CSF1R-Expressing Tumor-Associated Macrophages, Smoking and Survival in Lung Adenocarcinoma: Analyses Using Quantitative Phosphor-Integrated Dot Staining

被引:23
作者
Inamura, Kentaro [1 ]
Shigematsu, Yasuyuki [1 ]
Ninomiya, Hironori [1 ]
Nakashima, Yasuhiro [1 ]
Kobayashi, Maki [1 ]
Saito, Haruyuki [3 ]
Takahashi, Katsuhiro [3 ]
Futaya, Etsuko [3 ]
Okumura, Sakae [2 ]
Ishikawa, Yuichi [1 ]
Kanda, Hiroaki [1 ,4 ]
机构
[1] Japanese Fdn Canc Res, Canc Inst Hosp, Canc Inst, Dept Pathol,Koto Ku, 3-8-31 Ariake, Tokyo 1358550, Japan
[2] Japanese Fdn Canc Res, Canc Inst Hosp, Dept Thorac Surg Oncol, Koto Ku, 3-8-31 Ariake, Tokyo 1358550, Japan
[3] Konica Minolta Inc, Corp R&D Headquarters, Bio Adv Technol Div, 1 Sakura Machi, Hino, Tokyo 1918511, Japan
[4] Saitama Canc Ctr, Dept Pathol, 780 Komuro, Ina, Saitama 3620806, Japan
关键词
CSF1R; tumor-associated macrophage (TAM); phosphor-integrated dot (PID); tobacco; non-small-cell lung cancer (NSCLC); immunohistochemistry; neoantigens; tumor mutational burden; immune checkpoint inhibitor; CD163; CANCER; EXPRESSION; ANTIBODY; GENE; MICROENVIRONMENT; POLYMORPHISM; LANDSCAPE; PROGNOSIS; CELLS;
D O I
10.3390/cancers10080252
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CSF1R-expressing tumor-associated macrophages (TAMs) induce a tumor-promoting microenvironment by regulating immunity. Evidence demonstrates that the expression and single nucleotide polymorphisms of CSF1R relate with survival and risk of lung cancer in never smokers. However, no previous studies have examined the association of CSF1R expression in TAMs with mortality or whether the prognostic association differs according to smoking status in lung adenocarcinoma. Quantitative phosphor-integrated dot staining was used to precisely assess CSF1R expression in TAMs. Using 195 consecutive cases of lung adenocarcinoma, we examined the association of CSF1R expression with mortality and whether the prognostic association differs according to smoking status. We observed high expression levels of CSF1R in TAMs in 65 of 195 (33%) cases of lung adenocarcinoma. High expression levels of CSF1R were associated with high lung cancer-specific mortality (log-rank p = 0.037; hazard ratio (HR) = 1.61, 95% confidence interval (CI) = 1.02 -2.52, p = 0.043). This prognostic association differed according to smoking status (p for interaction = 0.049, between never-smoking and ever-smoking patients). The association between high expression levels of CSF1R and lung cancer-specific mortality was stronger in never-smoking patients (log-rank p = 0.0027; HR = 2.90, 95% CI = 1.41-6.11, p = 0.0041) than in ever-smoking patients (log-rank p = 0.73; HR = 1.11, 95% CI = 0.59-2.00, p = 0.73). The findings suggest that CSF1R-expressing TAMs may exert stronger tumor-promoting immunity in never-smoking patients with lung adenocarcinoma and serve as a therapeutic target in precision immunotherapies.
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页数:15
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