| Vol. 15.48 – 7 December, 2023 |
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| Scientists derived a dormancy-associated residual tumor cell signature that mirrored the transcriptional response to neoadjuvant therapy in patients and was enriched for extracellular matrix-related pathways. [Cancer Cell] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| Investigators developed a stem cell factor SOX9-based reporter for isolating CSCs in primary tumors and metastases of spontaneous mammary tumor models. [Science Advances] |
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| The authors observed that osteoclasts reduced the sensitivity of breast cancer cells to DNA damaging agents, including cisplatin and the PARP inhibitor olaparib. [Cancer Research] |
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| Researchers showed that in contrast to other subtypes, inositol monophosphatase 2 (IMPA2) was dramatically increased in basal-like breast cancer. [Cancer Letters] |
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| Scientists investigated the evolution and mechanistic heterogeneity in clonal populations of cell models for estrogen receptor (ER) positive breast cancer. [npj Breast Cancer] |
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| The authors investigated the beneficial role and mechanism of miRNA-34a-based gene therapy as a novel approach for conquering drug resistance mediated by ATP-binding cassette (ABC) transporters in breast cancer cells. [Breast Cancer Research and Treatment] |
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| Researchers uncovered the tumorigenic and prognostic role of dolichyl-phosphate mannosyltransferase subunit 2 (DPM2) in breast cancer, cellular assays, and bioinformatics analysis highlighted DPM2 as oncogene via inhibited cancer-related signaling pathways in breast cancer. [Environmental Toxicology] |
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| The authors investigated the regulatory mechanisms and roles of SRY-box transcription factor 10 (SOX10) in basal-like breast cancer progression. [Heliyon] |
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| Investigators showed that BUBR1 loss inhibited the phosphorylation of TAK1/JNK. In vitro and in vivo studies indicated the knockdown of BUBR1 rendered the breast cancer cells more sensitive to cisplatin. [In Vitro Cellular & Developmental Biology – Animal] |
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| Scientists review the current state of published knowledge with regard to breast cancer to identify relevant key mechanisms for inclusion into breast cancer adverse outcome pathways and to concurrently map non-animal methods addressing these key events. [Discover Oncology] |
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| MEDSIR presented the design of the MiRaDor trial conducted in collaboration with OncoclÃnicas & Co, which aims to evaluate the usefulness of ctDNA analysis to detect minimal residual disease in patients who had hormone receptor-positive/HER2-negative early breast cancer and are at high-risk of relapse. [MEDSIR (PRNewswire)] |
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| February 14 – 18, 2024 Cancun, Mexico |
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| International Iberian Nanotechnology Laboratory – Braga, Portugal |
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| University of Melbourne – Melbourne, Australia |
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| Zhejiang Chinese Medical University – Hangzhou, China |
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| BC Cancer – Vancouver, British Columbia, Canada |
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| Swammerdam Institute for Life Sciences – Amsterdam, Netherlands |
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