Determination of volatile organic compounds in SW620 colorectal cancer cells and tumor-bearing mice

•Volatile organic compounds released by the human body have great potential in diagnosis and therapeutic monitoring for colorectal cancer.•Cancer is a metabolic disease in which metabolic changes are used to maintain a high rate of proliferation and resistance to cell death.•We analyze not only the...

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Veröffentlicht in:Journal of pharmaceutical and biomedical analysis 2019-04, Vol.167, p.30-37
Hauptverfasser: Wang, Guiyue, Li, Yuhang, Liu, Miao, Guo, Nana, Han, Ci, Liu, Desheng, Li, Dandan, Yang, Mengyuan, Peng, Yahui, Liu, Yansong, Yu, Kaijiang, Wang, Changsong
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Sprache:eng
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Zusammenfassung:•Volatile organic compounds released by the human body have great potential in diagnosis and therapeutic monitoring for colorectal cancer.•Cancer is a metabolic disease in which metabolic changes are used to maintain a high rate of proliferation and resistance to cell death.•We analyze not only the VOCs in model organism blood samples but also the VOCs in the headspace of colorectal cancer cell lines. Early diagnosis and early treatment are important factors in reducing colorectal cancer (CRC) metastasis and mortality. Volatile organic compounds (VOCs) released by the human body have great potential for use in clinical diagnosis and therapeutic monitoring for CRC. The aim of our study was to identify VOCs with high specificity and high sensitivity for CRC and to provide a method for early diagnosis of CRC. Gas chromatography-mass spectrometry (GC–MS) was utilized to analyze metabolites in both the in vivo and in vitro experimental groups. In vivo, VOCs were analyzed in the blood of mice after cell inoculation and tumor resection. In vitro experiments were performed by comparing changes in VOCs in an HCoEpiC cell group, control group, SW620 cell group and Arsenic trioxide + SW620 group. We observed changes in VOCs in a series of CRC SW620 cells in vivo and in vitro. Among these changes, we found that the concentrations of 8 substances, including acetone, increased with tumor growth. Nine substances were found to be significantly elevated in the SW620 cancer cell group compared with the other groups. Only one substance was consumed by the tumor in both the in vivo and in vitro experiments. Our study showed that alkanes, lipids, alcohols, ketones, aldehyde, butylated hydroxytoluene (BHT) and hexamethylcyclotrisiloxane all existed at different levels in SW620 CRC cells compared to those in normal cells. We need more research to further confirm this hypothesis.
ISSN:0731-7085
1873-264X
DOI:10.1016/j.jpba.2019.01.050