静脉注射
肿瘤微环境
生物
免疫疗法
癌症研究
肿瘤进展
转移
原发性肿瘤
外渗
免疫学
巨噬细胞
血管生成
免疫系统
先天免疫系统
癌症
体外
生物化学
遗传学
作者
Roy Noy,Jeffrey W. Pollard
出处
期刊:Immunity
[Elsevier]
日期:2014-07-01
卷期号:41 (1): 49-61
被引量:3255
标识
DOI:10.1016/j.immuni.2014.06.010
摘要
The tumor microenvironment is a complex ecology of cells that evolves with and provides support to tumor cells during the transition to malignancy. Among the innate and adaptive immune cells recruited to the tumor site, macrophages are particularly abundant and are present at all stages of tumor progression. Clinical studies and experimental mouse models indicate that these macrophages generally play a protumoral role. In the primary tumor, macrophages can stimulate angiogenesis and enhance tumor cell invasion, motility, and intravasation. During monocytes and/or metastasis, macrophages prime the premetastatic site and promote tumor cell extravasation, survival, and persistent growth. Macrophages are also immunosuppressive, preventing tumor cell attack by natural killer and T cells during tumor progression and after recovery from chemo- or immunotherapy. Therapeutic success in targeting these protumoral roles in preclinical models and in early clinical trials suggests that macrophages are attractive targets as part of combination therapy in cancer treatment.
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