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三维生长揭示了增殖途径对癌症中 5-脂氧合酶的精细调控。

Three-dimensional growth reveals fine-tuning of 5-lipoxygenase by proliferative pathways in cancer.

机构信息

Institute of Pharmaceutical Chemistry, Goethe University, Frankfurt, Germany.

Institute of Clinical Pharmacology, Pharmazentrum Frankfurt, ZAFES, Goethe University, Frankfurt, Germany.

出版信息

Life Sci Alliance. 2023 Feb 27;6(5). doi: 10.26508/lsa.202201804. Print 2023 May.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f64/9971161/2afae68d7406/LSA-2022-01804_Fig1.jpg

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