PI3K‑AKT‑mTOR signaling in prostate cancer progression and androgen deprivation therapy resistance - Full Text Article

Prostate cancer (PCa) is the second most common malignancy among men in the world. Castration-resistant prostate cancer (CRPC) is the lethal form of the disease, which develops upon resistance to first line androgen deprivation therapy (ADT). Emerging evidence demonstrates a key role for the PI3K-AKT-mTOR signaling axis in the development and maintenance of CRPC. aju logoThis pathway, which is deregulated in the majority of advanced PCas, serves as a critical nexus for the integration of growth signals with downstream cellular processes such as protein synthesis, proliferation, survival, metabolism and differentiation, thus providing mechanisms for cancer cells to overcome the stress associated with androgen deprivation. Furthermore, preclinical studies have elucidated a direct connection between the PI3K-AKT-mTOR and androgen receptor (AR) signaling axes, revealing a dynamic interplay between these pathways during the development of ADT resistance. Thus, there is a clear rationale for the continued clinical development of a number of novel inhibitors of the PI3K pathway, which offer the potential of blocking CRPC growth and survival. In this review, we will explore the relevance of the PI3K-AKT-mTOR pathway in PCa progression and castration resistance in order to inform the clinical development of specific pathway inhibitors in advanced PCa. In addition, we will highlight current deficiencies in our clinical knowledge, most notably the need for biomarkers that can accurately predict for response to PI3K pathway inhibitors.


View full text article:


Written by:
Merritt P Edlind,1 and Andrew C Hsieh2  Are you the author?
1Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA
2Division of Hematology/Oncology and Department of Internal Medicine, University of California, San Francisco, CA, USA.

Reference: Asian J Androl. 2014 May-Jun;16(3):378-86
doi: 10.4103/1008-682X.122876

PubMed Abstract
PMID: 24759575