Tumor-Associated Macrophages in Gliomas-Basic Insights and Treatment Opportunities

被引:63
作者
Andersen, Johannes K. [1 ]
Miletic, Hrvoje [1 ,2 ]
Hossain, Jubayer A. [1 ]
机构
[1] Univ Bergen, Dept Biomed, N-5009 Bergen, Norway
[2] Haukeland Hosp, Dept Pathol, N-5009 Bergen, Norway
关键词
glioma; glioblastoma; immunotherapy; macrophage; microglia; tumor-associated macrophages (TAMs); targeted therapies; TAM biomarker; immune checkpoints; CENTRAL-NERVOUS-SYSTEM; TOLL-LIKE RECEPTORS; T-CELLS; MICROENVIRONMENTAL LANDSCAPE; ADJUVANT TEMOZOLOMIDE; THERAPEUTIC TARGET; HUMAN GLIOBLASTOMA; KEY ROLE; MICROGLIA; POLARIZATION;
D O I
10.3390/cancers14051319
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Glioma refers to a group of primary brain tumors which includes glioblastoma (GBM), astrocytoma and oligodendroglioma as major entities. Among these, GBM is the most frequent and most malignant one. The highly infiltrative nature of gliomas, and their intrinsic intra- and intertumoral heterogeneity, pose challenges towards developing effective treatments. The glioma microenvironment, in addition, is also thought to play a critical role during tumor development and treatment course. Unlike most other solid tumors, the glioma microenvironment is dominated by macrophages and microglia-collectively known as tumor-associated macrophages (TAMs). TAMs, like their homeostatic counterparts, are plastic in nature and can polarize to either pro-inflammatory or immunosuppressive states. Many lines of evidence suggest that immunosuppressive TAMs dominate the glioma microenvironment, which fosters tumor development, contributes to tumor aggressiveness and recurrence and, very importantly, impedes the therapeutic effect of various treatment regimens. However, through the development of new therapeutic strategies, TAMs can potentially be shifted towards a proinflammatory state which is of great therapeutic interest. In this review, we will discuss various aspects of TAMs in the context of glioma. The focus will be on the basic biology of TAMs in the central nervous system (CNS), potential biomarkers, critical evaluation of model systems for studying TAMs and finally, special attention will be given to the potential targeted therapeutic options that involve the TAM compartment in gliomas.
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页数:25
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共 203 条
[1]
CD47 Blockade by Hu5F9-G4 and Rituximab in Non-Hodgkin's Lymphoma [J].
Advani, Ranjana ;
Flinn, Ian ;
Popplewell, Leslie ;
Forero, Andres ;
Bartlett, Nancy L. ;
Ghosh, Nilanjan ;
Kline, Justin ;
Roschewski, Mark ;
LaCasce, Ann ;
Collins, Graham P. ;
Thu Tran ;
Lynn, Judith ;
Chen, James Y. ;
Volkmer, Jens-Peter ;
Agoram, Balaji ;
Huang, Jie ;
Majeti, Ravindra ;
Weissman, Irving L. ;
Takimoto, Chris H. ;
Chao, Mark P. ;
Smith, Sonali M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2018, 379 (18) :1711-1721
[2]
Toll-like receptor signalling [J].
Akira, S ;
Takeda, K .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (07) :499-511
[3]
Dynamic changes in glioma macrophage populations after radiotherapy reveal CSF-1R inhibition as a strategy to overcome resistance [J].
Akkari, Leila ;
Bowman, Robert L. ;
Tessier, Jeremy ;
Klemm, Florian ;
Handgraaf, Shanna M. ;
de Groot, Marnix ;
Quail, Daniela F. ;
Tillard, Lucie ;
Gadiot, Jules ;
Huse, Jason T. ;
Brandsma, Dieta ;
Westerga, Johan ;
Watts, Colin ;
Joyce, Johanna A. .
SCIENCE TRANSLATIONAL MEDICINE, 2020, 12 (552)
[4]
Pre-clinical tumor models of primary brain tumors: Challenges and opportunities [J].
Akter, Farhana ;
Simon, Brennan ;
de Boer, Nadine Leonie ;
Redjal, Navid ;
Wakimoto, Hiroaki ;
Shah, Khalid .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2021, 1875 (01)
[5]
Challenges to curing primary brain tumours [J].
Aldape, Kenneth ;
Brindle, Kevin M. ;
Chesler, Louis ;
Chopra, Rajesh ;
Gajjar, Amar ;
Gilbert, Mark R. ;
Gottardo, Nicholas ;
Gutmann, David H. ;
Hargrave, Darren ;
Holland, Eric C. ;
Jones, David T. W. ;
Joyce, Johanna A. ;
Kearns, Pamela ;
Kieran, Mark W. ;
Mellinghoff, Ingo K. ;
Merchant, Melinda ;
Pfister, Stefan M. ;
Pollard, Steven M. ;
Ramaswamy, Vijay ;
Rich, Jeremy N. ;
Robinson, Giles W. ;
Rowitch, David H. ;
Sampson, John H. ;
Taylor, Michael D. ;
Workman, Paul ;
Gilbertson, Richard J. .
NATURE REVIEWS CLINICAL ONCOLOGY, 2019, 16 (08) :509-520
[6]
Adult Glioblastoma [J].
Alexander, Brian M. ;
Cloughesy, Timothy F. .
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35 (21) :2402-+
[7]
Microglia derive from progenitors, originating from the yolk sac, and which proliferate in the brain [J].
Alliot, F ;
Godin, I ;
Pessac, B .
DEVELOPMENTAL BRAIN RESEARCH, 1999, 117 (02) :145-152
[8]
White matter microglia heterogeneity in the CNS [J].
Amor, Sandra ;
McNamara, Niamh B. ;
Gerrits, Emma ;
Marzin, Manuel C. ;
Kooistra, Susanne M. ;
Miron, Veronique E. ;
Nutma, Erik .
ACTA NEUROPATHOLOGICA, 2022, 143 (02) :125-141
[9]
Glial and myeloid heterogeneity in the brain tumour microenvironment [J].
Andersen, Brian M. ;
Akl, Camilo Faust ;
Wheeler, Michael A. ;
Chiocca, E. Antonio ;
Reardon, David A. ;
Quintana, Francisco J. .
NATURE REVIEWS CANCER, 2021, 21 (12) :786-802
[10]
Switching off CD73: a way to boost the activity of conventional and targeted antineoplastic therapies [J].
Antonio, Luca ;
Novitskiy, Sergey V. ;
Sachsenmeier, Kris F. ;
Fornai, Matteo ;
Blandizzi, Corrado ;
Hasko, Gyorgy .
DRUG DISCOVERY TODAY, 2017, 22 (11) :1686-1696