Volatile organic compound analysis of malignant pleural mesothelioma chorioallantoic membrane xenografts.

IF 3.7 4区 医学 Q1 BIOCHEMICAL RESEARCH METHODS Journal of breath research Pub Date : 2024-09-11 DOI:10.1088/1752-7163/ad7166
Liam D Little, Sarah E Barnett, Theo Issitt, Sam Bonsall, Vikki A Carolan, Elizabeth Allen, Laura M Cole, Neil A Cross, Judy M Coulson, Sarah L Haywood-Small
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Abstract

Malignant pleural mesothelioma (MPM) is an aggressive cancer associated with asbestos exposure. MPM is often diagnosed late, at a point where limited treatment options are available, but early intervention could improve the chances of successful treatment for MPM patients. Biomarkers to detect MPM in at-risk individuals are needed to implement early diagnosis technologies. Volatile organic compounds (VOCs) have previously shown diagnostic potential as biomarkers when analysed in MPM patient breath. In this study, chorioallantoic membrane (CAM) xenografts of MPM cell lines were used as models of MPM tumour development for VOC biomarker discovery with the aim of generating targets for investigation in breath, biopsies or other complex matrices. VOC headspace analysis of biphasic or epithelioid MPM CAM xenografts was performed using solid-phase microextraction and gas chromatography-mass spectrometry. We successfully demonstrated the capture, analysis and separation of VOC signatures from CAM xenografts and controls. A panel of VOCs was identified that showed discrimination between MPM xenografts generated from biphasic and epithelioid cells and CAM controls. This is the first application of the CAM xenograft model for the discovery of VOC biomarkers associated with MPM histological subtypes. These findings support the potential utility of non-invasive VOC profiling from breath or headspace analysis of tissues for detection and monitoring of MPM.

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恶性胸膜间皮瘤绒毛膜异种移植物的挥发性有机化合物分析。
恶性胸膜间皮瘤(MPM)是一种与石棉暴露有关的侵袭性癌症。恶性胸膜间皮瘤通常诊断较晚,治疗方案有限,但早期干预可提高恶性胸膜间皮瘤患者治疗成功的几率。要实施早期诊断技术,就需要检测高危人群中 MPM 的生物标志物。在分析 MPM 患者呼气时,挥发性有机化合物 (VOC) 已显示出作为生物标记物的诊断潜力。在这项研究中,将 MPM 细胞系的绒毛膜(CAM)异种移植作为 MPM 肿瘤发展的模型,用于发现挥发性有机化合物生物标记物,目的是在呼气、活检或其他复杂基质中生成调查目标。我们采用固相微萃取和气相色谱-质谱法对双相MESO-7T、上皮样MESO-8T和MESO-12T MPM CAM异种移植物进行了挥发性有机化合物顶空分析。我们成功展示了从 CAM 异种移植物和对照组中捕获、分析和分离挥发性有机化合物特征的方法。鉴定出的一组挥发性有机化合物可区分由双相和上皮样细胞生成的 MPM 异种移植物和 CAM 对照组。这是首次应用 CAM 异种移植物模型发现与 MPM 组织学亚型相关的挥发性有机化合物生物标志物。这些发现支持了通过组织呼气或顶空分析进行非侵入性挥发性有机化合物分析以检测和监测 MPM 的潜在用途。
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来源期刊
Journal of breath research
Journal of breath research BIOCHEMICAL RESEARCH METHODS-RESPIRATORY SYSTEM
CiteScore
7.60
自引率
21.10%
发文量
49
审稿时长
>12 weeks
期刊介绍: Journal of Breath Research is dedicated to all aspects of scientific breath research. The traditional focus is on analysis of volatile compounds and aerosols in exhaled breath for the investigation of exogenous exposures, metabolism, toxicology, health status and the diagnosis of disease and breath odours. The journal also welcomes other breath-related topics. Typical areas of interest include: Big laboratory instrumentation: describing new state-of-the-art analytical instrumentation capable of performing high-resolution discovery and targeted breath research; exploiting complex technologies drawn from other areas of biochemistry and genetics for breath research. Engineering solutions: developing new breath sampling technologies for condensate and aerosols, for chemical and optical sensors, for extraction and sample preparation methods, for automation and standardization, and for multiplex analyses to preserve the breath matrix and facilitating analytical throughput. Measure exhaled constituents (e.g. CO2, acetone, isoprene) as markers of human presence or mitigate such contaminants in enclosed environments. Human and animal in vivo studies: decoding the ''breath exposome'', implementing exposure and intervention studies, performing cross-sectional and case-control research, assaying immune and inflammatory response, and testing mammalian host response to infections and exogenous exposures to develop information directly applicable to systems biology. Studying inhalation toxicology; inhaled breath as a source of internal dose; resultant blood, breath and urinary biomarkers linked to inhalation pathway. Cellular and molecular level in vitro studies. Clinical, pharmacological and forensic applications. Mathematical, statistical and graphical data interpretation.
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