References(117)
[1]
N Kamran, MS Alghamri, FJ Nunez, et al. Current state and future prospects of immunotherapy for glioma. Immunotherapy. 2018, 10(4): 317-339.
[2]
D Matias, J Balça-Silva, G Da Graça, et al. Microglia/astrocytes-glioblastoma crosstalk: Crucial molecular mechanisms and microenvironmental factors. Front Cell Neurosci. 2018, 12: 235.
[3]
T Miyazaki, E Ishikawa, M Matsuda, et al. Infiltration of CD163-positive macrophages in glioma tissues after treatment with anti-PD-L1 antibody and role of PI3Kγ inhibitor as a combination therapy with anti-PD-L1 antibody in in vivo model using temozolomide-resistant murine glioma-initiating cells. Brain Tumor Pathol. 2020, 37(2): 41-49.
[4]
HQ Wang, LY Zhang, IY Zhang, et al. S100B promotes glioma growth through chemoattraction of myeloid-derived macrophages. Clin Cancer Res. 2013, 19(14): 3764-3775.
[5]
T Muliaditan, J Caron, M Okesola, et al. Macrophages are exploited from an innate wound healing response to facilitate cancer metastasis. Nat Commun. 2018, 9(1): 2951.
[6]
A Mantovani, F Marchesi, A Malesci, et al. Tumour- associated macrophages as treatment targets in oncology. Nat Rev Clin Oncol. 2017, 14(7): 399-416.
[7]
H You, S Baluszek, B Kaminska. Supportive roles of brain macrophages in CNS metastases and assessment of new approaches targeting their functions. Theranostics. 2020, 10(7): 2949-2964.
[8]
AL Hudson, NR Parker, P Khong, et al. Glioblastoma recurrence correlates with increased APE1 and polarization toward an immuno-suppressive microenvironment. Front Oncol. 2018, 8: 314.
[9]
P Domingues, M González-Tablas, Á Otero, et al. Tumor infiltrating immune cells in gliomas and meningiomas. Brain Behav Immun. 2016, 53: 1-15.
[10]
LJM Perus, LA Walsh. Microenvironmental heterogeneity in brain malignancies. Front Immunol. 2019, 10: 2294.
[11]
JW Zhou, ZW Tang, SY Gao, et al. Tumor-associated macrophages: Recent insights and therapies. Front Oncol. 2020, 10: 188.
[12]
C Morrison. Immuno-oncologists eye up macrophage targets. Nat Rev Drug Discov. 2016, 15(6): 373-374.
[13]
PF Zhao, YH Wang, XJ Kang, et al. Dual-targeting biomimetic delivery for anti-glioma activity via remodeling the tumor microenvironment and directing macrophage-mediated immunotherapy. Chem Sci. 2018, 9(10): 2674-2689.
[14]
F Balkwill, A Mantovani. Inflammation and cancer: Back to Virchow? Lancet. 2001, 357(9255): 539-545.
[15]
D Hambardzumyan, DH Gutmann, H Kettenmann. The role of microglia and macrophages in glioma maintenance and progression. Nat Neurosci. 2016, 19(1): 20-27.
[16]
S Khan, S Mittal, K Mcgee, et al. Role of neutrophils and myeloid-derived suppressor cells in glioma progression and treatment resistance. Int J Mol Sci. 2020, 21(6): 1954.
[17]
E Gomez Perdiguero, K Klapproth, C Schulz, et al. Tissue-resident macrophages originate from yolk- sac-derived erythro-myeloid progenitors. Nature. 2015, 518(7540): 547-551.
[18]
F Alliot, I Godin, B Pessac. Microglia derive from progenitors, originating from the yolk sac, and which proliferate in the brain. Brain Res Dev Brain Res. 1999, 117(2): 145-152.
[19]
L Sevenich. Brain-resident microglia and blood-borne macrophages orchestrate central nervous system inflammation in neurodegenerative disorders and brain cancer. Front Immunol. 2018, 9: 697.
[20]
B Ajami, JL Bennett, C Krieger, et al. Infiltrating monocytes trigger EAE progression, but do not contribute to the resident microglia pool. Nat Neurosci. 2011, 14(9): 1142-1149.
[21]
PW Chen, P Bonaldo. Role of macrophage polarization in tumor angiogenesis and vessel normalization: implications for new anticancer therapies. Int Rev Cell Mol Biol. 2013, 301: 1-35.
[22]
SM Pyonteck, L Akkari, AJ Schuhmacher, et al. CSF-1R inhibition alters macrophage polarization and blocks glioma progression. Nat Med. 2013, 19(10): 1264-1272.
[23]
NN Dong, XY Shi, SH Wang, et al. M2 macrophages mediate sorafenib resistance by secreting HGF in a feed-forward manner in hepatocellular carcinoma. Br J Cancer. 2019, 121(1): 22-33.
[24]
NA Charles, EC Holland, R Gilbertson, et al. The brain tumor microenvironment. Glia. 2012, 60(3): 502-514.
[25]
Q Lahmar, J Keirsse, D Laoui, et al. Tissue-resident versus monocyte-derived macrophages in the tumor microenvironment. Biochim Biophys Acta. 2016, 1865(1): 23-34.
[26]
Y Shi, YF Ping, WC Zhou, et al. Tumour-associated macrophages secrete pleiotrophin to promote PTPRZ1 signalling in glioblastoma stem cells for tumour growth. Nat Commun. 2017, 8: 15080.
[27]
A Nishie, M Ono, T Shono, et al. Macrophage infiltration and heme oxygenase-1 expression correlate with angiogenesis in human gliomas. Clin Cancer Res. 1999, 5(5): 1107-1113.
[28]
RA Franklin, W Liao, A Sarkar, et al. The cellular and molecular origin of tumor-associated macrophages. Science. 2014, 344(6186): 921-925.
[29]
L Bingle, NJ Brown, CE Lewis. The role of tumour- associated macrophages in tumour progression: implications for new anticancer therapies. J Pathol. 2002, 196(3): 254-265.
[30]
FO Martinez, S Gordon. The M1 and M2 paradigm of macrophage activation: time for reassessment. F1000Prime Rep. 2014, 6: 13.
[31]
K Gabrusiewicz, A Ellert-Miklaszewska, M Lipko, et al. Characteristics of the alternative phenotype of microglia/macrophages and its modulation in experimental gliomas. PLoS One. 2011, 6(8): e23902.
[32]
T Kees, J Lohr, J Noack, et al. Microglia isolated from patients with glioma gain antitumor activities on poly (I:C) stimulation. Neuro Oncol. 2012, 14(1): 64-78.
[33]
A Mantovani, S Sozzani, M Locati, et al. Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes. Trends Immunol. 2002, 23(11): 549-555.
[34]
A Mantovani, A Sica, S Sozzani, et al. The chemokine system in diverse forms of macrophage activation and polarization. Trends Immunol. 2004, 25(12): 677-686.
[35]
S Müller, G Kohanbash, SJ Liu, et al. Single-cell profiling of human gliomas reveals macrophage ontogeny as a basis for regional differences in macrophage activation in the tumor microenvironment. Genome Biol. 2017, 18(1): 234.
[36]
Y Komohara, K Ohnishi, J Kuratsu, et al. Possible involvement of the M2 anti-inflammatory macrophage phenotype in growth of human gliomas. J Pathol. 2008, 216(1): 15-24.
[37]
OW Yeung, CM Lo, CC Ling, et al. Alternatively activated (M2) macrophages promote tumour growth and invasiveness in hepatocellular carcinoma. J Hepatol. 2015, 62(3): 607-616.
[38]
C Zhu, I Chrifi, D Mustafa, et al. CECR1-mediated cross talk between macrophages and vascular mural cells promotes neovascularization in malignant glioma. Oncogene. 2017, 36(38): 5356-5368.
[39]
L Pinton, S Magri, E Masetto, et al. Targeting of immunosuppressive myeloid cells from glioblastoma patients by modulation of size and surface charge of lipid nanocapsules. J Nanobiotechnol. 2020, 18: 31.
[40]
X Liu, F Chen, WB Li. Elevated expression of DOK3 indicates high suppressive immune cell infiltration and unfavorable prognosis of gliomas. Int Immunopharmacol. 2020, 83: 106400.
[41]
ZH Zhang, XM Huang, J Li, et al. Interleukin 10 promotes growth and invasion of glioma cells by up-regulating KPNA 2 in vitro. J Cancer Res Ther. 2019, 15(4): 927-932.
[42]
RV Lukas, C Juhász, DA Wainwright, et al. Imaging tryptophan uptake with positron emission tomography in glioblastoma patients treated with indoximod. J Neurooncol. 2019, 141(1): 111-120.
[43]
NF Brown, TJ Carter, D Ottaviani, et al. Harnessing the immune system in glioblastoma. Br J Cancer. 2018, 119(10): 1171-1181.
[44]
T Sun, YY Li, W Yang, et al. Histone deacetylase inhibition up-regulates MHC class I to facilitate cytotoxic T lymphocyte-mediated tumor cell killing in glioma cells. J Cancer. 2019, 10(23): 5638-5645.
[45]
WL Fu, WJ Wang, H Li, et al. High dimensional mass cytometry analysis reveals characteristics of the immunosuppressive microenvironment in diffuse astrocytomas. Front Oncol. 2020, 10: 78.
[46]
J Miska, C Lee-Chang, A Rashidi, et al. HIF-1α is a metabolic switch between glycolytic-driven migration and oxidative phosphorylation-driven immunosuppression of tregs in glioblastoma. Cell Rep. 2019, 27(1): 226-237.
[47]
J Wang, DY Li, HX Cang, et al. Crosstalk between cancer and immune cells: Role of tumor-associated macrophages in the tumor microenvironment. Cancer Med. 2019, 8(10): 4709-4721.
[48]
C Guruvayoorappan. Tumor versus tumor-associated macrophages: how hot is the link? Integr Cancer Ther. 2008, 7(2): 90-95.
[49]
TE Peterson, ND Kirkpatrick, YH Huang, et al. Dual inhibition of Ang-2 and VEGF receptors normalizes tumor vasculature and prolongs survival in glioblastoma by altering macrophages. Proc Natl Acad Sci USA. 2016, 113(16): 4470-4475.
[50]
R Tamura, T Tanaka, Y Akasaki, et al. The role of vascular endothelial growth factor in the hypoxic and immunosuppressive tumor microenvironment: perspectives for therapeutic implications. Med Oncol. 2019, 37(1): 2.
[51]
CL Wang, Y Li, HL Chen, et al. Inhibition of CYP4A by a novel flavonoid FLA-16 prolongs survival and normalizes tumor vasculature in glioma. Cancer Lett. 2017, 402: 131-141.
[52]
L Zhang, YY Xu, JT Sun, et al. M2-like tumor- associated macrophages drive vasculogenic mimicry through amplification of IL-6 expression in glioma cells. Oncotarget. 2017, 8(1): 819-832.
[53]
T Hori, T Sasayama, K Tanaka, et al. Tumor- associated macrophage related interleukin-6 in cerebrospinal fluid as a prognostic marker for glioblastoma. J Clin Neurosci. 2019, 68: 281-289.
[54]
S Brandenburg, A Müller, K Turkowski, et al. Resident microglia rather than peripheral macrophages promote vascularization in brain tumors and are source of alternative pro-angiogenic factors. Acta Neuropathol. 2016, 131(3): 365-378.
[55]
C Deligne, J Hachani, S Duban-Deweer, et al. Development of a human in vitro blood-brain tumor barrier model of diffuse intrinsic pontine glioma to better understand the chemoresistance. Fluids Barriers CNS. 2020, 17(1): 37.
[56]
WZ Lin, SH Wu, XC Chen, et al. Characterization of hypoxia signature to evaluate the tumor immune microenvironment and predict prognosis in glioma groups. Front Oncol. 2020, 10: 796.
[57]
SL Shang, XR Ji, LL Zhang, et al. Macrophage ABHD5 suppresses NFκB-dependent matrix metalloproteinase expression and cancer metastasis. Cancer Res. 2019, 79(21): 5513-5526.
[58]
SL Li, J Ma, Y Si, et al. Differential expression and functions of Ehm2 transcript variants in lung adenocarcinoma. Int J Oncol. 2019, 54(5): 1747-1758.
[59]
W Zhou, XJ Yu, S Sun, et al. Increased expression of MMP-2 and MMP-9 indicates poor prognosis in glioma recurrence. Biomedecine Pharmacother. 2019, 118: 109369.
[60]
YY Liu, XY Li, YP Zhang, et al. An miR- 340-5p-macrophage feedback loop modulates the progression and tumor microenvironment of glioblastoma multiforme. Oncogene. 2019, 38(49): 7399-7415.
[61]
CV Locarno, M Simonelli, C Carenza, et al. Role of myeloid cells in the immunosuppressive microenvironment in gliomas. Immunobiology. 2020, 225(1): 151853.
[62]
S Lee, E Lee, E Ko, et al. Tumor-associated macrophages secrete CCL2 and induce the invasive phenotype of human breast epithelial cells through upregulation of ERO1-α and MMP-9. Cancer Lett. 2018, 437: 25-34.
[63]
WB Fang, M Yao, G Brummer, et al. Targeted gene silencing of CCL2 inhibits triple negative breast cancer progression by blocking cancer stem cell renewal and M2 macrophage recruitment. Oncotarget. 2016, 7(31): 49349-49367.
[64]
ZH Chen, D Hambardzumyan. Immune microenvironment in glioblastoma subtypes. Front Immunol. 2018, 9: 1004.
[65]
SW Wang, C Chen, JL Li, et al. The CXCL12/ CXCR4 Axis confers temozolomide resistance to human glioblastoma cells via up-regulation of FOXM1. J Neurol Sci. 2020, 414: 116837.
[66]
G Sokratous, S Polyzoidis, K Ashkan. Immune infiltration of tumor microenvironment following immunotherapy for glioblastoma multiforme. Hum Vaccin Immunother. 2017, 13(11): 2575-2582.
[67]
AM Stessin, MG Clausi, ZR Zhao, et al. Repolarized macrophages, induced by intermediate stereotactic dose radiotherapy and immune checkpoint blockade, contribute to long-term survival in glioma-bearing mice. J Neurooncol. 2020, 147(3): 547-555.
[68]
J Ye, YF Yang, WJ Dong, et al. Drug-free mannosylated liposomes inhibit tumor growth by promoting the polarization of tumor-associated macrophages. Int J Nanomedicine. 2019, 14: 3203-3220.
[69]
CI Chang, JC Liao, L Kuo. Macrophage arginase promotes tumor cell growth and suppresses nitric oxide-mediated tumor cytotoxicity. Cancer Res. 2001, 61(3): 1100-1106.
[70]
A Ellert-Miklaszewska, P Wisniewski, M Kijewska, et al. Tumour-processed osteopontin and lactadherin drive the protumorigenic reprogramming of microglia and glioma progression. Oncogene. 2016, 35(50): 6366-6377.
[71]
SL Shiao, AP Ganesan, HS Rugo, et al. Immune microenvironments in solid tumors: new targets for therapy. Genes Dev. 2011, 25(24): 2559-2572.
[72]
SK Biswas, A Mantovani. Macrophage plasticity and interaction with lymphocyte subsets: cancer as a paradigm. Nat Immunol. 2010, 11(10): 889-896.
[73]
M Zhang, G Hutter, SA Kahn, et al. Anti-CD47 treatment stimulates phagocytosis of glioblastoma by M1 and M2 polarized macrophages and promotes M1 polarized macrophages in vivo. PLoS One. 2016, 11(4): e0153550.
[74]
XP Mo, ZN Zheng, Y He, et al. Antiglioma via regulating oxidative stress and remodeling tumor- associated macrophage using lactoferrin-mediated biomimetic codelivery of simvastatin/fenretinide. J Control Release. 2018, 287: 12-23.
[75]
MH Park, SY Kwon, JE Choi, et al. Intratumoral CD103-positive tumor-infiltrating lymphocytes are associated with favorable prognosis in patients with triple-negative breast cancer. Histopathology. 2020, in press, .
[76]
N Wang, HW Liang, K Zen. Molecular mechanisms that influence the macrophage m1-m2 polarization balance. Front Immunol. 2014, 5: 614.
[77]
G Natoli, S Monticelli. Macrophage activation: glancing into diversity. Immunity. 2014, 40(2): 175-177.
[78]
A Sica, A Mantovani. Macrophage plasticity and polarization: in vivo veritas. J Clin Invest. 2012, 122(3): 787-795.
[79]
Y Degboé, B Rauwel, M Baron, et al. Polarization of rheumatoid macrophages by TNF targeting through an IL-10/STAT3 mechanism. Front Immunol. 2019, 10: 3.
[80]
L Zhang, TE Peterson, VM Lu, et al. Antitumor activity of novel pyrazole-based small molecular inhibitors of the STAT3 pathway in patient derived high grade glioma cells. PLoS One. 2019, 14(7): e0220569.
[81]
A Mantovani, G Germano, F Marchesi, et al. Cancer-promoting tumor-associated macrophages: new vistas and open questions. Eur J Immunol. 2011, 41(9): 2522-2525.
[82]
N Tajik, M Tajik, I Mack, et al. The potential effects of chlorogenic acid, the main phenolic components in coffee, on health: a comprehensive review of the literature. Eur J Nutr. 2017, 56(7): 2215-2244.
[83]
NN Xue, Q Zhou, M Ji, et al. Chlorogenic acid inhibits glioblastoma growth through repolarizating macrophage from M2 to M1 phenotype. Sci Rep. 2017, 7: 39011.
[84]
N Daftarian, S Zandi, G Piryaie, et al. Peripheral blood CD163(+) monocytes and soluble CD163 in dry and neovascular age-related macular degeneration. FASEB J. 2020, 34(6): 8001-8011.
[85]
JJ Park, SJ Hwang, JH Park, et al. Chlorogenic acid inhibits hypoxia-induced angiogenesis via down- regulation of the HIF-1α/AKT pathway. Cell Oncol. 2015, 38(2): 111-118.
[86]
G Hutter, J Theruvath, CM Graef, et al. Microglia are effector cells of CD47-SIRPα antiphagocytic axis disruption against glioblastoma. Proc Natl Acad Sci USA. 2019, 116(3): 997-1006.
[87]
F Li, B Lv, Y Liu, et al. Blocking the CD47-SIRPα axis by delivery of anti-CD47 antibody induces antitumor effects in glioma and glioma stem cells. Oncoimmunology. 2018, 7(2): e1391973.
[88]
LB Sun, HX Liang, WD Yu, et al. Increased invasive phenotype of CSF-1R expression in glioma cells via the ERK1/2 signaling pathway. Cancer Gene Ther. 2019, 26(5/6): 136-144.
[89]
KR Wiehagen, NM Girgis, DH Yamada, et al. Combination of CD40 agonism and CSF-1R blockade reconditions tumor-associated macrophages and drives potent antitumor immunity. Cancer Immunol Res. 2017, 5(12): 1109-1121.
[90]
T Hagemann, T Lawrence, I McNeish, et al. “Re-educating” tumor-associated macrophages by targeting NF-κB. J Exp Med. 2008, 205(6): 1261-1268.
[91]
KP Zeligs, MK Neuman, CM Annunziata. Molecular pathways: the balance between cancer and the immune system challenges the therapeutic specificity of targeting nuclear factor-κB signaling for cancer treatment. Clin Cancer Res. 2016, 22(17): 4302-4308.
[92]
T Barberi, A Martin, R Suresh, et al. Absence of host NF-κB p50 induces murine glioblastoma tumor regression, increases survival, and decreases T-cell induction of tumor-associated macrophage M2 polarization. Cancer Immunol Immunother. 2018, 67(10): 1491-1503.
[93]
X Cui, RT Morales, WY Qian, et al. Hacking macrophage-associated immunosuppression for regulating glioblastoma angiogenesis. Biomaterials. 2018, 161: 164-178.
[94]
WC Zhou, SQ Ke, Z Huang, et al. Periostin secreted by glioblastoma stem cells recruits M2 tumour- associated macrophages and promotes malignant growth. Nat Cell Biol. 2015, 17(2): 170-182.
[95]
G Acker, J Zollfrank, C Jelgersma, et al. The CXCR2/CXCL2 signalling pathway - An alternative therapeutic approach in high-grade glioma. Eur J Cancer. 2020, 126: 106-115.
[96]
A Tivnan, T Heilinger, EC Lavelle, et al. Advances in immunotherapy for the treatment of glioblastoma. J Neurooncol. 2017, 131(1): 1-9.
[97]
W Hugo, JM Zaretsky, L Sun, et al. Genomic and transcriptomic features of response to anti-PD-1 therapy in metastatic melanoma. Cell. 2017, 168(3): 542.
[98]
S Yao, YW Zhu, GF Zhu, et al. B7-h2 is a costimulatory ligand for CD28 in human. Immunity. 2011, 34(5): 729-740.
[99]
S Chikuma. Basics of PD-1 in self-tolerance, infection, and cancer immunity. Int J Clin Oncol. 2016, 21(3): 448-455.
[100]
ME Keir, MJ Butte, GJ Freeman, et al. PD-1 and its ligands in tolerance and immunity. Annu Rev Immunol. 2008, 26: 677-704.
[101]
FL Ricklefs, Q Alayo, H Krenzlin, et al. Immune evasion mediated by PD-L1 on glioblastoma-derived extracellular vesicles. Sci Adv. 2018, 4(3): eaar2766.
[102]
MC Speranza, C Passaro, F Ricklefs, et al. Preclinical investigation of combined gene-mediated cytotoxic immunotherapy and immune checkpoint blockade in glioblastoma. Neuro-oncology. 2018, 20(2): 225-235.
[103]
BL Dai, N Qi, JC Li, et al. Temozolomide combined with PD-1 Antibody therapy for mouse orthotopic glioma model. Biochem Biophys Res Commun. 2018, 501(4): 871-876.
[104]
B Lu, Y Zhou, ZZ Su, et al. Effect of CCL2 siRNA on proliferation and apoptosis in the U251 human glioma cell line. Mol Med Rep. 2017, 16(3): 3387-3394.
[105]
A Vakilian, H Khorramdelazad, P Heidari, et al. CCL2/CCR2 signaling pathway in glioblastoma multiforme. Neurochem Int. 2017, 103: 1-7.
[106]
JA Flores-Toro, DF Luo, A Gopinath, et al. CCR2 inhibition reduces tumor myeloid cells and unmasks a checkpoint inhibitor effect to slow progression of resistant murine gliomas. Proc Natl Acad Sci USA. 2020, 117(2): 1129-1138.
[107]
C Hanna, TA Lawrie, E Rogozińska, et al. Treatment of newly diagnosed glioblastoma in the elderly: a network meta-analysis. Cochrane Database Syst Rev. 2020, 3: CD013261.
[108]
X Feng, S Liu, D Chen, et al. Rescue of cognitive function following fractionated brain irradiation in a novel preclinical glioma model. Elife. 2018, 7: e38865.
[109]
D Yan, J Kowal, L Akkari, et al. Inhibition of colony stimulating factor-1 receptor abrogates microenvironment-mediated therapeutic resistance in gliomas. Oncogene. 2017, 36(43): 6049-6058.
[110]
J Yin, KL Valin, ML Dixon, et al. The role of microglia and macrophages in CNS homeostasis, autoimmunity, and cancer. J Immunol Res. 2017, 2017: 5150678.
[111]
A Lopez, ML Cruz, G Chompre, et al. Influence of stress on the vitamin D-vitamin D receptor system, macrophages, and the local inflammatory milieu in endometriosis. Reprod Sci. 2020, in press, .
[112]
K Baidžajevas, É Hadadi, B Lee, et al. Macrophage polarisation associated with atherosclerosis differentially affects their capacity to handle lipids. Atherosclerosis. 2020, 305: 10-18.
[113]
M Maraux, A Gaillardet, A Gally, et al. Human primary neutrophil mRNA does not contaminate human resolving macrophage mRNA after efferocytosis. J Immunol Methods. 2020, 483: 112810.
[114]
KL Trout, A Holian. Multinucleated giant cell phenotype in response to stimulation. Immunobiology. 2020, 225(3): 151952.
[115]
D Gomez-Zepeda, M Taghi, JM Scherrmann, et al. ABC transporters at the blood-brain interfaces, their study models, and drug delivery implications in gliomas. Pharmaceutics. 2019, 12(1): E20.
[116]
SY Fu, M Liang, YL Wang, et al. Dual-modified novel biomimetic nanocarriers improve targeting and therapeutic efficacy in glioma. ACS Appl Mater Interfaces. 2019, 11(2): 1841-1854.
[117]
L Cui, YL Wang, M Liang, et al. Dual-modified natural high density lipoprotein particles for systemic glioma-targeting drug delivery. Drug Deliv. 2018, 25(1): 1865-1876.