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肿瘤微环境中的蛋白质脂化:酶学、信号通路与治疗学

Protein lipidation in the tumor microenvironment: enzymology, signaling pathways, and therapeutics.

作者信息

Xu Mengke, Xu Bo

机构信息

Chongqing Key Laboratory of Intelligent Oncology for Breast Cancer, Intelligent Oncology Innovation Center Designated by the Ministry of Education, Chongqing University Cancer Hospital and Chongqing University School of Medicine, Chongqing, 400030, China.

出版信息

Mol Cancer. 2025 May 7;24(1):138. doi: 10.1186/s12943-025-02309-7.

Abstract

Protein lipidation is a pivotal post-translational modification that increases protein hydrophobicity and influences their function, localization, and interaction network. Emerging evidence has shown significant roles of lipidation in the tumor microenvironment (TME). However, a comprehensive review of this topic is lacking. In this review, we present an integrated and in-depth literature review of protein lipidation in the context of the TME. Specifically, we focus on three major lipidation modifications: S-prenylation, S-palmitoylation, and N-myristoylation. We emphasize how these modifications affect oncogenic signaling pathways and the complex interplay between tumor cells and the surrounding stromal and immune cells. Furthermore, we explore the therapeutic potential of targeting lipidation mechanisms in cancer treatment and discuss prospects for developing novel anticancer strategies that disrupt lipidation-dependent signaling pathways. By bridging protein lipidation with the dynamics of the TME, our review provides novel insights into the complex relationship between them that drives tumor initiation and progression.

摘要

蛋白质脂化是一种关键的翻译后修饰,它增加了蛋白质的疏水性,并影响其功能、定位和相互作用网络。新出现的证据表明脂化在肿瘤微环境(TME)中具有重要作用。然而,目前缺乏对该主题的全面综述。在本综述中,我们对肿瘤微环境背景下的蛋白质脂化进行了综合深入的文献综述。具体而言,我们重点关注三种主要的脂化修饰:S-异戊二烯化、S-棕榈酰化和N-肉豆蔻酰化。我们强调这些修饰如何影响致癌信号通路以及肿瘤细胞与周围基质细胞和免疫细胞之间的复杂相互作用。此外,我们探讨了靶向脂化机制在癌症治疗中的治疗潜力,并讨论了开发破坏脂化依赖性信号通路的新型抗癌策略的前景。通过将蛋白质脂化与肿瘤微环境的动态变化联系起来,我们的综述为驱动肿瘤发生和进展的它们之间的复杂关系提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c206/12057185/c4fab7102f99/12943_2025_2309_Fig1_HTML.jpg

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