PI3K/AKT/mTOR signaling transduction pathway and targeted therapies in cancer

Сигнальный путь PI3K/AKT/mTOR и таргетная терапия рака
Kevin Lin, Jennifer R. Brown, Aaron Song Chuan Foo, Alan Prem Kumar, Daniel Boon Loong Teh, Robert H. Jones, Birgit Geoerger, Pooyan Makvandi, Gautam Sethi, Antonino Glaviano, William Jacot, Matthew S. Davids, Matthew H. Kulke, David A. Fruman, Justin Stebbing, Nathalie Javidi‐Sharifi, Hiu Yan Lam, Kenneth Chun-Yong Yap, Huiyan Eng, Madhumathy G Nair, Richard D. Baird, Jyothi S. Prabhu, Daniela Carbone, Camilla Pecoraro, Vincenzo Cavalieri, Eneda Toska, Patrizia Diana
2023-08-18

Cancer therapy resistancePI3K AKT mTOR inhibitorsPI3K/AKT/mTOR signaling pathwayPTEN loss of functionTargeted immunotherapy
The PI3K/AKT/mTOR (PAM) signaling pathway is a highly conserved signal transduction network in eukaryotic cells that promotes cell survival, cell growth, and cell cycle progression. Growth factor signalling to transcription factors in the PAM axis is highly regulated by multiple cross-interactions with several other signaling pathways, and dysregulation of signal transduction can predispose to cancer development. The PAM axis is the most frequently activated signaling pathway in human cancer and is often implicated in resistance to anticancer therapies. Dysfunction of components of this pathway such as hyperactivity of PI3K, loss of function of PTEN, and gain-of-function of AKT, are notorious drivers of treatment resistance and disease progression in cancer. In this review we highlight the major dysregulations in the PAM signaling pathway in cancer, and discuss the results of PI3K, AKT and mTOR inhibitors as monotherapy and in co-administation with other antineoplastic agents in clinical trials as a strategy for overcoming treatment resistance. Finally, the major mechanisms of resistance to PAM signaling targeted therapies, including PAM signaling in immunology and immunotherapies are also discussed.
1
Clinical studies have evaluated PI3K, AKT, and mTOR inhibitors as monotherapies and in combination with other anticancer agents to overcome therapeutic resistance.
2
PI3K hyperactivation, PTEN loss of function, and AKT gain of function drive cancer progression and treatment resistance.
3
PI3K/AKT/mTOR signaling is the most frequently activated pathway in human cancer and is commonly associated with resistance to anticancer therapies.
4
Resistance mechanisms to PI3K/AKT/mTOR-targeted therapies, including interactions with immune signaling and immunotherapies, represent major challenges.
5
The PI3K/AKT/mTOR pathway regulates cell survival, growth, and cell-cycle progression through a highly conserved signaling network.

PI3K/AKT/mTOR (PAM) signaling pathway in human cancer

Dysregulation of the PAM pathway, its role in cancer progression and treatment resistance, and the efficacy and resistance mechanisms of PI3K, AKT, and mTOR targeted therapies

Publication Details
Publication Date
2023-08-18
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Authors
Kevin Lin
Jennifer R. Brown
Aaron Song Chuan Foo
Alan Prem Kumar
Daniel Boon Loong Teh
Robert H. Jones
Birgit Geoerger
Pooyan Makvandi
Gautam Sethi
Antonino Glaviano
William Jacot
Matthew S. Davids
Matthew H. Kulke
David A. Fruman
Justin Stebbing
Nathalie Javidi‐Sharifi
Hiu Yan Lam
Kenneth Chun-Yong Yap
Huiyan Eng
Madhumathy G Nair
Richard D. Baird
Jyothi S. Prabhu
Daniela Carbone
Camilla Pecoraro
Vincenzo Cavalieri
Eneda Toska
Patrizia Diana
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