Northwest Metabolomics Research Center, Seattle, WA, USA.
Department of Anesthesiology and Pain Medicine, Mitochondria and Metabolism Center, University of Washington, Seattle, WA, USA.
Metabolomics. 2024 Oct 5;20(5):112. doi: 10.1007/s11306-024-02179-y.
Cancer cells exhibit remarkable metabolic plasticity, enabling them to adapt to fluctuating nutrient conditions. This study investigates the impact of a combination of low glucose levels and inhibition of stearoyl-CoA desaturase 1 (SCD1) using A939572 on cancer metabolic plasticity and growth.
A comprehensive metabolomic and lipidomic analysis was conducted to unravel the intricate changes in cellular metabolites and lipids. MCF-7 cells were subjected to low glucose conditions, and SCD1 was inhibited using A939572. The resulting alterations in metabolic pathways and lipid profiles were explored to elucidate the synergistic effects on cancer cell physiology.
The combination of low glucose and A939572-induced SCD1 inhibition significantly impaired cancer cell metabolic plasticity. Metabolomic analysis highlighted shifts in key glycolytic and amino acid pathways, indicating the cells' struggle to adapt to restricted glucose availability. Lipidomic profiling revealed alterations in lipid composition, implying disruptions in membrane integrity and signaling cascades.
Our findings underscore the critical roles of glucose availability and SCD1 activity in sustaining cancer metabolic plasticity and growth. Simultaneously targeting these pathways emerges as a promising strategy to impede cancer progression. The comprehensive metabolomic and lipidomic analysis provides a detailed roadmap of molecular alterations induced by this combination treatment, that may help identify potential therapeutic targets.
癌细胞表现出显著的代谢可塑性,使它们能够适应不断变化的营养条件。本研究探讨了低葡萄糖水平和使用 A939572 抑制硬脂酰辅酶 A 去饱和酶 1(SCD1)对癌症代谢可塑性和生长的综合影响。
进行了全面的代谢组学和脂质组学分析,以揭示细胞代谢物和脂质的复杂变化。将 MCF-7 细胞置于低葡萄糖条件下,并使用 A939572 抑制 SCD1。探索代谢途径和脂质谱的变化,以阐明对癌细胞生理学的协同作用。
低葡萄糖和 A939572 诱导的 SCD1 抑制的组合显著损害了癌症细胞的代谢可塑性。代谢组学分析强调了关键糖酵解和氨基酸途径的变化,表明细胞在适应有限葡萄糖供应方面的困难。脂质组学分析显示脂质组成的改变,暗示了膜完整性和信号级联的破坏。
我们的研究结果强调了葡萄糖可用性和 SCD1 活性在维持癌症代谢可塑性和生长中的关键作用。同时针对这些途径是一种有前途的抑制癌症进展的策略。全面的代谢组学和脂质组学分析提供了这种组合治疗诱导的分子变化的详细路线图,可能有助于确定潜在的治疗靶点。