Cancer-promoting mechanisms of tumor-associated neutrophils

静脉注射 医学 肿瘤微环境 肿瘤进展 癌症研究 血管生成 癌症 下调和上调 免疫监视 外渗 免疫学 免疫系统 趋化因子 转移 生物 内科学 基因 生物化学
作者
Brian Hurt,Richard D. Schulick,Barish H. Edil,Karim C. El Kasmi,Carlton C. Barnett
出处
期刊:American Journal of Surgery [Elsevier]
卷期号:214 (5): 938-944 被引量:94
标识
DOI:10.1016/j.amjsurg.2017.08.003
摘要

Neutrophils have classically been considered to mount a defensive response against tumor cells, yet recent evidence suggests tumors modulate neutrophil function to support tumor growth and progression.Tumor-associated neutrophils (TANs) are phenotypically distinct from circulating neutrophils in terms of their surface protein composition and cyto/chemokine activity and response. Although TANs have been shown to both promote and inhibit tumor advancement, the preponderant activity augments tumor progression. This review discusses these cancer-promoting molecular pathways, relevant diagnostic studies in patients, and subsequent treatment modalities. The tumor promoting mechanisms of TANs include dampening of CD8+ response via Arginase-1; a neutrophil-secreted neutrophil elastase (NE) upregulation of tumor cellular proliferation pathways; degradation of basement membrane and ECM via NE and MMP-9; upregulation of angiogenesis by VEGF, and HGF; and ICAM-1 dependent tumor intravasation, immune protection in circulation, and extravasation into distant, metastatic tissue beds. Clinicians are constrained in treating TANs systemically as it may induce neutropenia, therefore targeting TANs-mediated tumor progression pathways surgically on a loco-regional level is a viable adjuvant treatment modality.TANs modulate the tumor microenvironment promoting tumor progression. Mechanistic understanding of TANs role in tumor progression will provide unique therapeutic alternatives.
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