医学
癌症研究
癌症
免疫疗法
前列腺癌
血管生成
结直肠癌
转移
巨噬细胞
肿瘤科
内科学
生物
体外
生物化学
作者
Enar Jumaniyazova,А. V. Lokhonina,D. Sh. Dzhalilova,Е. А. Miroshnichenko,А. М. Косырева,Timur Fatkhudinov
出处
期刊:Cancers
[Multidisciplinary Digital Publishing Institute]
日期:2025-01-21
卷期号:17 (3): 342-342
标识
DOI:10.3390/cancers17030342
摘要
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.
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