Prostate Cell News 9.04 February 2, 2018 | |
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TOP STORYResearchers demonstrated that TRIM25 knockdown resulted in p53 downstream activation for cell cycle inhibition and apoptosis induction in LNCaP and 22Rv1 cells. In contrast, overexpression of TRIM25 promoted prostate cancer cell proliferation and inhibited apoptosis by docetaxel treatment in LNCaP cells. [Oncogene] Abstract | |
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PUBLICATIONS(Ranked by impact factor of the journal)C4-2 cells were incubated with docetaxel, aneustat and docetaxel+aneustat to assess effects on cell migration. [Br J Cancer] Full Article WNT5A Induces Castration-Resistant Prostate Cancer via CCL2 and Tumor-Infiltrating Macrophages WNT5A was associated with increased expression of chemokine ligand 2 (CCL2) in the human metastatic prostate cancer cell line, LNCaP. Mechanistically, this induction of CCL2 by WNT5A was likely to be mediated via the mitogen-activated protein kinase/extracellular signal-regulated kinase signaling pathway. [Br J Cancer] Abstract Investigators explored the roles of ubiquitin-specific protease 10 (USP10) in prostate cancer progression in p53, G3BP2, and androgen receptor (AR) signaling. Using chromatin immunoprecipitation and sequence analysis, they found that USP10 is transcriptionally induced with AR recruitment to an intronic region. [Mol Cancer Res] Abstract Blockade of ACK1/TNK2 to Squelch the Survival of Prostate Cancer Stem-Like Cells To uncover tyrosine kinase/s critical for the survival of the CD44+PSA−/lo subpopulation, researchers performed an unbiased screen targeting 87 tyrosine kinases with gene specific siRNAs. Among a subset of tyrosine kinases crucial for prostate cancer stem-like cell survival, was a non-receptor tyrosine kinase, ACK1/TNK2, a critical regulator of castration resistant prostate cancer growth. [Sci Rep] Full Article The authors report that expression of mitochondrial ribosomal protein S18-2 (S18-2) was increased with disease progression in clinical specimens of prostate cancer (PCa). The level of induction of epithelial to mesenchymal cell transition correlated with the expression level of S18-2 in PCa cell lines. [Sci Rep] Full Article Osteoblast-derived factors increased migration of PC-3U cells, an effect less prominent in cells overexpressing a mutated type I TGFβ receptor preventing non-canonical TRAF6-dependent TGFβ signaling. [Prostate] Abstract P62 increased the levels of HDAC6 and reduced the acetylation of α-tubulin and the stability of microtubules. Consequently, high levels of P62 caused a promotion of epithelial-to-mesenchymal transition in addition to an impairment of autophagy flux, and further led to an enhancement of proliferation, migration, and invasion of prostate cancer cells. [Prostate] Abstract Scientists report a novel dendrimer conjugate modified to deliver the mammalian target of rapamycin (mTOR) inhibitor, rapamycin. In vitro analyses demonstrated that this drug conjugate, G5-FI-RGD-rapamycin, binds to prostate cancer cells and fibroblasts to inhibit mTOR signaling and VEGF expression. [J Cell Biochem] Abstract Researchers investigated thoroughly the effect of lncRNA PART1 on prostate cancer cells proliferation and apoptosis, through regulating toll-like receptor pathways. LncRNA PART1 expression was also examined by quantitative real-time polymerase chain reactions in human tissues and the cells lines LNCaP and PC3. [Biol Chem] Abstract | |
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REVIEWSEstrogen and Androgen Blockade for Advanced Prostate Cancer in the Era of Precision Medicine The authors summarize estrogen receptor (ER) and estrogen-related receptor signaling pathways, molecular diagnosis, and selective ER modulators as candidates for advanced prostate cancer treatment. [Cancers] Full Article Visit our reviews page to see a complete list of reviews in the prostate cell research field. | |
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INDUSTRY NEWSPanacea Pharmaceuticals announced the completion of patient enrollment in an open-label, parallel-designed, multi-center Phase I clinical trial of PAN-301-1 for the treatment of persistent prostate cancer to assess safety and immunogenicity. [Panacea Pharmaceuticals (PR Newswire Association LLC)] Press Release Syndax Announces Immuno-Oncology Clinical Trial Collaboration with AstraZeneca Syndax Pharmaceuticals, Inc. announced a new clinical collaboration with AstraZeneca to evaluate the safety and efficacy of AstraZeneca’s durvalumab, a human monoclonal antibody directed against programmed death-ligand 1, in combination with SNDX-6352, Syndax’s monoclonal antibody inhibitor of colony-stimulating factor 1 receptor, across a variety of solid tumors. [Syndax Pharmaceuticals, Inc.] Press Release | |
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POLICY NEWSBulgaria in the Cold as European Union Freezes Its Funding European Union science ministers are due to meet in their bloc’s poorest member state — Bulgaria — to discuss future EU research policy. For the host nation, it was supposed to be a chance to showcase its ambitious plans to boost economic growth by attracting international research institutes to the country. [Nature News] Editorial Kid Co-Authors in South Korea Spur Government Probe The South Korean government is expanding an investigation into researchers who named their children as co-authors on papers. The extended probe comes after a government report identified 82 academic papers on which authors had named their children or relatives — many of them in middle or high school — as co-authors on the publications. [Nature News] Editorial
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EVENTSNEW Advances in Cell and Tissue Culture (ACTC) 2018 Visit our events page to see a complete list of events in the community.
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JOB OPPORTUNITIESNEW Postdoctoral Fellow – Cancer Biology (Johns Hopkins University) NEW Scientist – Cancer Biology (Dana-Farber Cancer Institute) NEW Postdoctoral Fellow – Cancer Biology (University of Pennsylvania) Postdoctoral Fellow – Cancer Biology (Wake Forest Baptist Comprehensive Cancer Center) PhD Scholarships – Human Health & Emerging Environmental Contaminants (University of Hull) PhD Positions – Cancer Imaging (University of Hull) Postdoctoral Positions – Gene Regulation and/or Cancer Biology (University of North Carolina) Recruit Top Talent: Reach potential candidates by posting your organization’s career opportunities on the Connexon Creative Job Board at no cost.
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