| Vol. 14.45 – 24 November, 2023 |
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| Scientists performed a multi-omics time course analysis of a pan-small cell neuroendocrine cancer model, a forward genetic transformation using human prostate basal cells and identified a shared developmental, arc-like, and entropy-high trajectory among all transformation model replicates. [Cancer Cell] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| Knocking down SND1 in human prostate epithelial cells, especially those overexpressing ERG, negatively impacted cell proliferation. [Nature Communications] |
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| The authors demonstrated that SMYD3 critically regulated tumor-associated phenotypes via its methyltransferase activity in prostate cancer cells and mouse xenograft models. [Science Advances] |
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| Using single-cell RNA sequencing of primary prostate epithelial cultures, scientists elucidated organ-specific, zone-specific, and cluster-specific gene expression differences in basal cells isolated from human prostate and seminal vesicle. [Journal Of Pathology] |
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| Investigators demonstrated that insulin like growth factor 1 was necessary for the generation of benign prostatic hyperplasia-1 cell spheroids and patient-derived benign prostatic hyperplasia cell organoids in three-dimensional culture. [JCI Insight] |
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| The authors developed a multiplex in situ method to spatially quantify cell type specific mitochondrial DNA copy number, and showed that it was increased in luminal cells of high-grade prostatic intraepithelial neoplasia and in prostatic adenocarcinomas, and was further elevated in metastatic castration-resistant prostate cancer. [JCI Insight] |
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| Researchers investigated the role of diacylglycerol acyltransferases 1 (DGAT1) and its potential effects on cellular energy homeostasis and autophagy flux in prostate cancer. [Oncogene] |
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| Copper, sulfur, nitrogen–carbon quantum dot nanoparticles loaded with the chemotherapy drug disulfiram were tested on the prostate cancer cell line PC3. [Nanomedicine] |
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| Investigators identified that chemokine receptor CXCR4 bound to PI4KIIIα adaptor proteins TTC7 and this interaction induced plasma membrane PI4P production in prostate cancer cells. [Scientific Reports] |
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| The authors highlight therapeutic nanoparticles as a solution for prostate cancer chemotherapy, exploring targeting strategies and approaches to combat drug resistance. [Cancer Treatment and Research Communications] |
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| Professor Gail Risbridger and her research team from Monash University will receive $5 million in funding over 5 years for research to advance immunotherapy treatments for treating prostate cancer. [NHMRC] |
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| January 16 – 19, 2024 San Diego, California, United States & Virtual |
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| The University of Texas MD Anderson Cancer Center – Houston, Texas, United States |
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| Babraham Institute – Cambridge, England, United Kingdom |
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| Cedars-Sinai – Los Angeles, California, United States |
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| Fred Hutchinson Cancer Center – Seattle, Washington, United States |
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| University of Southern California – Los Angeles, California, United States |
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