| Vol. 14.40 – 27 October, 2022 |
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| Investigators discovered that TNBCs had heterogeneous phenotypes in ferroptosis-related metabolites and metabolic pathways. [Cell Metabolism] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| Myosin-X (MYO10) promoted filopodia formation and cell invasion in vitro, and cancer-cell dissemination from progressively invasive human ductal carcinoma in situ xenografts. [Developmental Cell] |
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| Investigators showed that STAT5aca reduced the migratory and invasive ability of human breast cancer cell lines in vitro. They demonstrated that STAT5aca overexpression in human breast cancer cells lowered their metastatic burden in xenografted mice. [Oncogene] |
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| Tissue factor blockade caused a reduction in epithelial-to-mesenchymal-transition, cancer stemness, and expression of the pro-metastatic markers Slug and SOX9 in several breast cancer cell lines and in ex vivo cultured tumor cells. [Oncogene] |
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| Scaffolds displayed high in vitro stability with 90% of mass remaining after 14 days of culture. They were also highly biocompatible, and capable of supporting the attachment, infiltration and proliferation of MCF7 breast cancer cells. [Biomaterials Advances] |
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| RBCK1 over-expression inhibited TNBC cell progression in vitro and in vivo, while RBCK1 depletion promoted TNBC cell invasion. [Cell Communication and Signaling] |
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| Scientists found that the long noncoding RNA HOTAIR is highly expressed in breast cancer stem cells (CSCs). HOTAIR was required for breast CSC self-renewal and tumor propagation. [Journal of Biological Chemistry] |
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| The authors summarize the evolution of (neo)adjuvant trials from the pre-genomic to the post-genomic era and provide critical insights into how neoadjuvant studies are currently designed, discussing the need for better end points. [Nature Reviews Clinical Oncology] |
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| Scientists present the state of the art of 3D bioprinted cancer modelling, focusing on the biological processes that underlie the molecular mechanisms involved in cancer progression and treatment response as well as on proteomic and genomic signatures. [Nature Reviews Cancer] |
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| BriaCell Therapeutics Corp. announced the completion of the Phase I part of the clinical trial of its lead candidate, Bria-IMT™, in combination with Incyte’s PD-1 inhibitor, retifanlimab, in advanced breast cancer. [BriaCell Therapeutics Corp.] |
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| January 29 – February 2, 2023 Banff, Alberta, Canada |
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| AstraZeneca – Mississauga, Ontario, Canada |
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| Ludwig Maximilians University of Munich – Munich, Germany |
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| Nature Communications – London, Berlin, New York, Shanghai (Hybrid) |
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| NCI – Bethesda, Maryland, United States |
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| Italian Institute of Technology – Genoa, Italy |
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