癌症
化学
胃肠病学
医学
内科学
胃内容物
丁基羟基甲苯
色谱法
胃
生物化学
抗氧化剂
作者
Linda Mežmale,Daria Ślefarska‐Wolak,Manohar Prasad Bhandari,Clemens Ager,Viktors Veliks,V. Patsko,Andrii Lukashenko,Emmanuel Dias‐Neto,Diana Noronha Nunes,Thais Fernanda Bartelli,Adriane Pelosof,Cláudia Zitron,Raúl Murillo,Agnieszka Królicka,Chris A. Mayhew,Mārcis Leja,Hossam Haick,Paweł Mochalski
标识
DOI:10.1088/1752-7163/ad324f
摘要
Volatilomics is a powerful tool capable of providing novel biomarkers for the diagnosis of gastric cancer. The main objective of this study was to characterize the volatilomic signatures of gastric juice in order to identify potential alterations induced by gastric cancer. Gas chromatography with mass spectrometric detection, coupled with headspace solid phase microextraction as the pre-concentration technique, was used to identify volatile organic compounds (VOCs) released by gastric juice samples collected from 78 gastric cancer patients and two cohorts of controls (80 and 96 subjects) from four different locations (Latvia, Ukraine, Brazil, and Colombia). 1440 distinct compounds were identified in samples obtained from patients and 1422 in samples provided by controls. However, only 6% of the VOCs exhibited an incidence higher than 20%. Amongst the volatiles emitted, 18 showed differences in their headspace concentrations above gastric juice of cancer patients and controls. Ten of these (1-propanol, 2,3-butanedione, 2-pentanone, benzeneacetaldehyde, 3-methylbutanal, butylated hydroxytoluene, 2-pentyl-furan, 2-ethylhexanal, 2-methylpropanal and phenol) appeared at significantly higher levels in the headspace of the gastric juice samples obtained from patients; whereas, eight species showed lower abundance in patients than found in controls. Given that the difference in the volatilomic signatures can be explained by cancer-related changes in the activity of certain enzymes or pathways, the former set can be considered potential biomarkers for gastric cancer, which may assist in developing non-invasive breath tests for the diagnosis of this disease. Further studies are required to elucidate further the mechanisms that underlie the changes in the volatilomic profile as a result of gastric cancer.
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