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Clinical and genomic characteristics of metabolic syndrome in colorectal cancer

机译:结肠直肠癌代谢综合征的临床和基因组特征

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摘要

Metabolic syndrome (MetS) is characterized by a group of metabolic disturbances which leads to the enhanced risk of cancer development. Elucidating the mechanisms between these two pathologies is essential to identify the potential therapeutic molecular targets for colorectal cancer (CRC). 716 colorectal patients from the First and Second Affiliated Hospital of Wenzhou Medical University were involved in our study and metabolic disorders were proven to increase the risk of CRC. The prognostic value of the MetS factors was analyzed using the Cox regression model and a clinical MetS-based nomogram was established. Then by using multi-omics techniques, the distinct molecular mechanism of MetS genes in CRC was firstly systematically characterized. Strikingly, MetS genes were found to be highly correlated with the effectiveness of targeted chemotherapy administration, especially for mTOR and VEGFR pathways. Our results further demonstrated that overexpression of MetS core gene IL6 would promote the malignancy of CRC, which was highly dependent on mTOR-S6K signaling. In conclusion, we comprehensively explored the clinical value and molecular mechanism of MetS in the progression of CRC, which may serve as a candidate option for cancer management and therapy in the future.
机译:代谢综合征(METS)的特征在于一组代谢干扰,这导致癌症发育的风险增强。阐明这两种病理学之间的机制对于鉴定结直肠癌(CRC)的潜在治疗分子靶标是必不可少的。 716来自温州医科大学第一和第二附属医院的患者参与我们的研究,并证明了代谢障碍以增加CRC的风险。使用COX回归模型分析了METS因子的预后价值,并建立了临床科学的纳米图集图。然后通过使用多OMICS技术,首先系统地表征了CRC中的MetS基因的不同分子机制。令人惊讶的是,发现MetS基因与靶向化疗给药的有效性高度相关,特别是对于MTOR和VEGFR途径。我们的结果进一步证明了Mets核心基因IL6的过表达将促进CRC的恶性肿瘤,这高度依赖于MTOR-S6K信号传导。总之,我们全面探索了CRC进展中METS的临床价值和分子机制,可作为未来癌症管理和治疗的候选方案。

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