Toll-Like Receptors as Therapeutic Targets in Central Nervous System Tumors

被引:18
作者
Abarca-Merlin, D. M. [1 ,2 ,3 ]
Maldonado-Bernal, C. [3 ]
Alvarez-Arellano, L. [4 ]
机构
[1] Hosp Infantil Mexico Dr Federico Gomez, Lab Neurociencias, Mexico City, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Fac Quim, Mexico City, DF, Mexico
[3] Hosp Infantil Mexico Dr Federico Gomez, Lab Invest Inmunol & Prote, Mexico City, DF, Mexico
[4] CONACYT Hosp Infantil Mexico Federico Gomez, Mexico City, DF, Mexico
关键词
CANCER; CELLS;
D O I
10.1155/2019/5286358
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
In recent years, progress has been made in understanding the pathological, genetic, and molecular heterogeneity of central nervous system (CNS) tumors. However, improvements in risk classification, prognosis, and treatment have not been sufficient. Currently, great importance has been placed to the tumor microenvironment and the immune system, which are very important components that influence the establishment and development of tumors. Toll-like receptors (TLRs) are innate immunite system sensors of a wide variety of molecules, such as those associated with microorganisms and danger signals. TLRs are expressed on many cells, including immune cells and nonimmune cells such as neurons and cancer cells. In the tumor microenvironment, activation of TLRs plays dual antitumoral (dendritic cells, cytotoxic T cells, and natural killer cells activation) and protumoral effects (tumor cell proliferation, survival, and resistance to chemotherapy) and constitutes an area of opportunities and challenges in the development of new therapeutic strategies. Several clinical trials have been carried out, and others are currently in process; however, the results obtained to date have been contradictory and have not led to a definitive position about the use of TLR agonists in adjuvant therapy during the treatment of central nervous system (CNS) tumors. In this review, we focus on recent advances in TLR agonists as immunotherapies for treatment of CNS tumors.
引用
收藏
页数:9
相关论文
共 82 条
[1]
Glioblastoma Cancer Stem Cells Evade Innate Immune Suppression of Self-Renewal through Reduced TLR4 Expression [J].
Alvarado, Alvaro G. ;
Thiagarajan, Praveena S. ;
Mulkearns-Hubert, Erin E. ;
Silver, Daniel J. ;
Hale, James S. ;
Alban, Tyler J. ;
Turaga, Soumya M. ;
Jarrar, Awad ;
Reizes, Ofer ;
Longworth, Michelle S. ;
Vogelbaum, Michael A. ;
Lathia, Justin D. .
CELL STEM CELL, 2017, 20 (04) :450-+
[2]
Pivotal role of high-mobility group box 1 (HMGB1) signaling pathways in glioma development and progression [J].
Angelopoulou, Efthalia ;
Piperi, Christina ;
Adamopoulos, Christos ;
Papavassiliou, Athanasios G. .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2016, 94 (08) :867-874
[3]
Cultured astrocytes express toll-like receptors for bacterial products [J].
Bowman, CC ;
Rasley, A ;
Tranguch, SL ;
Marriott, I .
GLIA, 2003, 43 (03) :281-291
[4]
Broad expression of Toll-like receptors in the human central nervous system [J].
Bsibsi, M ;
Ravid, R ;
Gveric, D ;
van Noort, JM .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2002, 61 (11) :1013-1021
[5]
c-Jun N-terminal kinases differentially regulate TNF- and TLRs-mediated necroptosis through their kinase-dependent and -independent activities [J].
Cao, Mengtao ;
Chen, Fei ;
Xie, Ni ;
Cao, Meng-Yao ;
Chen, Pengfei ;
Lou, Qi ;
Zhao, Yanli ;
He, Chen ;
Zhang, Shuyuan ;
Song, Xinyang ;
Sun, Yu ;
Zhu, Weimin ;
Mou, Lisha ;
Luan, Shaodong ;
Gao, Hanchao .
CELL DEATH & DISEASE, 2018, 9
[6]
Phase 1 trial of a CpG oligodeoxynucleotide for patients with recurrent glioblastoma [J].
Carpentier, A ;
Laigle-Donadey, F ;
Zohar, S ;
Capelle, L ;
Behin, A ;
Tibi, A ;
Martin-Duverneuil, N ;
Sanson, M ;
Lacomblez, L ;
Taillibert, S ;
Puybasset, L ;
Van Effenterre, R ;
Delattre, JY ;
Carpentier, AF .
NEURO-ONCOLOGY, 2006, 8 (01) :60-66
[7]
Carpentier AF, 2000, CLIN CANCER RES, V6, P2469
[8]
Intracerebral administration of CpG oligonucleotide for patients with recurrent glioblastoma: a phase II study [J].
Carpentier, Alexandre ;
Metellus, Philippe ;
Ursu, Renata ;
Zohar, Sarah ;
Lafitte, Francois ;
Barrie, Maryline ;
Meng, Yuxia ;
Richard, Margaretha ;
Parizot, Christophe ;
Laigle-Donadey, Florence ;
Gorochov, Guy ;
Psimaras, Dimitri ;
Sanson, Marc ;
Tibi, Annick ;
Chinot, Olivier ;
Carpentier, Antoine F. .
NEURO-ONCOLOGY, 2010, 12 (04) :401-408
[9]
Differential activation of astrocytes by innate and adaptive immune stimuli [J].
Carpentier, PA ;
Begolka, WS ;
Olson, JK ;
Elhofy, A ;
Karpus, WJ ;
Miller, SD .
GLIA, 2005, 49 (03) :360-374
[10]
Casili Giovanna, 2018, Oncotarget, V9, P37564, DOI 10.18632/oncotarget.26500