基于 UPLC-MS/MS 代谢组学研究雷帕霉素和 mTORC1/2 双抑制剂 OSI-027 对结肠癌细胞代谢的影响。

IF 3 3区 医学 Q2 ONCOLOGY Investigational New Drugs Pub Date : 2024-08-01 Epub Date: 2024-06-25 DOI:10.1007/s10637-024-01438-y
Kai Fan, Yueyuan Wang, Jiangyujing Bian, Yewen Sun, Jiaqi Dou, Jie Pan, Yunli Yu
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引用次数: 0

摘要

mTORC1/2双重抑制剂可能比mTORC1抑制剂雷帕霉素更有效。然而,它们对结肠癌细胞代谢的影响仍有待探索。我们对雷帕霉素和新型 OSI-027 在结肠癌细胞 HCT-116 中的抗增殖作用进行了比较分析,并通过超高效液相色谱-质谱联用仪(UPLC-MS/MS)评估了它们对代谢的影响。结果表明,与雷帕霉素相比,OSI-027 能更有效地抑制结肠癌细胞的增殖。此外,我们还从光谱中鉴定出了近 600 种代谢物,揭示了用 OSI-027 和雷帕霉素处理的细胞在代谢模式上的显著差异。通过 VIP 值筛选,我们确定了导致这些差异的关键代谢物。在抑制糖酵解和减少葡萄糖消耗方面,OSI-027 可能比雷帕霉素更有效。在氨基酸代谢方面,虽然OSI-027与雷帕霉素一样具有广泛的作用,但它们的作用程度并不完全相同。这些发现填补了有关mTORC1/2双重抑制剂的知识空白,为进一步开发和研究奠定了基础。
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Study on the effects of rapamycin and the mTORC1/2 dual inhibitor OSI-027 on the metabolism of colon cancer cells based on UPLC-MS/MS metabolomics.

mTORC1/2 dual inhibitors may be more effective than mTORC1 inhibitor rapamycin. However, their metabolic impacts on colon cancer cells remain unexplored. We conducted a comparative analysis of the anti-proliferative effects of rapamycin and the novel OSI-027 in colon cancer cells HCT-116, evaluating their metabolic influences through ultra-high performance liquid chromatography-mass spectrometry (UPLC-MS/MS). Our results demonstrate that OSI-027 more effectively inhibits colon cancer cell proliferation than rapamycin. Additionally, we identified nearly 600 metabolites from the spectra, revealing significant differences in metabolic patterns between cells treated with OSI-027 and rapamycin. Through VIP value screening, we pinpointed crucial metabolites contributing to these distinctions. For inhibiting glycolysis and reducing glucose consumption, OSI-027 was likely to be more potent than rapamycin. For amino acids metabolism, although OSI-027 has a broad effect as rapamycin, their effects in degrees were not exactly the same. These findings address the knowledge gap regarding mTORC1/2 dual inhibitors and lay a foundation for their further development and research.

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来源期刊
CiteScore
7.60
自引率
0.00%
发文量
121
审稿时长
1 months
期刊介绍: The development of new anticancer agents is one of the most rapidly changing aspects of cancer research. Investigational New Drugs provides a forum for the rapid dissemination of information on new anticancer agents. The papers published are of interest to the medical chemist, toxicologist, pharmacist, pharmacologist, biostatistician and clinical oncologist. Investigational New Drugs provides the fastest possible publication of new discoveries and results for the whole community of scientists developing anticancer agents.
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