Targeting Tumor Associated Macrophages to Overcome Conventional Treatment Resistance in Glioblastoma

被引:57
作者
Gregoire, Helene [1 ]
Roncali, Loris [1 ]
Rousseau, Audrey [1 ,2 ]
Cherel, Michel [3 ]
Delneste, Yves [1 ,4 ]
Jeannin, Pascale [1 ,4 ]
Hindre, Francois [1 ,5 ]
Garcion, Emmanuel [1 ,6 ]
机构
[1] Univ Angers, Univ Nantes, INSERM, CRCINA, Angers, France
[2] CHU Angers, Dept Pathol Cellulaire & Tissulaire, Angers, France
[3] Univ Nantes, Univ Angers, INSERM, CRCINA, Nantes, France
[4] CHU Angers, Lab Immunol & Allergol, Angers, France
[5] Univ Angers, SFR ICAT, Plateforme Radiobiol & Imagerie Expt, PRIMEX, Angers, France
[6] Univ Angers, SFR ICAT, Plateforme Anal Cellulaires & Mol, PACeM, Angers, France
关键词
glioblastoma; macrophages; microglia; resistance; radiation; crosstalks; tumor-associated macrophage; GLIOMA-INFILTRATING MICROGLIA/MACROPHAGES; HIGH-GRADE GLIOMAS; CHEMOKINE LIGAND 2; MONOCLONAL-ANTIBODY; BREAST-CANCER; OPEN-LABEL; ADJUVANT TEMOZOLOMIDE; RESIDENT MICROGLIA; SUPPRESSOR-CELLS; MYELOID CELLS;
D O I
10.3389/fphar.2020.00368
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Glioblastoma (GB) is the most common and devastating form of brain cancer. Despite conventional treatments, progression or recurrences are systematic. In recent years, immunotherapies have emerged as an effective treatment in a number of cancers, leaving the question of their usefulness also faced with the particular case of brain tumors. The challenge here is major not only because the brain is the seat of our consciousness but also because of its isolation by the blood-brain barrier and the presence of a unique microenvironment that constitutes the central nervous system (CNS) with very specific constituent or patrolling cells. Much of the microenvironment is made up of immune cells or inflammation. Among these, tumor-associated macrophages (TAMs) are of significant interest as they are often involved in facilitating tumor progression as well as the development of resistance to standard therapies. In this review, the ubiquity of TAMs in GB will be discussed while the specific case of microglia resident in the brain will be also emphasized. In addition, the roles of TAMs as accomplices in the progression of GB and resistance to treatment will be presented. Finally, clinical trials targeting TAMs as a means of treating cancer will be discussed.
引用
收藏
页数:17
相关论文
共 151 条
  • [1] Canonical NFκB signaling in myeloid cells is required for the glioblastoma growth
    Achyut, B. R.
    Angara, Kartik
    Jain, Meenu
    Borin, Thaiz F.
    Rashid, Mohammad H.
    Iskander, A. S. M.
    Ara, Roxan
    Kolhe, Ravindra
    Howard, Shelby
    Venugopal, Natasha
    Rodriguez, Paulo C.
    Bradford, Jennifer W.
    Arbab, Ali S.
    [J]. SCIENTIFIC REPORTS, 2017, 7
  • [2] Topical TLR7 Agonist Imiquimod Can Induce Immune-Mediated Rejection of Skin Metastases in Patients with Breast Cancer
    Adams, Sylvia
    Kozhaya, Lina
    Martiniuk, Frank
    Meng, Tze-Chiang
    Chiriboga, Luis
    Liebes, Leonard
    Hochman, Tsivia
    Shuman, Nicholas
    Axelrod, Deborah
    Speyer, James
    Novik, Yelena
    Tiersten, Amy
    Goldberg, Judith D.
    Formenti, Silvia C.
    Bhardwaj, Nina
    Unutmaz, Derya
    Demaria, Sandra
    [J]. CLINICAL CANCER RESEARCH, 2012, 18 (24) : 6748 - 6757
  • [3] [Anonymous], STEM CELLS
  • [4] The p53 Isoform Δ133p53β Promotes Cancer Stem Cell Potential
    Arsic, Nikola
    Gadea, Gilles
    Lagerqvist, E. Louise
    Busson, Muriel
    Cahuzac, Nathalie
    Brock, Carsten
    Hollande, Frederic
    Gire, Veronique
    Pannequin, Julie
    Roux, Pierre
    [J]. STEM CELL REPORTS, 2015, 4 (04): : 531 - 540
  • [5] Role of Human Macrophage Polarization in Inflammation during Infectious Diseases
    Atri, Chiraz
    Guerfali, Fatma Z.
    Laouini, Dhafer
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2018, 19 (06):
  • [6] Interferon-γ induces apoptosis and augments the expression of Fas and Fas ligand by microglia in vitro
    Badie, B
    Schartner, J
    Vorpahl, J
    Preston, K
    [J]. EXPERIMENTAL NEUROLOGY, 2000, 162 (02) : 290 - 296
  • [7] A Breakdown in Metabolic Reprogramming Causes Microglia Dysfunction in Alzheimer's Disease
    Baik, Sung Hoon
    Kang, Seokjo
    Lee, Woochan
    Choi, Hayoung
    Chung, Sunwoo
    Kim, Jong-Il
    Mook-Jung, Inhee
    [J]. CELL METABOLISM, 2019, 30 (03) : 493 - +
  • [8] Absence of host NF-κB p50 induces murine glioblastoma tumor regression, increases survival, and decreases T-cell induction of tumor-associated macrophage M2 polarization
    Barberi, Theresa
    Martin, Allison
    Suresh, Rahul
    Barakat, David J.
    Harris-Bookman, Sarah
    Drake, Charles G.
    Lim, Michael
    Friedman, Alan D.
    [J]. CANCER IMMUNOLOGY IMMUNOTHERAPY, 2018, 67 (10) : 1491 - 1503
  • [9] Mesenchymal Differentiation Mediated by NF-κB Promotes Radiation Resistance in Glioblastoma
    Bhat, Krishna P. L.
    Balasubramaniyan, Veerakumar
    Vaillant, Brian
    Ezhilarasan, Ravesanker
    Hummelink, Karlijn
    Hollingsworth, Faith
    Wani, Khalida
    Heathcock, Lindsey
    James, Johanna D.
    Goodman, Lindsey D.
    Conroy, Siobhan
    Long, Lihong
    Lelic, Nina
    Wang, Suzhen
    Gumin, Joy
    Raj, Divya
    Kodama, Yoshinori
    Raghunathan, Aditya
    Olar, Adriana
    Joshi, Kaushal
    Pelloski, Christopher E.
    Heimberger, Amy
    Kim, Se Hoon
    Cahill, Daniel P.
    Rao, Ganesh
    Den Dunnen, Wilfred F. A.
    Boddeke, Hendrikus W. G. M.
    Phillips, Heidi S.
    Nakano, Ichiro
    Lang, Frederick F.
    Colman, Howard
    Sulman, Erik P.
    Aldape, Kenneth
    [J]. CANCER CELL, 2013, 24 (03) : 331 - 346
  • [10] Macrophage plasticity and interaction with lymphocyte subsets: cancer as a paradigm
    Biswas, Subhra K.
    Mantovani, Alberto
    [J]. NATURE IMMUNOLOGY, 2010, 11 (10) : 889 - 896