Jumaniyazova Enar, Lokhonina Anastasiya, Dzhalilova Dzhuliia, Miroshnichenko Ekaterina, Kosyreva Anna, Fatkhudinov Timur
Research Institute of Molecular and Cellular Medicine, Peoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya Street, 117198 Moscow, Russia.
Avtsyn Research Institute of Human Morphology, FSBSI Petrovsky National Research Centre of Surgery, 3 Tsyurupy Street, 117418 Moscow, Russia.
Cancers (Basel). 2025 Jan 21;17(3):342. doi: 10.3390/cancers17030342.
In solid tumors, tumor-associated macrophages (TAMs) are one of the most numerous populations and play an important role in the processes of tumor cell invasion, metastasis, and angiogenesis. Therefore, TAMs are considered promising diagnostic and prognostic biomarkers of tumors, and many attempts have been made to influence these cells as part of antitumor therapy. There are several key principles of action on ТАМs: the inhibition of monocyte/macrophage transition; the destruction of macrophages; the reprogramming of macrophage phenotypes (polarization of M2 macrophages to M1); the stimulation of phagocytic activity of macrophages and CAR-M therapy. Despite the large number of studies in this area, to date, there are no adequate approaches using antitumor therapy based on alterations in TAM functioning that would show high efficacy when administered in a mono-regimen for the treatment of malignant neoplasms. Studies devoted to the evaluation of the efficacy of drugs acting on TAMs are characterized by a small sample and the large heterogeneity of patient groups; in addition, in such studies, chemotherapy or immunotherapy is used, which significantly complicates the evaluation of the effectiveness of the agent acting on TAMs. In this review, we attempted to systematize the evidence on attempts to influence TAMs in malignancies such as lung cancer, breast cancer, colorectal cancer, cervical cancer, prostate cancer, gastric cancer, head and neck squamous cell cancer, and soft tissue sarcomas.
在实体瘤中,肿瘤相关巨噬细胞(TAMs)是数量最多的细胞群体之一,在肿瘤细胞侵袭、转移和血管生成过程中发挥重要作用。因此,TAMs被认为是有前景的肿瘤诊断和预后生物标志物,并且已经进行了许多尝试,将影响这些细胞作为抗肿瘤治疗的一部分。对TAMs的作用有几个关键原则:抑制单核细胞/巨噬细胞转变;破坏巨噬细胞;重新编程巨噬细胞表型(将M2巨噬细胞极化为M1);刺激巨噬细胞的吞噬活性以及CAR-M疗法。尽管该领域有大量研究,但迄今为止,尚无基于TAM功能改变的抗肿瘤治疗的充分方法,这些方法在单药治疗恶性肿瘤时能显示出高疗效。致力于评估作用于TAMs的药物疗效的研究,其特点是样本量小且患者群体异质性大;此外,在这类研究中使用了化疗或免疫疗法,这显著使评估作用于TAMs的药物的有效性变得复杂。在这篇综述中,我们试图系统整理关于在肺癌、乳腺癌、结直肠癌、宫颈癌、前列腺癌、胃癌、头颈部鳞状细胞癌和软组织肉瘤等恶性肿瘤中影响TAMs的尝试的证据。