Literature DB >> 29199023

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.

Sandy T Liu1, Gavin Hui2, Colleen Mathis3, Karim Chamie4, Allan J Pantuck4, Alexandra Drakaki5.   

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.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Bladder cancer; Inhibitors; PI3K; Targeted therapy; mTOR

Mesh:

Substances:

Year:  2017        PMID: 29199023     DOI: 10.1016/j.clgc.2017.10.011

Source DB:  PubMed          Journal:  Clin Genitourin Cancer        ISSN: 1558-7673            Impact factor:   2.872


  23 in total

1.  Rapamycin Prevents Surgery-Induced Immune Dysfunction in Patients with Bladder Cancer.

Authors:  Robert S Svatek; Niannian Ji; Essel de Leon; Neelam Z Mukherjee; Aashish Kabra; Vincent Hurez; Marlo Nicolas; Joel E Michalek; Martin Javors; Karen Wheeler; Z Dave Sharp; Carolina B Livi; Zhen-Ju Shu; David Henkes; Tyler J Curiel
Journal:  Cancer Immunol Res       Date:  2018-12-18       Impact factor: 11.151

Review 2.  Emerging biomarkers and targeted therapies in urothelial carcinoma.

Authors:  Prateek Mendiratta; Petros Grivas
Journal:  Ann Transl Med       Date:  2018-06

Review 3.  RETRACTED ARTICLE: Roles of the PI3K/AKT/mTOR signalling pathways in neurodegenerative diseases and tumours.

Authors:  Fei Xu; Lixin Na; Yanfei Li; Linjun Chen
Journal:  Cell Biosci       Date:  2020-04-01       Impact factor: 7.133

4.  Cucurbitacin B and cisplatin induce the cell death pathways in MB49 mouse bladder cancer model.

Authors:  Yener Kurman; Ilker Kiliccioglu; Asiye U Dikmen; Guldal Esendagli; Cenk Y Bilen; Sinan Sozen; Ece Konac
Journal:  Exp Biol Med (Maywood)       Date:  2020-04-06

5.  Downregulation of PTCD1 in Bladder Urothelial Carcinoma Predicts Poor Prognosis and Levels of Immune Infiltration.

Authors:  Zhongbao Zhou; Yongjian Zhou; Xin Zhou; Yongjin Huang; Yuanshan Cui; Yong Zhang
Journal:  J Oncol       Date:  2022-06-28       Impact factor: 4.501

6.  Synergistic Effects of Combination Therapy with AKT and mTOR Inhibitors on Bladder Cancer Cells.

Authors:  Hyera Kim; Su Jin Lee; In Kyoung Lee; Suejean C Min; Hyun Hwan Sung; Byong Chang Jeong; Jeeyun Lee; Se Hoon Park
Journal:  Int J Mol Sci       Date:  2020-04-18       Impact factor: 5.923

Review 7.  Sulforaphane Impact on Reactive Oxygen Species (ROS) in Bladder Carcinoma.

Authors:  Hui Xie; Felix K-H Chun; Jochen Rutz; Roman A Blaheta
Journal:  Int J Mol Sci       Date:  2021-05-31       Impact factor: 5.923

8.  Chronic Sulforaphane Administration Inhibits Resistance to the mTOR-Inhibitor Everolimus in Bladder Cancer Cells.

Authors:  Saira Justin; Jochen Rutz; Sebastian Maxeiner; Felix K-H Chun; Eva Juengel; Roman A Blaheta
Journal:  Int J Mol Sci       Date:  2020-06-04       Impact factor: 5.923

Review 9.  Curcumin-A Viable Agent for Better Bladder Cancer Treatment.

Authors:  Jochen Rutz; Andrea Janicova; Katja Woidacki; Felix K-H Chun; Roman A Blaheta; Borna Relja
Journal:  Int J Mol Sci       Date:  2020-05-26       Impact factor: 5.923

Review 10.  Putting the Brakes on Tumorigenesis with Natural Products of Plant Origin: Insights into the Molecular Mechanisms of Actions and Immune Targets for Bladder Cancer Treatment.

Authors:  Qiushuang Wu; Janet P C Wong; Hang Fai Kwok
Journal:  Cells       Date:  2020-05-13       Impact factor: 6.600

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