高IGFL2通过Warburg效应调节卵巢癌进展和肿瘤免疫微环境。

IF 3.5 2区 生物学 Q3 CELL BIOLOGY
Zhizai Chen, Dalong Song, Shuting Huang, Jinyu Chao, Junhong Huang, Ming Luo, Shanyang He
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引用次数: 0

摘要

本研究旨在探讨胰岛素样生长因子样家族成员2 (IGFL2)在卵巢癌转移中的作用及机制。具体来说,我们关注的是IGFL2如何调节肿瘤细胞能量代谢,影响巨噬细胞极化促进卵巢癌转移。本研究通过体外和体内实验阐明IGFL2的生物学功能,旨在为卵巢癌治疗寻找新的治疗靶点,提供更有效的治疗策略。我们的研究发现,IGFL2在卵巢癌转移中表达显著上调,其高表达与卵巢癌的恶性和转移潜能呈正相关。IGFL2敲低促进线粒体氧化磷酸化,抑制Warburg效应,表现为氧消耗率(OCR)和ATP生成增加,糖酵解酶表达和乳酸分泌减少。同时,IGFL2通过STAT1/STAT6信号通路促进M2巨噬细胞极化,增加CD11b + CD206 + M2细胞比例,抑制M1极化。在体内,IGFL2敲低显著抑制异种移植物模型的肿瘤生长和代谢重编程。这些发现表明IGFL2通过调节代谢重编程(Warburg效应)和影响肿瘤相关巨噬细胞(TAM)极化的双重机制促进OC转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High IGFL2 regulates ovarian cancer progression and the tumor immune microenvironment via the Warburg effect.

This study aimed to explore the role and mechanism of insulin-like growth factor-like family member 2 (IGFL2) in ovarian cancer (OC) metastasis. Specifically, we focused on how IGFL2 regulates tumor cell energy metabolism and influences macrophage polarization to promote ovarian cancer metastasis. By conducting in vitro and in vivo experiments to elucidate the biological functions of IGFL2, this study aiming to identify new therapeutic targets for ovarian cancer treatment and provide a more effective treatment strategy. Our study revealed that the expression of IGFL2 was substantially upregulated in ovarian cancer metastases, and its high expression was positively correlated with the malignancy and metastatic potential of ovarian cancer. IGFL2 knockdown promoted mitochondrial oxidative phosphorylation and inhibited the Warburg effect, evidenced by increased oxygen consumption rate (OCR) and ATP production, and decreased glycolytic enzyme expression and lactate secretion. Concurrently, IGFL2 promoted M2 macrophage polarization via the STAT1/STAT6 signaling pathway, increasing the proportion of CD11b + CD206 + M2 cells and suppressing M1 polarization. In vivo, IGFL2 knockdown significantly inhibited tumor growth and metabolic reprogramming in xenograft models.These findings demonstrate that IGFL2 promotes OC metastasis through a dual mechanism: regulating metabolic reprogramming (Warburg effect) and influencing tumor-associated macrophage (TAM) polarization.

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来源期刊
Molecular and Cellular Biochemistry
Molecular and Cellular Biochemistry 生物-细胞生物学
CiteScore
8.30
自引率
2.30%
发文量
293
审稿时长
1.7 months
期刊介绍: Molecular and Cellular Biochemistry: An International Journal for Chemical Biology in Health and Disease publishes original research papers and short communications in all areas of the biochemical sciences, emphasizing novel findings relevant to the biochemical basis of cellular function and disease processes, as well as the mechanics of action of hormones and chemical agents. Coverage includes membrane transport, receptor mechanism, immune response, secretory processes, and cytoskeletal function, as well as biochemical structure-function relationships in the cell. In addition to the reports of original research, the journal publishes state of the art reviews. Specific subjects covered by Molecular and Cellular Biochemistry include cellular metabolism, cellular pathophysiology, enzymology, ion transport, lipid biochemistry, membrane biochemistry, molecular biology, nuclear structure and function, and protein chemistry.
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