BET proteins: Biological functions and therapeutic interventions

J Guo, Q Zheng, Y Peng - Pharmacology & Therapeutics, 2023 - Elsevier
Bromodomain and extra-terminal (BET) family member proteins (BRD2, BRD3, BRD4 and
BRDT) play a pivotal role in interpreting the epigenetic information of histone Kac …

[HTML][HTML] Anti-androgen receptor therapies in prostate cancer: a brief update and perspective

J Huang, B Lin, B Li - Frontiers in oncology, 2022 - frontiersin.org
Prostate cancer is a major health issue in western countries and is the second leading
cause of cancer death in American men. Prostate cancer depends on the androgen receptor …

ASCL1 activates neuronal stem cell-like lineage programming through remodeling of the chromatin landscape in prostate cancer

S Nouruzi, D Ganguli, N Tabrizian, M Kobelev… - Nature …, 2022 - nature.com
Abstract Treatment with androgen receptor pathway inhibitors (ARPIs) in prostate cancer
leads to the emergence of resistant tumors characterized by lineage plasticity and …

Transcriptional profiling of matched patient biopsies clarifies molecular determinants of enzalutamide-induced lineage plasticity

TC Westbrook, X Guan, E Rodansky, D Flores… - Nature …, 2022 - nature.com
The androgen receptor (AR) signaling inhibitor enzalutamide (enza) is one of the principal
treatments for metastatic castration-resistant prostate cancer (CRPC). Several emergent …

[HTML][HTML] The role of epigenetic change in therapy-induced neuroendocrine prostate cancer lineage plasticity

WK Storck, AM May, TC Westbrook, Z Duan… - Frontiers in …, 2022 - frontiersin.org
The androgen receptor (AR) signaling pathway is critical for growth and differentiation of
prostate cancer cells. For that reason, androgen deprivation therapy with medical or surgical …

Exploring anti-androgen therapies in hormone dependent prostate cancer and new therapeutic routes for castration resistant prostate cancer

AE Harris, VM Metzler, J Lothion-Roy… - Frontiers in …, 2022 - frontiersin.org
Androgen deprivation therapies (ADTs) are important treatments which inhibit androgen-
induced prostate cancer (PCa) progression by either preventing androgen biosynthesis (eg …

[HTML][HTML] Improving anti-tumor efficacy of low-dose Vincristine in rhabdomyosarcoma via the combination therapy with FOXM1 inhibitor RCM1

J Donovan, Z Deng, F Bian, S Shukla… - Frontiers in …, 2023 - frontiersin.org
Rhabdomyosarcoma (RMS) is a highly metastatic soft-tissue sarcoma that often develops
resistance to current therapies, including vincristine. Since the existing treatments have not …

[HTML][HTML] From Therapy Resistance to targeted therapies in prostate Cancer

F Moreira-Silva, R Henrique, C Jerónimo - Frontiers in Oncology, 2022 - frontiersin.org
Prostate cancer (PCa) is the second most common malignancy among men worldwide.
Although early-stage disease is curable, advanced stage PCa is mostly incurable and …

[HTML][HTML] LSD1 promotes prostate cancer reprogramming by repressing TP53 signaling independently of its demethylase function

A Kumaraswamy, Z Duan, D Flores, C Zhang… - JCI insight, 2023 - ncbi.nlm.nih.gov
Abstract Lysine-specific demethylase 1 (LSD1) is a histone demethylase that promotes
stemness and cell survival in cancers such as prostate cancer. Most prostate malignancies …

Addressing the need for more therapeutic options in neuroendocrine prostate cancer

J Kemble, ED Kwon, RJ Karnes - Expert review of anticancer …, 2023 - Taylor & Francis
Introduction Neuroendocrine prostate cancer (NEPC) is an aggressive form of prostate
cancer frequently seen after prolonged treatment of castration resistant prostate cancer …