Clinicopathological significance of peritumoral alveolar macrophages in patients with resected early-stage lung squamous cell carcinoma

被引:6
|
作者
Tanaka, Yu [1 ,2 ,3 ,4 ]
Nakai, Tokiko [1 ,2 ]
Suzuki, Ayako [5 ]
Kagawa, Yosuke [1 ,2 ,3 ]
Noritake, Osamu [1 ,2 ,6 ]
Taki, Tetsuro [1 ,2 ]
Hashimoto, Hiroko [7 ,8 ]
Sakai, Tetsuya [3 ]
Shibata, Yuji [3 ]
Izumi, Hiroki [3 ]
Nosaki, Kaname [3 ]
Udagawa, Hibiki [3 ]
Zenke, Yoshitaka [3 ]
Matsumoto, Shingo [3 ]
Yoh, Kiyotaka [3 ]
Miyazaki, Saori [1 ,2 ]
Sakamoto, Naoya [1 ,2 ,9 ]
Sakashita, Shingo [1 ,2 ,9 ]
Kojima, Motohiro [1 ,2 ,9 ]
Watanbe, Reiko [1 ,2 ]
Tsuboi, Masahiro [6 ]
Goto, Koichi [3 ]
Ishii, Genichiro [1 ,2 ,4 ,7 ,8 ]
机构
[1] Natl Canc Ctr Hosp East, Dept Pathol, Kashiwa, Chiba, Japan
[2] Natl Canc Ctr Hosp East, Clin Labs, Kashiwa, Chiba, Japan
[3] Natl Canc Ctr Hosp East, Dept Thorac Oncol, Kashiwa, Chiba, Japan
[4] Juntendo Univ, Course Adv Clin Res Canc, Grad Sch Med, Tokyo, Japan
[5] Univ Tokyo, Dept Computat Biol & Med Sci, Kashiwa, Chiba, Japan
[6] Natl Canc Ctr Hosp East, Dept Thorac Surg, Kashiwa, Chiba, Japan
[7] Natl Canc Ctr, Exploratory Oncol Res & Clin Trial Ctr, Div Innovat Pathol, Kashiwa, Chiba, Japan
[8] Natl Canc Ctr, Exploratory Oncol Res & Clin Trial Ctr, Lab Med, Kashiwa, Chiba, Japan
[9] Clin Trial Ctr, Natl Canc Ctr, Div Pathol, Exploratory Oncol Res & Clin Trial Ctr, Kashiwa, Chiba, Japan
关键词
Peritumoral immune microenvironment; Alveolar macrophages; Lung squamous cell carcinoma; Ex vivo BALF; CCL2; TUMOR-ASSOCIATED MACROPHAGES; CANCER;
D O I
10.1007/s00262-023-03393-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction This study aimed to clarify the correlation between the number of AMs and prognosis and to examine the gene expression of AMs in lung squamous cell carcinoma (SqCC). Methods We reviewed 124 stage I lung SqCC cases in our hospital and 139 stage I lung SqCC cases in The Cancer Genome Atlas (TCGA) cohort in this study. We counted the number of AMs in the peritumoral lung field (P-AMs) and in the lung field distant from the tumor (D-AMs). Moreover, we performed a novel ex vivo bronchoalveolar lavage fluid (BALF) analysis to select AMs from surgically resected lung SqCC cases and examined the expression of IL10, CCL2, IL6, TGF beta, and TNF alpha (n = 3). Results Patients with high P-AMs had significantly shorter overall survival (OS) (p < 0.01); however, patients with high D-AMs did not have significantly shorter OS. Moreover, in TCGA cohort, patients with high P-AMs had a significantly shorter OS (p < 0.01). In multivariate analysis, a higher number of P-AMs were an independent poor prognostic factor (p = 0.02). Ex vivo BALF analysis revealed that AMs collected from the tumor vicinity showed higher expression of IL10 and CCL2 than AMs from distant lung fields in all 3 cases (IL-10: 2.2-, 3.0-, and 10.0-fold; CCL-2: 3.0-, 3.1-, and 3.2-fold). Moreover, the addition of recombinant CCL2 significantly increased the proliferation of RERF-LC-AI, a lung SqCC cell line. Conclusion The current results indicated the prognostic impact of the number of peritumoral AMs and suggested the importance of the peritumoral tumor microenvironment in lung SqCC progression.
引用
收藏
页码:2205 / 2215
页数:11
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