| Vol. 13.15 – 29 April, 2022 |
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| HOXB13 loss or G84E mutation led to lipid accumulation in prostate cancer cells, thereby promoting cell motility and xenograft tumor metastasis, which was mitigated by pharmaceutical inhibition of fatty acid synthase. [Nature Genetics] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| MYCi975 synergistically sensitized resistant prostate cancer cells to enzalutamide and estrogen receptor–positive breast cancer cells to 4-hydroxytamoxifen. [Science Advances] |
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| Scientists provided insights into the epigenetic alterations induced by androgen receptor pathway inhibitors (ARPIs), governed by ASCL1, provided a proof of principle of targeting ASCL1 to reverse neuroendocrine phenotype, supported luminal conversion and re-addiction to ARPIs. [Nature Communications] |
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| Researchers comprehensively characterized phased genomic alterations in the commonly used prostate cancer cell lines, providing a useful resource for future prostate cancer research. [Molecular Cancer Research] |
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| Investigators concluded that inhibition of G9a methyltransferase activity by CM-272 has anti-tumor effect in prostate cancer cells, holding therapeutic potential against CRPC. [Biomedicine & Pharmacotherapy] |
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| The presence of an androgen synthesis, independent of CYP17A1 activity, has been shown to exist in prostate cancer cells, and therefore, novel androgen synthesis inhibitors were needed for the treatment of enzalutamide-resistant CRPC tumors that did not respond to abiraterone. [iScience] |
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| Silencing ELF3 in both benign prostate and prostate cancer cell lines resulted in decreased colony forming ability, inhibition of cell migration and reduced cell viability due to cell cycle arrest, establishing ELF3 as a cell cycle regulator. [Febs Open Bio] |
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| Normal peripheral blood specimens spiked with cultured breast and prostate cancer cells and 47 clinical samples were used to validate assay performance. [American Journal of Clinical Pathology] |
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| VGRNb-DT demonstrated a successful bioconjugation and variable concentrations were correlated with cell death in prostate cancer PC-3 cells. [Molecular Biotechnology] |
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| The authors review the pathological and immunomodulatory roles of P2Y purinergic nucleotide receptors in prostate cancer and their potential as therapeutic targets to address some of the clinical limitations in prostate cancer treatment. [Biochimica et Biophysica Acta-Reviews On Cancer] |
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| Future studies are needed to verify the clinical usefulness of Proclarix in men with suspected prostate cancer before and after multiparametric MRI. [Molecular Diagnosis & Therapy] |
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| POINT Biopharma Global, Inc. announced the first patient in the European Union has been dosed in the Phase III SPLASH trial investigating the use of 177Lu-PNT2002, a PSMA-targeted radioligand, in pre-chemotherapy metastatic CRPC. [POINT Biopharma Global, Inc.] |
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| September 19 – 20, 2022 Vejle, Denmark |
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| University of Texas MD Anderson Cancer Center – Houston, Texas, United States |
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| University Hospital Frankfurt – Frankfurt, Germany |
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| City of Hope – Duarte, California, United States |
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| Washington State University – Spokane, Washington, United States |
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| Dana-Farber Cancer Institute – Boston, Massachusetts, United States |
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