Newsletters
A Ligandable PNT Domain Establishes ERG As a Directly Targetable Oncogenic Driver in Prostate Cancer
[Proceedings of the National Academy of Sciences of the United States of America] Investigators demonstrated continued dependency on ERG in metastatic prostate cancer and identify a druggable pocket within its N-terminal Pointed (PNT) domain.
ZNF263-NuRD-Mediated Repression of STAT1 Curtails MHC-I Antigen Presentation and IFN-γ Efficacy in Prostate Cancer
[Proceedings of the National Academy of Sciences of the United States of America] Researchers identified ZNF263 as a transcriptional repressor that silences MHC-I by recruiting nucleosome-remodeling and deacetylase (NuRD) to the STAT1 promoter, reducing STAT1 and MHC-I expression.
Randomized Phase II Trial of Nivolumab and Ipilimumab with or without Stereotactic Body Radiation Therapy in Patients with Metastatic Castration-Resistant Prostate Cancer: The CheckPRO,...
[Journal for Immunotherapy of Cancer] Scientists hypothesized that the addition of stereotactic body radiation therapy could enhance immune responses and improve treatment outcomes.
A Novel lncRNA HUDRPC Suppresses Ferroptosis via the DDX5/DDIT3 Pathway to Promote Docetaxel Resistance in Prostate Cancer
[Cancer Letters] The authors functionally characterized a novel docetaxel resistance-associated lncRNA in prostate cancer. They identified an uncharacterized lncRNA, termed HUDRPC, which was significantly upregulated in resistant cells and patient-derived tumor tissues.
Adipose Triglyceride Lipase Driven Lipolysis As a Targetable Metabolic Vulnerability in Prostate Cancer with Intrinsic Metabolic Inflexibility
[British Journal of Cancer] ATGL-mediated lipolysis represents a promising therapeutic target in prostate cancer, with heightened sensitivity in tumours lacking metabolic flexibility to utilize alternative pathways.
METTL5-Mediated rRNA Modification Controls Prostate Cancer Progression through the IRF7/DNA2 Axis and Mitophagy Regulation
[Oncogene] Researchers showed that the rRNA m6A methyltransferase METTL5 was progressively upregulated during prostate cancer progression and was associated with poor patient survival.
Targeting the NR3C1-ACSL4 Axis Triggers Ferroptosis to Overcome Radioresistance in Prostate Cancer
[Cancer Science] Scientists revealed that the nuclear receptor subfamily 3 group C member 1 (NR3C1)-acyl-CoA synthetase long-chain family member 4 (ACSL4) axis regulates lipid peroxidation and promotes radioresistance.
Development and Advantages of O-(Carboxymethyl)-L-Tyrosine-Based PSMA-Targeting Theranostics for Prostate Cancer
[Journal of Medicinal Chemistry] The authors highlight that PSMA-targeting agents incorporate the O-(carboxymethyl)-L-tyrosine scaffold, a versatile linker that enhances binding affinity and optimizes pharmacokinetics.
FDA Grants Priority Review for Pfizer’s TALZENNA Plus XTANDI for the Treatment of Metastatic Prostate Cancer
[Pfizer, Inc.] Pfizer, Inc. announced that the US FDA accepted for Priority Review a supplemental New Drug Application for TALZENNA®, an oral poly ADP-ribose polymerase inhibitor, in combination with XTANDI®, an androgen receptor pathway inhibitor, in men with homologous recombination repair gene-altered metastatic castration-sensitive prostate cancer, also known as metastatic hormone-sensitive prostate cancer.
Oncogenic snoRNA SNORD78 Fuels Colorectal Cancer by Protecting the m6a Reader IMP2 to Enhance Phospholipid Metabolism
[Proceedings of the National Academy of Sciences of the United States of America] The authors systematically deciphered the precise interaction mechanism between SNORD78 and the m6A reader IMP2 in colorectal cancer.
DCAF13: A Positive Regulator of Colon Cancer Cell Proliferation via the AMER2/ Wnt/β-Catenin Pathway
[NPJ Precision Oncology] As one of the Cullin RING Ligase 4 adapters, DNA damage-binding protein 1 - and CUL4 correlation factor 13 (DCAF13) appeared strongly expressed in different tumors. Scientists' findings confirm enhanced expression of DCAF13 in tissues of colorectal cance origin and related cell.
Matrix Stiffness Promotes Colorectal Cancer Progression via Golgi-Dependent Cholesterol Synthesis
[Cell Death & Disease] Researchers showed that extracellular matrix stiffness drives colorectal cancer progression by activating Piezo1-dependent cholesterol synthesis.

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