Guo Rongqi, Wang Rui, Zhang Weisong, Li Yangyang, Wang Yihao, Wang Hao, Li Xia, Song Jianxiang
Department of Thoracic Surgery, Affiliated Hospital 6 of Nantong University, Medical School of Nantong University, Nantong, PR China.
Department of Thoracic Surgery, Affiliated Hospital 6 of Nantong University, Yancheng Third People's Hospital, Yancheng, PR China.
Cancer Control. 2025 Jan-Dec;32:10732748251316604. doi: 10.1177/10732748251316604.
Macrophages are a critical component of the innate immune system, derived from monocytes, with significant roles in anti-inflammatory and anti-tumour activities. In the tumour microenvironment, however, macrophages are often reprogrammed into tumour-associated macrophages (TAMs), which promote tumour growth, metastasis, and therapeutic resistance.
To review recent advancements in the understanding of macrophage polarisation and reprogramming, highlighting their role in tumour progression and potential as therapeutic targets.
This is a review article synthesising findings from recent studies on macrophage polarisation and reprogramming in tumour biology.
Not applicable (review of existing literature).
DATA COLLECTION AND/OR ANALYSIS: Key studies were identified and summarised to explore mechanisms of macrophage polarisation and reprogramming, focusing on M1/M2 polarisation, metabolic and epigenetic changes, and pathway regulation.
Macrophage reprogramming in the tumour microenvironment involves complex mechanisms, including phenotypic and functional alterations. These processes are influenced by M1/M2 polarisation, metabolic and epigenetic reprogramming, and various signalling pathways. TAMs play a pivotal role in tumour progression, metastasis, and therapy resistance, making them prime targets for combination therapies.
Understanding the mechanisms underlying macrophage polarisation and reprogramming offers promising avenues for developing therapies to counteract tumour progression. Future research should focus on translating these insights into clinical applications for effective cancer treatment.
巨噬细胞是先天性免疫系统的关键组成部分,源自单核细胞,在抗炎和抗肿瘤活动中发挥重要作用。然而,在肿瘤微环境中,巨噬细胞常被重编程为肿瘤相关巨噬细胞(TAM),后者促进肿瘤生长、转移和治疗抵抗。
综述巨噬细胞极化和重编程认识方面的最新进展,强调其在肿瘤进展中的作用及作为治疗靶点的潜力。
这是一篇综述文章,综合了肿瘤生物学中巨噬细胞极化和重编程的最新研究结果。
不适用(对现有文献的综述)。
数据收集和/或分析:确定并总结关键研究,以探索巨噬细胞极化和重编程的机制,重点关注M1/M2极化、代谢和表观遗传变化以及信号通路调节。
肿瘤微环境中的巨噬细胞重编程涉及复杂机制,包括表型和功能改变。这些过程受M1/M2极化、代谢和表观遗传重编程以及各种信号通路影响。TAM在肿瘤进展、转移和治疗抵抗中起关键作用,使其成为联合治疗的主要靶点。
了解巨噬细胞极化和重编程的潜在机制为开发对抗肿瘤进展的疗法提供了有前景的途径。未来研究应专注于将这些见解转化为有效的癌症治疗临床应用。