Literature DB >> 35411434

Cellular Conversations in Glioblastoma Progression, Diagnosis and Treatment.

Ali Karimi Sisakht1,2, Mohammad Malekan1,3,4, Farbod Ghobadinezhad1,5,6, Seyedeh Negar Mousavi Firouzabadi1,7, Ameneh Jafari8,9, Seyed Mohammad Ali Mirazimi10,11, Banafshe Abadi1,12, Rana Shafabakhsh13, Hamed Mirzaei14.   

Abstract

Glioblastoma (GBM) is the most frequent malignancy among primary brain tumors in adults and one of the worst 5-year survival rates (< 7%) among all human cancers. Till now, treatments that target particular cell or intracellular metabolism have not improved patients' survival. GBM recruits healthy brain cells and subverts their processes to create a microenvironment that contributes to supporting tumor progression. This microenvironment encompasses a complex network in which malignant cells interact with each other and with normal and immune cells to promote tumor proliferation, angiogenesis, metastasis, immune suppression, and treatment resistance. Communication can be direct via cell-to-cell contact, mainly through adhesion molecules, tunneling nanotubes, gap junctions, or indirect by conventional paracrine signaling by cytokine, neurotransmitter, and extracellular vesicles. Understanding these communication routes could open up new avenues for the treatment of this lethal tumor. Hence, therapeutic approaches based on glioma cells` communication have recently drawn attention. This review summarizes recent findings on the crosstalk between glioblastoma cells and their tumor microenvironment, and the impact of this conversation on glioblastoma progression. We also discuss the mechanism of communication of glioma cells and their importance as therapeutic targets and diagnostic and prognostic biomarkers. Overall, understanding the biological mechanism of specific interactions in the tumor microenvironment may help in predicting patient prognosis and developing novel therapeutic strategies to target GBM.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Cellular mechanism; Glioblastoma; Therapy

Year:  2022        PMID: 35411434     DOI: 10.1007/s10571-022-01212-9

Source DB:  PubMed          Journal:  Cell Mol Neurobiol        ISSN: 0272-4340            Impact factor:   5.046


  156 in total

1.  Glioma stem cells promote radioresistance by preferential activation of the DNA damage response.

Authors:  Shideng Bao; Qiulian Wu; Roger E McLendon; Yueling Hao; Qing Shi; Anita B Hjelmeland; Mark W Dewhirst; Darell D Bigner; Jeremy N Rich
Journal:  Nature       Date:  2006-10-18       Impact factor: 49.962

2.  Resident microglia rather than peripheral macrophages promote vascularization in brain tumors and are source of alternative pro-angiogenic factors.

Authors:  Susan Brandenburg; Annett Müller; Kati Turkowski; Yordan T Radev; Sergej Rot; Christin Schmidt; Alexander D Bungert; Güliz Acker; Anne Schorr; Andreas Hippe; Kelly Miller; Frank L Heppner; Bernhard Homey; Peter Vajkoczy
Journal:  Acta Neuropathol       Date:  2015-12-30       Impact factor: 17.088

Review 3.  Multidimensional communication in the microenvirons of glioblastoma.

Authors:  Marike L Broekman; Sybren L N Maas; Erik R Abels; Thorsten R Mempel; Anna M Krichevsky; Xandra O Breakefield
Journal:  Nat Rev Neurol       Date:  2018-08       Impact factor: 42.937

Review 4.  Glioma EVs Contribute to Immune Privilege in the Brain.

Authors:  Erik R Abels; Marike L D Broekman; Xandra O Breakefield; Sybren L N Maas
Journal:  Trends Cancer       Date:  2019-06-04

5.  Targeted therapy for high-grade glioma with the TGF-β2 inhibitor trabedersen: results of a randomized and controlled phase IIb study.

Authors:  U Bogdahn; P Hau; G Stockhammer; N K Venkataramana; A K Mahapatra; A Suri; A Balasubramaniam; S Nair; V Oliushine; V Parfenov; I Poverennova; M Zaaroor; P Jachimczak; S Ludwig; S Schmaus; H Heinrichs; K-H Schlingensiepen
Journal:  Neuro Oncol       Date:  2010-10-27       Impact factor: 12.300

6.  Glioblastoma cells inhibit astrocytic p53-expression favoring cancer malignancy.

Authors:  D Biasoli; M F Sobrinho; A C C da Fonseca; D G de Matos; L Romão; R de Moraes Maciel; S K Rehen; V Moura-Neto; H L Borges; F R S Lima
Journal:  Oncogenesis       Date:  2014-10-20       Impact factor: 7.485

Review 7.  Tunneling Nanotubes and Gap Junctions-Their Role in Long-Range Intercellular Communication during Development, Health, and Disease Conditions.

Authors:  Jennifer Ariazi; Andrew Benowitz; Vern De Biasi; Monique L Den Boer; Stephanie Cherqui; Haifeng Cui; Nathalie Douillet; Eliseo A Eugenin; David Favre; Spencer Goodman; Karine Gousset; Dorit Hanein; David I Israel; Shunsuke Kimura; Robert B Kirkpatrick; Nastaran Kuhn; Claire Jeong; Emil Lou; Robbie Mailliard; Stephen Maio; George Okafo; Matthias Osswald; Jennifer Pasquier; Roel Polak; Gabriele Pradel; Bob de Rooij; Peter Schaeffer; Vytenis A Skeberdis; Ian F Smith; Ahmad Tanveer; Niels Volkmann; Zhenhua Wu; Chiara Zurzolo
Journal:  Front Mol Neurosci       Date:  2017-10-17       Impact factor: 6.261

8.  HIF-1α/Wnt signaling-dependent control of gene transcription regulates neuronal differentiation of glioblastoma stem cells.

Authors:  Daniele Boso; Elena Rampazzo; Carlo Zanon; Silvia Bresolin; Francesca Maule; Elena Porcù; Alice Cani; Alessandro Della Puppa; Luca Trentin; Giuseppe Basso; Luca Persano
Journal:  Theranostics       Date:  2019-07-09       Impact factor: 11.556

Review 9.  The Extracellular Matrix and Biocompatible Materials in Glioblastoma Treatment.

Authors:  Andrei Belousov; Sergei Titov; Nikita Shved; Mikhail Garbuz; Grigorii Malykin; Valeriia Gulaia; Alexander Kagansky; Vadim Kumeiko
Journal:  Front Bioeng Biotechnol       Date:  2019-11-19

Review 10.  Tumor microenvironment complexity and therapeutic implications at a glance.

Authors:  Roghayyeh Baghban; Leila Roshangar; Rana Jahanban-Esfahlan; Khaled Seidi; Abbas Ebrahimi-Kalan; Mehdi Jaymand; Saeed Kolahian; Tahereh Javaheri; Peyman Zare
Journal:  Cell Commun Signal       Date:  2020-04-07       Impact factor: 5.712

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  1 in total

1.  Isolinderalactone inhibits glioblastoma cell supernatant-induced angiogenesis.

Authors:  Seo-Yeon Lee; Jung Hwa Park; Kang-Hyun Cho; Huiseon Kim; Hwa Kyoung Shin
Journal:  Oncol Lett       Date:  2022-08-02       Impact factor: 3.111

  1 in total

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