The Current Status and Future Role of the Phosphoinositide 3 Kinase/AKT Signaling Pathway in Urothelial Cancer: An Old Pathway in the New Immunotherapy Era
- PMID: 29199023
- DOI: 10.1016/j.clgc.2017.10.011
The Current Status and Future Role of the Phosphoinositide 3 Kinase/AKT Signaling Pathway in Urothelial Cancer: An Old Pathway in the New Immunotherapy Era
Abstract
The phosphoinositide 3 kinase (PI3K)/protein kinase B (AKT)/mammalian target of rapamycin (mTOR) pathway is a well studied signaling pathway that regulates diverse cellular functions including proliferation, metabolism, and transcription. Aberrant activation of this pathway has been implicated in multiple cancers. Genomic studies have shown that activating mutations in oncogenes as well as inactivating mutations in tumor suppressor genes are present across a variety of malignancies, including urothelial carcinoma. In bladder cancer, up to 40% of tumors exhibit constitutive activation of the PI3K/AKT/mTOR pathway. Current treatments for non-muscle-invasive disease confer a 5-year cancer-specific survival rate as high as 90%. However, patients with muscle-invasive, recurrent, or metastatic disease have a poor prognosis. Although the introduction of immune checkpoint inhibitors is certainly changing the therapeutic landscape and is a great addition to the platinum-based therapy that was the standard of care for the past 3 decades, it is anticipated that a great number of patients would fail to respond or their disease would progress with either chemotherapy or immunotherapy. Therefore, the use of agents that target members of the PI3K/AKT/mTOR pathway represent an attractive, alternative therapeutic strategy for patients with advanced urothelial carcinoma. In this review we describe the pathway, with a focus on the rationale for targeting the PI3K/AKT/mTOR pathway in patients with advanced urothelial carcinoma and considers the challenges that we face from the current clinical trials. Novel agents such as PI3K inhibitors and microRNA inhibitors that target this pathway might lead to durable responses especially when used in combination with chemotherapy or immune checkpoint inhibitors, however, toxicity remains an obstacle. Finally, in this review we discuss the importance of developing biomarkers to help select appropriate patients and identify optimal treatment options.
Keywords: Bladder cancer; Inhibitors; PI3K; Targeted therapy; mTOR.
Copyright © 2017 Elsevier Inc. All rights reserved.
Similar articles
-
A comprehensive immunohistochemical and molecular approach to the PI3K/AKT/mTOR (phosphoinositide 3-kinase/v-akt murine thymoma viral oncogene/mammalian target of rapamycin) pathway in bladder urothelial carcinoma.BJU Int. 2012 Dec;110(11 Pt C):E1237-48. doi: 10.1111/j.1464-410X.2012.11569.x. Epub 2012 Oct 29. BJU Int. 2012. PMID: 23107319
-
Molecular targets for cancer therapy in the PI3K/AKT/mTOR pathway.Pharmacol Ther. 2014 May;142(2):164-75. doi: 10.1016/j.pharmthera.2013.12.004. Epub 2013 Dec 9. Pharmacol Ther. 2014. PMID: 24333502 Review.
-
Emerging therapeutic targets in bladder cancer.Cancer Treat Rev. 2015 Feb;41(2):170-8. doi: 10.1016/j.ctrv.2014.11.003. Epub 2014 Nov 24. Cancer Treat Rev. 2015. PMID: 25498841 Review.
-
Targeting the PI3K/AKT/mTOR Pathway in Bladder Cancer.Methods Mol Biol. 2018;1655:335-350. doi: 10.1007/978-1-4939-7234-0_23. Methods Mol Biol. 2018. PMID: 28889395 Review.
-
Targeting the phosphatidylinositol 3-kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR) pathway: an emerging treatment strategy for squamous cell lung carcinoma.Cancer Treat Rev. 2014 Sep;40(8):980-9. doi: 10.1016/j.ctrv.2014.06.006. Epub 2014 Jul 3. Cancer Treat Rev. 2014. PMID: 25037117 Review.
Cited by
-
The therapeutic and prognostic implications of molecular biomarkers in urothelial carcinoma.Transl Cancer Res. 2020 Oct;9(10):6609-6623. doi: 10.21037/tcr-20-1243. Transl Cancer Res. 2020. PMID: 35117271 Free PMC article. Review.
-
Urothelial Bladder Carcinomas with High Tumor Mutation Burden Have a Better Prognosis and Targetable Molecular Defects beyond Immunotherapies.Curr Oncol. 2022 Feb 24;29(3):1390-1407. doi: 10.3390/curroncol29030117. Curr Oncol. 2022. PMID: 35323317 Free PMC article.
-
Cucurbitacin B and cisplatin induce the cell death pathways in MB49 mouse bladder cancer model.Exp Biol Med (Maywood). 2020 May;245(9):805-814. doi: 10.1177/1535370220917367. Epub 2020 Apr 6. Exp Biol Med (Maywood). 2020. PMID: 32252554 Free PMC article.
-
Sulforaphane Impact on Reactive Oxygen Species (ROS) in Bladder Carcinoma.Int J Mol Sci. 2021 May 31;22(11):5938. doi: 10.3390/ijms22115938. Int J Mol Sci. 2021. PMID: 34073079 Free PMC article. Review.
-
Synergistic Effects of Combination Therapy with AKT and mTOR Inhibitors on Bladder Cancer Cells.Int J Mol Sci. 2020 Apr 18;21(8):2825. doi: 10.3390/ijms21082825. Int J Mol Sci. 2020. PMID: 32325639 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous