Therapeutic Targeting of Glioblastoma and the Interactions with Its Microenvironment

被引:4
作者
Genoud, Vassilis [1 ,2 ,3 ,4 ]
Kinnersley, Ben [1 ,2 ]
Brown, Nicholas F. [1 ,5 ]
Ottaviani, Diego [1 ,2 ]
Mulholland, Paul [1 ,2 ]
机构
[1] UCL, Glioblastoma Res Grp, London WC1E 6DD, England
[2] Univ Coll London Hosp, Dept Oncol, London NW1 2PB, England
[3] Univ Hosp Geneva, Dept Oncol, CH-1205 Geneva, Switzerland
[4] Univ Geneva, Ctr Translat Res Onco Haematol, CH-1205 Geneva, Switzerland
[5] Guys & St Thomas NHS Fdn Trust, Guys Canc, London SE1 3SS, England
基金
瑞士国家科学基金会;
关键词
glioblastoma (GBM); heterogeneity; tumour microenvironment (TME); myeloid cells; microglia; tumour associated macrophages (TAMs); therapeutic targeting; TUMOR-INFILTRATING LYMPHOCYTES; BLOOD-BRAIN-BARRIER; CANCER STEM-CELLS; REGULATORY T-CELLS; HUMAN GLIOMA; CHEMOTHERAPY RESISTANCE; RECURRENT GLIOBLASTOMA; ANTITUMOR IMMUNITY; SUPPRESSOR-CELLS; GENOMIC ANALYSIS;
D O I
10.3390/cancers15245790
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Glioblastoma (GBM) is the most aggressive brain tumour. Patients with GBM have a dismal survival and there is a distinct lack of curative treatments. We are increasingly understanding that the GBM tumour is composed not only of tumour cells but a complex tumour microenvironment (TME) of neuronal, glial and immune cells. Research into this area is important because the diversity of tumour cells and interactions with the TME contribute to the aggressiveness and treatment resistance of GBM. In this work, we review the multiple types of cells forming GBM and their interactions and provide examples of how our improved understanding can suggest potential new treatment strategies for this devastating disease.Abstract Glioblastoma (GBM) is the most common primary malignant brain tumour, and it confers a dismal prognosis despite intensive multimodal treatments. Whilst historically, research has focussed on the evolution of GBM tumour cells themselves, there is growing recognition of the importance of studying the tumour microenvironment (TME). Improved characterisation of the interaction between GBM cells and the TME has led to a better understanding of therapeutic resistance and the identification of potential targets to block these escape mechanisms. This review describes the network of cells within the TME and proposes treatment strategies for simultaneously targeting GBM cells, the surrounding immune cells, and the crosstalk between them.
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页数:18
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共 166 条
[1]   Single-cell analysis of human glioma and immune cells identifies S100A4 as an immunotherapy target [J].
Abdelfattah, Nourhan ;
Kumar, Parveen ;
Wang, Caiyi ;
Leu, Jia-Shiun ;
Flynn, William F. ;
Gao, Ruli ;
Baskin, David S. ;
Pichumani, Kumar ;
Ijare, Omkar B. ;
Wood, Stephanie L. ;
Powell, Suzanne Z. ;
Haviland, David L. ;
Kerrigan, Brittany C. Parker ;
Lang, Frederick F. ;
Prabhu, Sujit S. ;
Huntoon, Kristin M. ;
Jiang, Wen ;
Kim, Betty Y. S. ;
George, Joshy ;
Yun, Kyuson .
NATURE COMMUNICATIONS, 2022, 13 (01)
[2]   A HIF-independent, CD133-mediated mechanism of cisplatin resistance in glioblastoma cells [J].
Ahmed, Eroje M. ;
Bandopadhyay, Gagori ;
Coyle, Beth ;
Grabowska, Anna .
CELLULAR ONCOLOGY, 2018, 41 (03) :319-328
[3]   HER2-Specific Chimeric Antigen Receptor-Modified Virus-Specific T Cells for Progressive Glioblastoma A Phase 1 Dose-Escalation Trial [J].
Ahmed, Nabil ;
Brawley, Vita ;
Hegde, Meenakshi ;
Bielamowicz, Kevin ;
Kalra, Mamta ;
Landi, Daniel ;
Robertson, Catherine ;
Gray, Tara L. ;
Diouf, Oumar ;
Wakefield, Amanda ;
Ghazi, Alexia ;
Gerken, Claudia ;
Yi, Zhongzhen ;
Ashoori, Aidin ;
Wu, Meng-Fen ;
Liu, Hao ;
Rooney, Cliona ;
Dotti, Gianpietro ;
Gee, Adrian ;
Su, Jack ;
Kew, Yvonne ;
Baskin, David ;
Zhang, Yi Jonathan ;
New, Pamela ;
Grilley, Bambi ;
Stojakovic, Milica ;
Hicks, John ;
Powell, Suzanne Z. ;
Brenner, Malcolm K. ;
Heslop, Helen E. ;
Grossman, Robert ;
Wels, Winfried S. ;
Gottschalk, Stephen .
JAMA ONCOLOGY, 2017, 3 (08) :1094-1101
[4]   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)
[5]   Global immune fingerprinting in glioblastoma patient peripheral blood reveals immune-suppression signatures associated with prognosis [J].
Alban, Tyler J. ;
Alvarado, Alvaro G. ;
Sorensen, Mia D. ;
Bayik, Defne ;
Volovetz, Josephine ;
Serbinowski, Emily ;
Mulkearns-Hubert, Erin E. ;
Sinyuk, Maksim ;
Hale, James S. ;
Onzi, Giovana R. ;
McGraw, Mary ;
Huang, Pengjing ;
Grabowski, Matthew M. ;
Wathen, Connor A. ;
Ahluwalia, Manmeet S. ;
Radivoyevitch, Tomas ;
Kornblum, Harley, I ;
Kristensen, Bjarne W. ;
Vogelbaum, Michael A. ;
Lathia, Justin D. .
JCI INSIGHT, 2018, 3 (21)
[6]   Single-cell profiling of myeloid cells in glioblastoma across species and disease stage reveals macrophage competition and specialization [J].
Antunes, Ana Rita Pombo ;
Scheyltjens, Isabelle ;
Lodi, Francesca ;
Messiaen, Julie ;
Antoranz, Asier ;
Duerinck, Johnny ;
Kancheva, Daliya ;
Martens, Liesbet ;
De Vlaminck, Karen ;
Van Hove, Hannah ;
Hansen, Signe Schmidt Kjolner ;
Bosisio, Francesca Maria ;
Van der Borght, Koen ;
De Vleeschouwer, Steven ;
Sciot, Raf ;
Bouwens, Luc ;
Verfaillie, Michiel ;
Vandamme, Niels ;
Vandenbroucke, Roosmarijn E. ;
De Wever, Olivier ;
Saeys, Yvan ;
Guilliams, Martin ;
Gysemans, Conny ;
Neyns, Bart ;
De Smet, Frederik ;
Lambrechts, Diether ;
Van Ginderachter, Jo A. ;
Movahedi, Kiavash .
NATURE NEUROSCIENCE, 2021, 24 (04) :595-610
[7]   The role of glioma stem cells in chemotherapy resistance and glioblastoma multiforme recurrence [J].
Auffinger, Brenda ;
Spencer, Drew ;
Pytel, Peter ;
Ahmed, Atique U. ;
Lesniak, Maciej S. .
EXPERT REVIEW OF NEUROTHERAPEUTICS, 2015, 15 (07) :741-752
[8]   Temozolomide preferentially depletes cancer stem cells in glioblastoma [J].
Beier, Dagmar ;
Roehrl, Stefanie ;
Pillai, Deepu R. ;
Schwarz, Stefanie ;
Kunz-Schughart, Leoni A. ;
Leukel, Petra ;
Proescholdt, Martin ;
Brawanski, Alexander ;
Bogdahn, Ulrich ;
Trampe-Kieslich, Ariane ;
Giebel, Bernd ;
Wischhusen, Joerg ;
Reifenberger, Guido ;
Hau, Peter ;
Beier, Christoph P. .
CANCER RESEARCH, 2008, 68 (14) :5706-5715
[9]   Programmed death ligand 1 expression and tumor-infiltrating lymphocytes in glioblastoma [J].
Berghoff, Anna Sophie ;
Kiesel, Barbara ;
Widhalm, Georg ;
Rajky, Orsolya ;
Ricken, Gerda ;
Woehrer, Adelheid ;
Dieckmann, Karin ;
Filipits, Martin ;
Brandstetter, Anita ;
Weller, Michael ;
Kurscheid, Sebastian ;
Hegi, Monika E. ;
Zielinski, Christoph C. ;
Marosi, Christine ;
Hainfellner, Johannes A. ;
Preusser, Matthias ;
Wick, Wolfgang .
NEURO-ONCOLOGY, 2015, 17 (08) :1064-1075
[10]   Trivalent CAR T cells overcome interpatient antigenic variability in glioblastoma [J].
Bielamowicz, Kevin ;
Fousek, Kristen ;
Byrd, Tiara T. ;
Samaha, Hebatalla ;
Mukherjee, Malini ;
Aware, Nikita ;
Wu, Meng-Fen ;
Orange, Jordan S. ;
Sumazin, Pavel ;
Man, Tsz-Kwong ;
Joseph, Sujith K. ;
Hegde, Meenakshi ;
Ahmed, Nabil .
NEURO-ONCOLOGY, 2018, 20 (04) :506-518