Signaling pathways and therapeutic approaches in glioblastoma multiforme (Review)

Marsel Khabibov, Airat Garifullin*, Yanis Boumber*, Karam Khaddour, Manuel Fernandez, Firat Khamitov, Larisa Khalikova, Natalia Kuznetsova, Oleg Kit, Leonid Kharin

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

64 Scopus citations

Abstract

Glioblastoma multiforme (GBM) is the most aggres- sive type of primary brain tumor and is associated with a poor clinical prognosis. Despite the progress in the understanding of the molecular and genetic changes that promote tumorigenesis, effec- tive treatment options are limited. The present review intended to identify and summarize major signaling pathways and genetic abnormalities involved in the pathogenesis of GBM, as well as therapies that target these pathways. Glioblastoma remains a diffi- cult to treat tumor; however, in the last two decades, significant improvements in the understanding of GBM biology have enabled advances in available therapeutics. Significant genomic events and signaling pathway disruptions (NF-κB, Wnt, PI3K/AKT/mTOR) involved in the formation of GBM were discussed. Current therapeutic options may only marginally prolong survival and the current standard of therapy cures only a small fraction of patients. As a result, there is an unmet requirement for further study into the processes of glioblastoma pathogenesis and the discovery of novel therapeutic targets in novel signaling pathways implicated in the evolution of glioblastoma.

Original languageEnglish (US)
Article number69
JournalInternational journal of oncology
Volume60
Issue number6
DOIs
StatePublished - Jun 2022

Funding

YB was supported in part by the NIH R01 CA218802 grant, Jimmy V Foundation T2018-013 Translational Award grant, Northwestern University 2022 Translational Bridge Award and by the NCI NIH Core Grant P30 CA060553 to the Robert H. Lurie Comprehensive Cancer Center at Northwestern University (Chicago, USA). This study was also partially supported by the Russian government program for Competitive Growth of the Kazan Federal University (Kazan, Russia) and Northwestern University (Chicago, USA) start-up funds to YB. YB was supported in part by the NIH R01 CA218802 grant, Jimmy V Foundation T2018‑013 Translational Award grant, Northwestern University 2022 Translational Bridge Award and by the NCI NIH Core Grant P30 CA060553 to the Robert H. Lurie Comprehensive Cancer Center at Northwestern University (Chicago, USA). This study was also partially supported by the Russian government program for Competitive Growth of the Kazan Federal University (Kazan, Russia) and Northwestern University (Chicago, USA) start‑up funds to YB.

Keywords

  • glioblastoma
  • immunotherapy
  • mutations
  • signaling pathways
  • targeted therapy
  • tumor treating fields

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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