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The mTOR pathway in Gliomas: From molecular insights to targeted therapies
Safura Pournajaf1, Mohammad Hossein Pourgholami2
1Hearing Disorders Research Center, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Abstract:
Glioblastoma multiforme (GBM) is the most prevalent primary brain tumor with extreme aggressiveness, poor prognosis, and a high mortality rate. To maintain a high rate of proliferation and invasion, GBM cells manipulate many biological processes within the cell and the tumor microenvironment, including intracellular signaling pathways. One of the main signaling pathways with proven roles in GBM pathology is the PI3K/AKT/mTOR signaling pathway, with its molecular alterations considered a hallmark of GBM. Through integrating with various upstream signals from growth factors, nutrients, and energy status, regulatory feedback mechanisms with other signaling pathways, manipulation of glioma stem cells, and epigenetic regulations, this pathway contributes to GBM cell proliferation, growth, angiogenesis, and metastasis, and more importantly escape the effects of available therapies. The extent of involvement of the PI3K/AKT/mTOR signaling pathway grants a more delicate and detailed understanding of this pathway. This review provides a deep insight into the mTOR pathway in GBM, revealing its modulators and interactions with upstream and downstream regulators. It also provides comprehensive information on the latest mTOR-targeted therapies and resistance mechanisms.
Insights
Glioblastoma multiforme (GBM) cells exploit the PI3K/AKT/mTOR pathway for aggressive growth and therapy evasion. Understanding this pathway
Area of Science:
- Oncology
- Molecular Biology
- Cancer Signaling
Background:
- Glioblastoma multiforme (GBM) is an aggressive primary brain tumor with poor prognosis.
- GBM cells manipulate intracellular signaling pathways, including PI3K/AKT/mTOR, for proliferation and invasion.
Purpose of the Study:
- To provide a detailed review of the mTOR pathway's role in GBM.
- To elucidate mTOR's modulators, upstream/downstream regulators, and interactions.
Main Methods:
- Literature review of the PI3K/AKT/mTOR signaling pathway in GBM.
- Analysis of mTOR's involvement in GBM cell biology and therapeutic resistance.
Main Results:
- Molecular alterations in the PI3K/AKT/mTOR pathway are a hallmark of GBM.
- This pathway drives GBM cell proliferation, angiogenesis, metastasis, and therapy escape.
Conclusions:
- The PI3K/AKT/mTOR pathway is critical for GBM pathogenesis.
- Understanding mTOR signaling is key for developing effective GBM therapies and overcoming resistance.
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