Prognostic value of diametrically polarized tumor- associated macrophages in multiple myeloma

被引:46
作者
Chen, Xinyi [1 ]
Chen, Jin [2 ]
Zhang, Wenyan [3 ]
Sun, Ruixue [1 ]
Liu, Ting [1 ]
Zheng, Yuhuan [1 ]
Wu, Yu [1 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Hematol, Hematol Res Lab, Chengdu, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Dept Rheumatol & Immunol, Chengdu, Sichuan, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Pathol, Chengdu, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
multiple myeloma; tumor-associated macrophages; overall response; prognosis; nomogram; IMMUNE CONTEXTURE; CANCER; ACTIVATION; SURVIVAL; THERAPY; PARADIGM; SUBSETS; DISEASE; IMPACT;
D O I
10.18632/oncotarget.22340
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumor-associated macrophages (TAMs) are correlated with the prognosis of different types of solid tumors and lymphoma, according to many clinical studies. In vitro experiments have demonstrated the roles of these cells in myeloma cell survival, angiogenesis, immunomodulation, drug resistance, and the interaction between malignant myeloma cells and the microenvironment. Here, we investigated the prognostic significance of TAMs in patients with multiple myeloma (MM). We evaluated the polarized functional status of bone marrow infiltrated by TAMs by immunohistochemical staining of CD68, iNOS, and CD163 in 240 patients with MM from January 2009 to December 2014. The overall response rates to chemotherapy were lower in patients with high CD68+ or CD163+ TAM densities than in those with low densities. Kaplan-Meier analysis showed that the progression-free survival (PFS, p = 0.001) and overall survival (OS, p < 0.001) of patients with low CD163+ TAM density were significantly higher than those of patients with high CD163+ TAM density. Furthermore, combined analysis of iNOS+ and CD163+ TAMs (iNOS/CD163 signature) exhibited greater power in predicting patient outcomes for both PFS (p < 0.001) and OS (p < 0.001). Moreover, Cox regression analysis identified iNOS+ and CD163+ TAMs as independent prognostic factors (p = 0.007, p < 0.001, respectively). These factors could be combined with the international staging system (ISS) to generate a predictive nomogram for patient outcomes. Our findings suggest that the mosaic of diametrically polarized TAMs is a novel independent prognostic factor that could be integrated into the evaluation of and therapy for MM.
引用
收藏
页码:112685 / 112696
页数:12
相关论文
共 37 条
[1]   Monocyte/macrophage-derived soluble CD163: a novel biomarker in multiple myeloma [J].
Andersen, Morten N. ;
Abildgaard, Niels ;
Maniecki, Maciej B. ;
Moller, Holger J. ;
Andersen, Niels F. .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2014, 93 (01) :41-47
[2]   Smoldering and polarized inflammation in the initiation and promotion of malignant disease [J].
Balkwill, F ;
Charles, KA ;
Mantovani, A .
CANCER CELL, 2005, 7 (03) :211-217
[3]   Macrophage plasticity and interaction with lymphocyte subsets: cancer as a paradigm [J].
Biswas, Subhra K. ;
Mantovani, Alberto .
NATURE IMMUNOLOGY, 2010, 11 (10) :889-896
[4]   IMWG consensus on risk stratification in multiple myeloma [J].
Chng, W. J. ;
Dispenzieri, A. ;
Chim, C-S ;
Fonseca, R. ;
Goldschmidt, H. ;
Lentzsch, S. ;
Munshi, N. ;
Palumbo, A. ;
Miguel, J. S. ;
Sonneveld, P. ;
Cavo, M. ;
Usmani, S. ;
Durie, B. G. M. ;
Avet-Loiseau, H. .
LEUKEMIA, 2014, 28 (02) :269-277
[5]   Macrophage Regulation of Tumor Responses to Anticancer Therapies [J].
De Palma, Michele ;
Lewis, Claire E. .
CANCER CELL, 2013, 23 (03) :277-286
[6]   Interferon-γ reverses the immunosuppressive and protumoral properties and prevents the generation of human tumor-associated macrophages [J].
Duluc, Dorothee ;
Corvaisier, Murielle ;
Blanchard, Simon ;
Catala, Laurent ;
Descamps, Philippe ;
Gamelin, Erick ;
Ponsoda, Stephane ;
Delneste, Yves ;
Hebbar, Mohamed ;
Jeannin, Pascale .
INTERNATIONAL JOURNAL OF CANCER, 2009, 125 (02) :367-373
[7]  
Dupont, 2020, HMISC HARRELL MISCEL
[8]   International uniform response criteria for multiple myeloma [J].
Durie, B. G. M. ;
Harousseau, J-L ;
Miguel, J. S. ;
Blade, J. ;
Barlogie, B. ;
Anderson, K. ;
Gertz, M. ;
Dimopoulos, M. ;
Westin, J. ;
Sonneveld, P. ;
Ludwig, H. ;
Gahrton, G. ;
Beksac, M. ;
Crowley, J. ;
Belch, A. ;
Boccadaro, M. ;
Turesson, I. ;
Joshua, D. ;
Vesole, D. ;
Kyle, R. ;
Alexanian, R. ;
Tricot, G. ;
Attal, M. ;
Merlini, G. ;
Powles, R. ;
Richardson, P. ;
Shimizu, K. ;
Tosi, P. ;
Morgan, G. ;
Rajkumar, S. V. .
LEUKEMIA, 2006, 20 (09) :1467-1473
[9]   An antiinflammatory role for IKKβ through the inhibition of "classical" macrophage activation [J].
Fong, Carol Ho Yan ;
Bebien, Magali ;
Didierlaurent, Arnaud ;
Nebauer, Ruth ;
Hussell, Tracy ;
Broide, David ;
Karin, Michael ;
Lawrence, Toby .
JOURNAL OF EXPERIMENTAL MEDICINE, 2008, 205 (06) :1269-1276
[10]   The immune contexture in human tumours: impact on clinical outcome [J].
Fridman, Wolf Herman ;
Pages, Franck ;
Sautes-Fridman, Catherine ;
Galon, Jerome .
NATURE REVIEWS CANCER, 2012, 12 (04) :298-306