Genitourinary Program, Roswell Park Cancer Institute, Buffalo, NY, USA.
Department of Medicine, Indiana University-Simon Cancer Center, Indianapolis, IN, USA.
Oncoimmunology. 2018 May 7;8(10):e1072672. doi: 10.1080/2162402X.2015.1072672. eCollection 2019.
Infiltrating myeloid derived suppressor cells and tumor-associated macrophages (TAMs) are important components of the immunosuppressive tumor microenvironment. We recently reported that tasquinimod, which binds to S100A9, impairs both infiltration and function of these cells. Here we discuss the underlying mechanisms responsible for targeting multiple suppressive populations and the modulation of the tumor microenvironment.
浸润性髓系来源的抑制性细胞和肿瘤相关巨噬细胞(TAMs)是免疫抑制性肿瘤微环境的重要组成部分。我们最近报道称,tasquinimod 与 S100A9 结合,可损害这些细胞的浸润和功能。在这里,我们讨论了靶向多种抑制性群体的潜在机制以及肿瘤微环境的调节。