancer with limited curative options and poor prognosis. Diagnosis of lung cancer at an early stage provides the best chance for a cure. Low- dose CT screening of the chest in the high-risk population is the current standard of care for early detection of lung cancer. However, CT screening is invasive due to radiation exposure and carries the risk of unnecessary biopsies in non-cancerous tumors. In this pilot study, we present metabolic alterations observed in sputum and breath condensate of the population of early- stage non-small cell lung cancer (NSCLC) patients cancer before and after surgical resection (SR), which could serve as noninvasive diagnostic tool. Exhaled breath condensate (EBC) (n=35) and sputum (n=15) were collected from early-stage non-small cell lung cancer (NSCLC) patients before and after SR. Median number of days for EBC and sputum collection before and after SR were 7 and 42; and 7 and 36 respectively Nuclear magnetic resonance (NMR) and liquid chromatography quadrupole time-of-flight mass spectrometry (LC-QTOF-MS) were used to analyze the metabolic profile of the collected samples. A total of 26 metabolites with significant alteration post SR were identified, of which 14 (54%) were lipids and 12 constituted nine different chemical metabolite classes. Eighteen metabolites (69%) were significantly upregulated and 8 (31%) were downregulated. Median fold change for all the up- and downregulated metabolites (LC-QTOF-MS) were 10 and 8, respectively. Median fold change (MFC) in concentration of all the up- and downregulated metabolites (NMR) were 0.04 and 0.27, respectively. Furthermore, glucose (median fold change, 0.01, p=0.037), adenosine monophosphate (13 log fold, p=0.0037) and N1, N12- diacetylspermine (8 log fold p=0.011) sputum levels were significantly increased post-SR. These identified sputa and EBC indices of altered metabolism could serve as basis for further exploration of biomarkers for early detection of lung cancer, treatment response, and targets for drug discovery. Validation of these promising results by larger clinical studies is warranted.
全球每年有近200万人被诊断出患有肺癌并死于肺癌。大多数患者就诊时已处于癌症晚期,治愈选择有限且预后不佳。肺癌的早期诊断提供了最佳的治愈机会。对高危人群进行胸部低剂量CT筛查是目前早期发现肺癌的标准治疗方法。然而,CT筛查因辐射暴露具有侵入性,并且存在对非癌性肿瘤进行不必要活检的风险。在这项初步研究中,我们展示了在手术切除(SR)前后早期非小细胞肺癌(NSCLC)患者群体的痰液和呼气冷凝物中观察到的代谢改变,这可以作为一种非侵入性诊断工具。在SR前后从早期非小细胞肺癌(NSCLC)患者中收集呼气冷凝物(EBC)(n = 35)和痰液(n = 15)。SR前后EBC和痰液收集的中位天数分别为7天和42天;以及7天和36天。使用核磁共振(NMR)和液相色谱四极杆飞行时间质谱(LC-QTOF-MS)分析所收集样本的代谢谱。共鉴定出26种在SR后有显著改变的代谢物,其中14种(54%)是脂质,12种构成9种不同的化学代谢物类别。18种代谢物(69%)显著上调,8种(31%)下调。所有上调和下调代谢物(LC-QTOF-MS)的中位变化倍数分别为10和8。所有上调和下调代谢物(NMR)浓度的中位变化倍数(MFC)分别为0.04和0.27。此外,SR后痰液中葡萄糖(中位变化倍数,0.01,p = 0.037)、单磷酸腺苷(13对数变化倍数,p = 0.0037)和N1,N12-二乙酰精胺(8对数变化倍数,p = 0.011)水平显著升高。这些确定的痰液和EBC代谢改变指标可以作为进一步探索肺癌早期检测生物标志物、治疗反应以及药物发现靶点的基础。有必要通过更大规模的临床研究对这些有前景的结果进行验证。