Department of Surgery, University of California, San Francisco, Box 1710 UCSF, San Francisco, CA 94143-1710, USA.
Expert Rev Mol Diagn. 2011 Jan;11(1):91-100. doi: 10.1586/erm.10.97.
While several inflammatory cell types participate in cancer development, macrophages specifically play a key role in breast cancer, where they appear to be part of the pathogenesis of high-grade tumors. Tumor-associated macrophages (TAMs) produce factors that promote angiogenesis, remodel tissue and dampen the immune response to tumors. Specific macrophage types contribute to increased metastases in animal models, while human studies show an association between TAMs and tumors with poor prognostic features. Macrophages display a spectrum of phenotypic states, with the tumor microenvironment skewing TAMs towards a 'nonclassical' activation state, known as the M2, or wound healing/regulatory state. These TAMs are found in high-risk breast cancers, making them an important therapeutic target to explore. Improved techniques for identifying TAMs should translate into clinical applications for prognosis and treatment.
虽然有几种炎症细胞类型参与癌症的发展,但巨噬细胞在乳腺癌中特别起着关键作用,它们似乎是高级别肿瘤发病机制的一部分。肿瘤相关巨噬细胞(TAMs)产生促进血管生成、重塑组织和抑制肿瘤免疫反应的因子。特定的巨噬细胞类型有助于增加动物模型中的转移,而人类研究表明 TAMs 与预后不良特征的肿瘤之间存在关联。巨噬细胞表现出一系列表型状态,肿瘤微环境使 TAMs 向“非经典”激活状态倾斜,即 M2 或伤口愈合/调节状态。这些 TAMs 存在于高风险的乳腺癌中,使它们成为一个重要的治疗靶点。用于识别 TAMs 的改进技术应该转化为用于预后和治疗的临床应用。