Inhibition of Colony-Stimulating Factor-1 Receptor Enhances the Efficacy of Radiotherapy and Reduces Immune Suppression in Glioblastoma

被引:34
作者
Almahariq, Muayad F. [1 ]
Quinn, Thomas J. [1 ]
Kesarwani, Pravin [1 ]
Kant, Shiva [1 ]
Miller, C. Ryan [2 ]
Chinnaiyan, Prakash [1 ,3 ]
机构
[1] Beaumont Hlth, Dept Radiat Oncol, Royal Oak, MI 48073 USA
[2] Univ Alabama Birmingham, ONeal Comprehens Canc Ctr, Comprehens Neurosci Ctr, Div Neuropathol,Dept Pathol,Sch Med, Birmingham, AL 35294 USA
[3] Oakland Univ, William Beaumont Sch Med, Rochester, MI 48063 USA
来源
IN VIVO | 2021年 / 35卷 / 01期
关键词
Glioblastoma; CSF-1R; M2; macrophages; immunosuppression; RECURRENT GLIOBLASTOMA; RADIATION; TUMORS; POLARIZATION; SURVIVAL; CELLS; PI3K; MACROPHAGES; COMBINATION; THERAPY;
D O I
10.21873/invivo.12239
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Aim: To use inhibition of colony-stimulating factor-1 receptor (CSF-IR) to target tumor-associated macrophages (TAMs) and improve the efficacy of radiotherapy in glioblastoma (GBM). Materials and Methods: The CSF-IR inhibitor BLZ-945 was used to examine the impact of CSF-IR inhibition on M2 polarization in vitro. Using an orthotopic, immunocompetent GBM model, mice were treated with vehicle, RT, BLZ-945, or RT plus BLZ-945. Results: BLZ-945 reduced M2 polarization in vitro. BLZ-945 alone did not improve median overall survival (mOS=29 days) compared to control mice (mOS=27 days). RT improved survival (mOS=45 days; p=0.02), while RT plus BLZ-945 led to the longest survival (mOS=not reached; p=0.005). Resected tumors had a relatively large population of M2 TAMs in GBM at baseline, which was increased in response to RT. BLZ-945 reduced RT-induced M2 infiltration. Conclusion: Inhibition of CSF-IR improved response to RT in the treatment of GBM and may represent a promising strategy to improve RT-induced antitumor immune responses.
引用
收藏
页码:119 / 129
页数:11
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