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

Authors :
Antonino Glaviano
Aaron S. C. Foo
Hiu Y. Lam
Kenneth C. H. Yap
William Jacot
Robert H. Jones
Huiyan Eng
Madhumathy G. Nair
Pooyan Makvandi
Birgit Geoerger
Matthew H. Kulke
Richard D. Baird
Jyothi S. Prabhu
Daniela Carbone
Camilla Pecoraro
Daniel B. L. Teh
Gautam Sethi
Vincenzo Cavalieri
Kevin H. Lin
Nathalie R. Javidi-Sharifi
Eneda Toska
Matthew S. Davids
Jennifer R. Brown
Patrizia Diana
Justin Stebbing
David A. Fruman
Alan P. Kumar
Source :
Molecular Cancer, Vol 22, Iss 1, Pp 1-37 (2023)
Publication Year :
2023
Publisher :
BMC, 2023.

Abstract

Abstract 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.

Details

Language :
English
ISSN :
14764598
Volume :
22
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Molecular Cancer
Publication Type :
Academic Journal
Accession number :
edsdoj.9b643e4724194798a585634205af8fef
Document Type :
article
Full Text :
https://doi.org/10.1186/s12943-023-01827-6