Metabolomics Analysis of Functional Activity Changes in Residual Tumour Cells After IOCS Treatment

Lai-wei You, Jinhuo Wang, Dan Yin, Bao-ji Hu, Yong Cheng, Xue-fei Wang, Hao Li, Jianrong Guo
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Abstract

Hepatocellular carcinoma (HCC) is a serious and often lethal cancer, particularly in patients with chronic liver disease. Currently, no specific treatment has been utilised to prevent HCC. The detailed mechanism of HCC is still elusive, and this study aims to identify and characterise the functional activity changes in residual tumour cells following intraoperative cell salvage (IOCS) treatment during HCC surgery. This research is a retrospective case–control study, involving the selection of 60 patients with HCC who underwent radical surgery; then blood and tumour tissue were collected for further testing. GC–MS assay, immunofluorescence, Western blot and qRT-PCR techniques were employed. Our study found comparable demographic and baseline clinical characteristics between the experimental group (n = 30), which received IOCS treatment during surgery, and the control group (n = 30), which did not receive IOCS treatment, validating subsequent analyses. Metabolomic analysis revealed six key metabolites differing between groups, indicating improvement in liver tumours in the experimental group. TP53 expression was significantly upregulated, potentially mediating therapeutic effects. The intervention reduced HCC cell migration and apoptosis, decreased E2F1 and MDM2 protein and mRNA levels, and increased TP53 and CTNNB1 levels. These findings support the potential clinical application of the intervention in improving treatment outcomes for HCC patients, warranting further investigation to elucidate the underlying mechanisms and optimise therapeutic strategies.

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IOCS治疗后残余肿瘤细胞功能活性变化的代谢组学分析。
肝细胞癌(HCC)是一种严重且经常致命的癌症,特别是在慢性肝病患者中。目前,尚无专门的治疗方法用于预防HCC。HCC的具体机制尚不清楚,本研究旨在识别和表征HCC手术中术中细胞抢救(IOCS)治疗后残留肿瘤细胞的功能活性变化。本研究是一项回顾性病例对照研究,选取60例接受根治性手术的HCC患者;然后采集血液和肿瘤组织进行进一步检测。采用气相色谱-质谱、免疫荧光、Western blot、qRT-PCR等技术。我们的研究发现在手术期间接受IOCS治疗的实验组(n = 30)和未接受IOCS治疗的对照组(n = 30)之间具有可比性的人口统计学和基线临床特征,验证了随后的分析。代谢组学分析显示六种关键代谢物在两组之间存在差异,表明实验组的肝脏肿瘤有所改善。TP53表达显著上调,可能介导治疗效果。干预降低HCC细胞迁移和凋亡,降低E2F1和MDM2蛋白及mRNA水平,升高TP53和CTNNB1水平。这些发现支持了干预在改善HCC患者治疗结果方面的潜在临床应用,需要进一步研究以阐明潜在机制并优化治疗策略。
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期刊介绍: The Journal of Cellular and Molecular Medicine serves as a bridge between physiology and cellular medicine, as well as molecular biology and molecular therapeutics. With a 20-year history, the journal adopts an interdisciplinary approach to showcase innovative discoveries. It publishes research aimed at advancing the collective understanding of the cellular and molecular mechanisms underlying diseases. The journal emphasizes translational studies that translate this knowledge into therapeutic strategies. Being fully open access, the journal is accessible to all readers.
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