Institute of Pharmaceutical Chemistry, Goethe University, Frankfurt, Germany.
Institute of Clinical Pharmacology, Pharmazentrum Frankfurt, ZAFES, Goethe University, Frankfurt, Germany.
Life Sci Alliance. 2023 Feb 27;6(5). doi: 10.26508/lsa.202201804. Print 2023 May.
The leukotriene (LT) pathway is positively correlated with the progression of solid malignancies, but the factors that control the expression of 5-lipoxygenase (5-LO), the central enzyme in LT biosynthesis, in tumors are poorly understood. Here, we report that 5-LO along with other members of the LT pathway is up-regulated in multicellular colon tumor spheroids. This up-regulation was inversely correlated with cell proliferation and activation of PI3K/mTORC-2- and MEK-1/ERK-dependent pathways. Furthermore, we found that and its target gene were involved in the repression of 5-LO during cell proliferation. Importantly, we found that this PI3K/mTORC-2- and MEK-1/ERK-dependent suppression of 5-LO is also existent in tumor cells from other origins, suggesting that this mechanism is widely applicable to other tumor entities. Our data show that tumor cells fine-tune 5-LO and LT biosynthesis in response to environmental changes repressing the enzyme during proliferation while making use of the enzyme under cell stress conditions, implying that tumor-derived 5-LO plays a role in the manipulation of the tumor stroma to quickly restore cell proliferation.
白细胞三烯 (LT) 途径与实体恶性肿瘤的进展呈正相关,但控制肿瘤中 LT 生物合成的关键酶 5-脂氧合酶 (5-LO) 表达的因素知之甚少。在这里,我们报告 5-LO 及其 LT 途径的其他成员在多细胞结肠肿瘤球体中上调。这种上调与细胞增殖和 PI3K/mTORC-2 和 MEK-1/ERK 依赖性途径的激活呈负相关。此外,我们发现 和其靶基因 参与了细胞增殖过程中 5-LO 的抑制。重要的是,我们发现这种 PI3K/mTORC-2 和 MEK-1/ERK 依赖性的 5-LO 抑制在其他来源的肿瘤细胞中也存在,这表明这种机制广泛适用于其他肿瘤实体。我们的数据表明,肿瘤细胞根据环境变化精细调节 5-LO 和 LT 生物合成,在增殖期间抑制酶,而在细胞应激条件下利用酶,这意味着肿瘤衍生的 5-LO 在操纵肿瘤基质以快速恢复细胞增殖方面发挥作用。