Cellular rewiring in lethal prostate cancer: the architect of drug resistance.
Publication/Presentation Date
5-1-2020
Abstract
Over the past 5 years, the advent of combination therapeutic strategies has substantially reshaped the clinical management of patients with advanced prostate cancer. However, most of these combination regimens were developed empirically and, despite offering survival benefits, are not enough to halt disease progression. Thus, the development of effective therapeutic strategies that target the mechanisms involved in the acquisition of drug resistance and improve clinical trial design are an unmet clinical need. In this context, we hypothesize that the tumour engineers a dynamic response through the process of cellular rewiring, in which it adapts to the therapy used and develops mechanisms of drug resistance via downstream signalling of key regulatory cascades such as the androgen receptor, PI3K-AKT or GATA2-dependent pathways, as well as initiation of biological processes to revert tumour cells to undifferentiated aggressive states via phenotype switching towards a neuroendocrine phenotype or acquisition of stem-like properties. These dynamic responses are specific for each patient and could be responsible for treatment failure despite multi-target approaches. Understanding the common stages of these cellular rewiring mechanisms to gain a new perspective on the molecular underpinnings of drug resistance might help formulate novel combination therapeutic regimens.
Volume
17
Issue
5
First Page
292
Last Page
307
ISSN
1759-4820
Published In/Presented At
Carceles-Cordon, M., Kelly, W. K., Gomella, L., Knudsen, K. E., Rodriguez-Bravo, V., & Domingo-Domenech, J. (2020). Cellular rewiring in lethal prostate cancer: the architect of drug resistance. Nature reviews. Urology, 17(5), 292–307. https://doi.org/10.1038/s41585-020-0298-8
Disciplines
Business Administration, Management, and Operations | Health and Medical Administration | Management Sciences and Quantitative Methods
PubMedID
32203305
Department(s)
Administration and Leadership
Document Type
Article