Combined targeting of senescent cells and senescent macrophages: A new idea for integrated treatment of lung cancer

IF 12.1 1区 医学 Q1 ONCOLOGY Seminars in cancer biology Pub Date : 2024-08-29 DOI:10.1016/j.semcancer.2024.08.006
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Abstract

Lung cancer is one of the most common cancers worldwide and a leading cause of cancer-related deaths. Macrophages play a key role in the immune response and the tumour microenvironment. As an important member of the immune system, macrophages have multiple functions, including phagocytosis and clearance of pathogens, modulation of inflammatory responses, and participation in tissue repair and regeneration. In lung cancer, macrophages are considered to be the major cellular component of the tumor-associated inflammatory response and are closely associated with tumorigenesis, progression and metastasis. However, macrophages gradually undergo a senescence process with age and changes in pathological states. Macrophage senescence is an important change in the functional and metabolic state of macrophages and may have a significant impact on lung cancer development. In lung cancer, senescent macrophages interact with other cells in the tumor microenvironment (TME) by secreting senescence-associated secretory phenotype (SASP) factors, which can either promote the proliferation, invasion and metastasis of tumor cells or exert anti-tumor effects through reprogramming or clearance under specific conditions. Therefore, senescent macrophages are considered important potential targets for lung cancer therapy. In this paper, a systematic review of macrophages and their senescence process, and their role in tumors is presented. A variety of inhibitory strategies against senescent macrophages, including enhancing autophagy, inhibiting SASP, reducing DNA damage, and modulating metabolic pathways, were also explored. These strategies are expected to improve lung cancer treatment outcomes by restoring the anti-tumor function of macrophages.

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联合靶向衰老细胞和衰老巨噬细胞:综合治疗肺癌的新思路。
肺癌是全球最常见的癌症之一,也是癌症相关死亡的主要原因。巨噬细胞在免疫反应和肿瘤微环境中发挥着关键作用。作为免疫系统的重要成员,巨噬细胞具有多种功能,包括吞噬和清除病原体、调节炎症反应以及参与组织修复和再生。在肺癌中,巨噬细胞被认为是肿瘤相关炎症反应的主要细胞成分,与肿瘤的发生、发展和转移密切相关。然而,随着年龄的增长和病理状态的变化,巨噬细胞会逐渐经历衰老过程。巨噬细胞衰老是巨噬细胞功能和代谢状态的重要变化,可能对肺癌的发生发展有重要影响。在肺癌中,衰老巨噬细胞通过分泌衰老相关分泌表型(SASP)因子与肿瘤微环境(TME)中的其他细胞相互作用,这些因子既可以促进肿瘤细胞的增殖、侵袭和转移,也可以在特定条件下通过重编程或清除发挥抗肿瘤作用。因此,衰老巨噬细胞被认为是肺癌治疗的重要潜在靶点。本文系统综述了巨噬细胞及其衰老过程,以及它们在肿瘤中的作用。本文还探讨了多种抑制衰老巨噬细胞的策略,包括增强自噬、抑制 SASP、减少 DNA 损伤和调节代谢途径。这些策略有望通过恢复巨噬细胞的抗肿瘤功能来改善肺癌治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Seminars in cancer biology
Seminars in cancer biology 医学-肿瘤学
CiteScore
26.80
自引率
4.10%
发文量
347
审稿时长
15.1 weeks
期刊介绍: Seminars in Cancer Biology (YSCBI) is a specialized review journal that focuses on the field of molecular oncology. Its primary objective is to keep scientists up-to-date with the latest developments in this field. The journal adopts a thematic approach, dedicating each issue to an important topic of interest to cancer biologists. These topics cover a range of research areas, including the underlying genetic and molecular causes of cellular transformation and cancer, as well as the molecular basis of potential therapies. To ensure the highest quality and expertise, every issue is supervised by a guest editor or editors who are internationally recognized experts in the respective field. Each issue features approximately eight to twelve authoritative invited reviews that cover various aspects of the chosen subject area. The ultimate goal of each issue of YSCBI is to offer a cohesive, easily comprehensible, and engaging overview of the selected topic. The journal strives to provide scientists with a coordinated and lively examination of the latest developments in the field of molecular oncology.
期刊最新文献
Extracellular vesicles and biomarker discovery cGAS/STING signalling pathway in senescence and oncogenesis Combined targeting of senescent cells and senescent macrophages: A new idea for integrated treatment of lung cancer Editorial Board Erratum to “RNA regulatory mechanisms controlling TGF-β signaling and EMT in cancer” [Semin. Cancer Biol. 102–103 (2024) 4–16]
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