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细胞外丙酮酸激酶M2通过调节巨噬细胞极性来调控癌症免疫。

Extracellular PKM2 modulates cancer immunity by regulating macrophage polarity.

作者信息

Peng Guangda, Li Bin, Han Hongwei, Yuan Yi, Mishra Falguni, Huang Yang, Liu Zhi-Ren

机构信息

Department of Biology, Georgia State University, University Plaza, Atlanta, GA, 30303, USA.

出版信息

Cancer Immunol Immunother. 2025 May 9;74(7):195. doi: 10.1007/s00262-025-04050-y.

Abstract

Tumor controls its immunity by educating its microenvironment, including regulating polarity of tumor associated macrophages. It is well documented that cancer cells release PKM2 to facilitate tumor progression. We report here that the extracellular PKM2 (EcPKM2) modulates tumor immunity by facilitating M2 macrophage polarization in tumors. EcPKM2 interacts with integrin αβ on macrophage to activate integrin-FAK-PI3K signal axis. Activation of FAK-PI3K by EcPKM2 suppresses PTEN expression, which subsequently upregulates arginase1 (Arg1) expression and activity in macrophage to facilitate M2 polarity. Our studies uncover a novel and important mechanism for modulation of tumor immunity. More importantly, an antibody against PKM2 that disrupts the interaction between EcPKM2 and integrin αβ is effective in converting M2 macrophages to M1 macrophages in tumors, suggesting a new therapeutic strategy and target for cancer therapies. Combination of the anti-PKM2 antibody with checkpoint blockades provides enhanced treatment effects.

摘要

肿瘤通过塑造其微环境来控制自身免疫,包括调节肿瘤相关巨噬细胞的极性。已有充分文献证明癌细胞会释放丙酮酸激酶M2(PKM2)以促进肿瘤进展。我们在此报告,细胞外PKM2(EcPKM2)通过促进肿瘤中M2巨噬细胞极化来调节肿瘤免疫。EcPKM2与巨噬细胞上的整合素αβ相互作用,激活整合素-黏着斑激酶(FAK)-磷脂酰肌醇-3-激酶(PI3K)信号轴。EcPKM2对FAK-PI3K的激活抑制了磷酸酶和张力蛋白同源物(PTEN)的表达,进而上调巨噬细胞中精氨酸酶1(Arg1)的表达和活性,以促进M2极化。我们的研究揭示了一种调节肿瘤免疫的新的重要机制。更重要的是,一种针对PKM2的抗体可破坏EcPKM2与整合素αβ之间的相互作用,能有效将肿瘤中的M2巨噬细胞转化为M1巨噬细胞,这为癌症治疗提出了一种新的治疗策略和靶点。抗PKM2抗体与检查点阻断剂联合使用可增强治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d06f/12064527/495df99c255c/262_2025_4050_Fig1_HTML.jpg

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