| Vol. 13.22 – 10 June, 2021 |
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| Investigators illustrated how BARD1 simultaneously recognized the DNA damage-induced mark H2AK15ub and DNA replication-associated mark H4K20me0 on the nucleosome. [Molecular Cell] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| The authors showed that genetic deletion of the Endo180 (MRC2) receptor, predominantly expressed by a population of matrix-remodeling cancer-associated fibroblasts, profoundly limited tumor growth and metastasis; effects that could be recapitulated in 3D co-culture assays. [Nature Communications] |
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| Scientists created homogeneous antibody-drug conjugates containing two distinct payloads that showed HER2-specific cell killing potency, desirable pharmacokinetic profiles, minimal inflammatory response, and marginal toxicity at therapeutic doses. [Nature Communications] |
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| Researchers explored whether the microbiome of the gut and mammary gland mediates the dietary effects on breast cancer. In vitro models of the normal breast epithelium showed that lipopolysaccharide disrupted tight junctions and compromised epithelial permeability. [Cancer Research] |
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| Investigators showed that a unique anti-human CD81 antibody (5A6) effectively halted invasion of TNBC cell lines. They demonstrated that 5A6 induced CD81 clustering at the cell membrane and implicated JAM-A protein in the ability of this antibody to inhibit tumor cell invasion and migration. [Proceedings of the National Academy of Sciences of the United States of America] |
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| Researchers showed that cytoplasmic complexes composed of steroid receptor co-activators, PELP1 and SRC-3, modulated breast cancer stem cell expansion through upregulation of the HIF-activated metabolic target genes PFKFB3 and PFKFB4. [Oncogene] |
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| DDR1 knockdown and DDR1 pharmacological inhibitor decreased cell growth and inhibited cell cycle progression in breast cancer cell lines, while enhanced the sensitivity of PIK3CA/AKT1 mutant cells to palbociclib. [Oncogene] |
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| Scientists used a library of peptides from diverse prokaryal genomes to screen macromolecular interactions promoting the nuclear relocalization of Forkhead Box O3 (FOXO3a) and assessed the impact of transcriptional changes on the growth of breast cancer cell lines. [Cell Chemical Biology] |
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| The authors investigated the metabolic vulnerabilities of TNBC, particularly those metabolic perturbations that increased mitochondrial apoptotic priming and sensitivity to BH3 mimetics. [Science Signaling] |
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| Oxytocin receptor overexpression led to an activation of prolactin/p-STAT5 pathway and created a microenvironment that promoted mammary-specific tumorigenesis. [Cell Death & Disease] |
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| Compared to normal mammary gland tissues, cross-linked hyaluronan levels were significantly decreased in breast cancer and associated with tumor malignancy. [Cell Death & Disease] |
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| Using an in vitro model of epithelial to mesenchymal transition (EMT), investigators showed that nitrofen interfered with the process of EMT and promoted mesenchymal to epithelial transformation. [Scientific Reports] |
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| Among 759 specimens, immunohistochemistry exhibited glycoprotein non-metastatic B (GPNMB) expressions were variable in different subtypes and significantly higher in TNBC. GPNMB positively correlated with epithelial–mesenchymal transition regulators, mesenchymal marker vimentin, MMP and integrins. [Scientific Reports] |
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| The authors highlight the association of several long noncoding RNAs in TNBC progression and treatment, along with their possible functions and mechanisms. [Journal of Cellular Physiology] |
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| Investigators discuss 3D cell culture systems as mammosphere organoids and their relevance for agronomic research. [Veterinary Research] |
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| Byondis B.V. announced positive results from the Phase III TULIP® study. The trial compared the efficacy and safety of the company’s antibody-drug conjugate trastuzumab duocarmazine to physician’s choice treatment in patients with pretreated HER2-positive unresectable locally advanced or metastatic breast cancer. [Byondis B.V.] |
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| Gilead Sciences, Inc. – Foster City, California, United States |
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| Cedars-Sinai Medical Center – Los Angeles, California, United States |
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| Icahn School of Medicine at Mount Sinai – New York City, New York, United States |
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| University of Texas Southwestern Medical Center – Dallas, Texas, United States |
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| The University of Texas MD Anderson Cancer Center – Houston, Texas, United States |
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