Prognostic Impact of CD204-Positive Macrophages in Lung Squamous Cell Carcinoma Possible Contribution of Cd204-Positive Macrophages to the Tumor-Promoting Microenvironment

被引:84
作者
Hirayama, Shunki [2 ,3 ]
Ishii, Genichiro [1 ]
Nagai, Kanji [2 ]
Ono, Shotaro [3 ]
Kojima, Motohiro
Yamauchi, Chisako
Aokage, Keiju [2 ]
Hishida, Tomoyuki [2 ]
Yoshida, Junji [2 ]
Suzuki, Kenji [3 ]
Ochiai, Atsushi
机构
[1] Natl Canc Ctr Hosp E, Div Pathol, Res Ctr Innovat Oncol, Dept Pathol, Kashiwa, Chiba 2778577, Japan
[2] Natl Canc Ctr Hosp E, Dept Thorac Oncol, Res Ctr Innovat Oncol, Kashiwa, Chiba 2778577, Japan
[3] Juntendo Univ, Sch Med, Dept Gen Thorac Surg, Tokyo 113, Japan
基金
日本学术振兴会;
关键词
CD204; Tumor associated macrophages; Non-small-cell lung carcinoma; Squamous cell carcinoma; TUMOR-ASSOCIATED MACROPHAGES; MAMMARY-TUMORS; BREAST-CANCER; T-CELLS; PROGRESSION; ANGIOGENESIS; INFILTRATION; INFLAMMATION; METASTASIS; RECURRENCE;
D O I
10.1097/JTO.0b013e3182745968
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Introduction: Tumor-associated macrophages (TAMs) are recruited into cancer-induced stroma and produce a specific microenvironment for cancer progression. CD204 (+) TAMs are reportedly related to tumor progression and clinical outcome in some tumors. The aim of this study was to clarify the correlation between CD204 (+) TAMs and the clinicopathological features of lung squamous cell carcinoma. Methods: We investigated the relationships between the numbers of CD204 (+) TAMs and clinicopathological factors, microvessel density, and the numbers of Foxp3 (+) lymphocytes in 208 consecutively resected cases. We also examined the relationships between the numbers of CD204 (+) TAMs and the expression levels of cytokines involved in the migration and differentiation of CD204 (+) TAMs. Results: A high number of CD204 (+) TAMs in the stroma was significantly correlated with an advanced p-stage, T factor, N factor, and the presence of vascular and pleural invasion. A high number of CD204 (+) TAMs in the stroma was also a significant prognostic factor for all p-stages and p-stage I. Moreover, the numbers of CD204 (+) TAMs were correlated with the microvessel density and the numbers of Foxp3 (+) lymphocytes. A high number of CD204 (+) TAMs was strongly correlated with the tissue expression level of monocyte chemoattractant protein-1. CD204 (+) TAMs were shown to be significant independent prognostic factors in a multivariate analysis. Conclusions: CD204 (+) TAMs were an independent prognostic factor in lung squamous cell carcinoma. CD204 (+) TAMs, along with other tumor-promoting stromal cells such as regulatory T cells and endothelial cells, may create tumor-promoting microenvironments.
引用
收藏
页码:1790 / 1797
页数:8
相关论文
共 26 条
[1]
The inflammatory micro-environment in tumor progression: The role of tumor-associated macrophages [J].
Allavena, Paola ;
Sica, Antonio ;
Solinas, Graziella ;
Porta, Chiara ;
Mantovani, Alberto .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2008, 66 (01) :1-9
[2]
Scavenger receptor-A-targeted leukocyte depletion inhibits peritoneal ovarian tumor progression [J].
Bak, S. Peter ;
Walters, Julie Jo ;
Takeya, Motohiro ;
Conejo-Garcia, Jose R. ;
Berwin, Brent L. .
CANCER RESEARCH, 2007, 67 (10) :4783-4789
[3]
Inflammation and cancer: back to Virchow? [J].
Balkwill, F ;
Mantovani, A .
LANCET, 2001, 357 (9255) :539-545
[4]
The role of tumour-associated macrophages in tumour progression: implications for new anticancer therapies [J].
Bingle, L ;
Brown, NJ ;
Lewis, CE .
JOURNAL OF PATHOLOGY, 2002, 196 (03) :254-265
[5]
Stromal MCP-1 in mammary tumors induces tumor-associated macrophage infiltration and contributes to tumor progression [J].
Fujimoto, Hiroshi ;
Sangai, Takafumi ;
Ishii, Genichiro ;
Ikehara, Akashi ;
Nagashima, Takeshi ;
Miyazaki, Masaru ;
Ochiai, Atsushi .
INTERNATIONAL JOURNAL OF CANCER, 2009, 125 (06) :1276-1284
[6]
Corosolic acid inhibits glioblastoma cell proliferation by suppressing the activation of signal transducer and activator of transcription-3 and nuclear factor-kappa B in tumor cells and tumor-associated macrophages [J].
Fujiwara, Yukio ;
Komohara, Yoshihiro ;
Ikeda, Tsuyoshi ;
Takeya, Motohiro .
CANCER SCIENCE, 2011, 102 (01) :206-211
[7]
An amino-bisphosphonate targets MMP-9-expressing macrophages and angiogenesis to impair cervical carcinogenesis [J].
Giraudo, E ;
Inoue, M ;
Hanahan, D .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (05) :623-633
[8]
Enhanced invasiveness of breast cancer cell lines upon co-cultivation with macrophages is due to TNF-α dependent up-regulation of matrix metalloproteases [J].
Hagemann, T ;
Robinson, SC ;
Schulz, M ;
Trümper, L ;
Balkwill, FR ;
Binder, C .
CARCINOGENESIS, 2004, 25 (08) :1543-1549
[9]
Ovarian cancer cells polarize macrophages toward a tumor-associated phenotype [J].
Hagemann, Thorsten ;
Wilson, Julia ;
Burke, Frances ;
Kulbe, Hagen ;
Li, Ninfeng Fiona ;
Pluddemann, Annette ;
Charles, Kellie ;
Gordon, Siamon ;
Balkwill, Frances R. .
JOURNAL OF IMMUNOLOGY, 2006, 176 (08) :5023-5032
[10]
Significance of alternatively activated macrophages in patients with intrahepatic cholangiocarcinoma [J].
Hasita, Horlad ;
Komohara, Yoshihiro ;
Okabe, Hirohisa ;
Masuda, Toshiro ;
Ohnishi, Koji ;
Lei, Xiao F. ;
Beppu, Toru ;
Baba, Hideo ;
Takeya, Motohiro .
CANCER SCIENCE, 2010, 101 (08) :1913-1919