| Vol. 13.11 – 25 March, 2022 |
| |
|
|
| miR-346 could be particularly effective as a therapeutic in the context of decreased NORAD observed in advanced prostate cancer, and in transcriptionally-hyperactive cancer cells. [Molecular Cancer] |
| |
|
|
PUBLICATIONSRanked by the impact factor of the journal |
|
|
|
| Comprehensive mapping of the mTOR chromatin-bound interactome in both androgen-dependent and -independent cellular models of prostate cancer identified a conserved 67-protein interaction network enriched for chromatin modifiers, transcription factors, and SUMOylation machinery. [Cell Reports] |
|
|
|
| Scientists detected that the loss of the androgen-responsive transcription factor, zinc finger, and BTB domain containing 10 (ZBTB10), could activate pyruvate kinase L/R to enhance a neuroendocrine differentiation response that was associated with glucose uptake by prostate cancer cells. [Cell Death & Disease] |
|
|
|
| Researchers reported that autophagy affected differently the response of prostate cancer cell lines to olaparib depending on its activation status. [Communications Biology] |
|
|
|
| In vitro and in vivo data provided new insights for understanding the mechanisms underlying high-dose-dihydrotestosterone suppression of the enzalutamide-resistant CRPC cell growth, supporting a potential therapy using high-dose-androgens to suppress CRPC progression in the future. [Cell Death Discovery] |
|
|
|
| The authors assessed the function of KMT2C in prostate cancer cell proliferation, colony formation, and migration. [Journal of Cancer Research and Clinical Oncology] |
|
|
|
| Researchers investigated the use of designed ankyrin repeat protein Ec1 for targeted delivery of Pseudomonas exotoxin A variant (LoPE) with low immunogenicity and low non‑specific toxicity to epithelial cell adhesion molecule‑expressing prostate cancer cells. [Oncology Reports] |
|
|
|
| Investigators analyzed the carcinogenetic potential of exposure to GHRH of a nontumor human prostate epithelial cell line (RWPE-1) as well as its transforming effect in a xenograft model. [Prostate] |
|
|
|
| Through co-targeting the androgen receptor (AR) signaling, Diptoindonesin G robustly improved the efficacy of HSP90 inhibitors and enzalutamide in both human prostate cancer cells and in vivo xenograft mouse model. [Prostate] |
|
|
|
| Scientists investigated whether the novel factor 3,5-dihydroxy-4-methoxybenzyl alcohol suppressed the activity of metastatic human prostate cancer PC-3 or DU-145 cells. [Anti-Cancer Drugs] |
| |
|
|
|
| The authors provide a mechanistic discussion of autophagy in prostate cancer. [Journal of Experimental & Clinical Cancer Research] |
|
|
|
| Scientists discuss the advancement of PCSK9 research on its role and underlying mechanisms in tumor development and progression. [Naunyn-Schmiedebergs Archives of Pharmacology] |
|
|
|
|
| Novartis announced today that the US FDA approved PluvictoTM for the treatment of adult patients with a certain type of advanced cancer called prostate-specific membrane antigen–positive metastatic CRPC that has spread to other parts of the body. [Novartis Pharma AG] |
|
|
|
|
| May 25 – 29, 2022 Lyon, France |
|
|
|
|
|
| CRUK Manchester Institute – Manchester, United Kingdom |
|
|
|
| University of Southern Denmark – Odense M, Denmark |
|
|
|
| Dana-Farber Cancer Institute – Boston, Massachusetts, United States |
|
|
|
| The University of British Columbia – Vancouver, British Columbia, Canada |
|
|
|
| Singapore-MIT Alliance for Research and Technology (SMART) Centre – Singapore, Singapore |
|
|
|
|