Macrophage Regulation of Tumor Responses to Anticancer Therapies

被引:929
作者
De Palma, Michele [1 ]
Lewis, Claire E. [2 ]
机构
[1] Swiss Fed Inst Technol Lausanne EPFL, Swiss Inst Expt Canc Res ISREC, Sch Life Sci, CH-1015 Lausanne, Switzerland
[2] Univ Sheffield, Sch Med, Dept Oncol, Sheffield Canc Res Ctr, Sheffield S10 2RX, S Yorkshire, England
基金
欧洲研究理事会;
关键词
ENDOTHELIAL GROWTH-FACTOR; MYELOID CELLS; INFILTRATING MACROPHAGES; SUPPRESSOR-CELLS; ANGIOGENESIS; CANCER; POLARIZATION; PROGRESSION; MONOCYTES; PLASTICITY;
D O I
10.1016/j.ccr.2013.02.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumor-associated macrophages (TAMs) promote key processes in tumor progression, like angiogenesis, immunosuppression, invasion, and metastasis. Increasing studies have also shown that TAMs can either enhance or antagonize the antitumor efficacy of cytotoxic chemotherapy, cancer-cell targeting antibodies, and immunotherapeutic agents depending on the type of treatment and tumor model. TAMs also drive reparative mechanisms in tumors after radiotherapy or treatment with vascular-targeting agents. Here, we discuss the biological significance and clinical implications of these findings, with an emphasis on novel approaches that effectively target TAMs to increase the efficacy of such therapies.
引用
收藏
页码:277 / 286
页数:10
相关论文
共 88 条
[1]   Inhibition of Mac-1 (CD11b/CD18) enhances tumor response to radiation by reducing myeloid cell recruitment [J].
Ahn, G-One ;
Tseng, Diane ;
Liao, Cho-Hwa ;
Dorie, Mary Jo ;
Czechowicz, Agnieszka ;
Brown, J. Martin .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (18) :8363-8368
[2]   FcRγ Activation Regulates Inflammation-Associated Squamous Carcinogenesis [J].
Andreu, Pauline ;
Johansson, Magnus ;
Affara, Nesrine I. ;
Pucci, Ferdinando ;
Tan, Tingting ;
Junankar, Simon ;
Korets, Lidiya ;
Lam, Julia ;
Tawfik, David ;
DeNardo, David G. ;
Naldini, Luigi ;
de Visser, Karin E. ;
De Palma, Michele ;
Coussens, Lisa M. .
CANCER CELL, 2010, 17 (02) :121-134
[3]   Migration of human monocytes in response to vascular endothelial growth factor (VEGF) is mediated via the VEGF receptor flt-1 [J].
Barleon, B ;
Sozzani, S ;
Zhou, D ;
Weich, HA ;
Mantovani, A ;
Marme, D .
BLOOD, 1996, 87 (08) :3336-3343
[4]   CD40 Agonists Alter Tumor Stroma and Show Efficacy Against Pancreatic Carcinoma in Mice and Humans [J].
Beatty, Gregory L. ;
Chiorean, Elena G. ;
Fishman, Matthew P. ;
Saboury, Babak ;
Teitelbaum, Ursina R. ;
Sun, Weijing ;
Huhn, Richard D. ;
Song, Wenru ;
Li, Dongguang ;
Sharp, Leslie L. ;
Torigian, Drew A. ;
O'Dwyer, Peter J. ;
Vonderheide, Robert H. .
SCIENCE, 2011, 331 (6024) :1612-1616
[5]   Modes of resistance to anti-angiogenic therapy [J].
Bergers, Gabriele ;
Hanahan, Douglas .
NATURE REVIEWS CANCER, 2008, 8 (08) :592-603
[6]   Macrophages promote angiogenesis in human breast tumour spheroids in vivo [J].
Bingle, L ;
Lewis, CE ;
Corke, KP ;
Reed, MWR ;
Brown, NJ .
BRITISH JOURNAL OF CANCER, 2006, 94 (01) :101-107
[7]   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
[8]   Macrophage plasticity and interaction with lymphocyte subsets: cancer as a paradigm [J].
Biswas, Subhra K. ;
Mantovani, Alberto .
NATURE IMMUNOLOGY, 2010, 11 (10) :889-896
[9]   Chemotherapy-triggered cathepsin B release in myeloid-derived suppressor cells activates the Nlrp3 inflammasome and promotes tumor growth [J].
Bruchard, Melanie ;
Mignot, Gregoire ;
Derangere, Valentin ;
Chalmin, Fanny ;
Chevriaux, Angelique ;
Vegran, Frederique ;
Boireau, Wilfrid ;
Simon, Benoit ;
Ryffel, Bernhard ;
Connat, Jean Louis ;
Kanellopoulos, Jean ;
Martin, Francois ;
Rebe, Cedric ;
Apetoh, Lionel ;
Ghiringhelli, Francois .
NATURE MEDICINE, 2013, 19 (01) :57-64
[10]  
Cai Z., 2013, CANC RES