| Vol. 13.12 – 1 April, 2021 |
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| A single-cell breast cancer mass cytometry panel was optimized to identify cell phenotypes and their oncogenic signaling states in a biobank of patient-derived tumour xenograft models representing the diversity of human breast cancer. [Nature Communications] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| Researchers uncovered that Adipogenesis associated Mth938 domain containing (AAMDC) regulated the expression of several metabolic enzymes involved in the one-carbon folate and methionine cycles, and lipid metabolism. [Nature Communications] |
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| Scientists investigated the role of MCL-1 in clinically relevant breast cancer models and addressed whether the canonical role of MCL-1 in apoptosis, which could be targeted using BH3-mimetic drugs, was the major function for MCL-1 in breast cancer. [Cell Death & Differentiation] |
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| The authors showed that LXR ligands confered chemotherapy resistance in TNBC cell lines and xenografts, and that LXRalpha was necessary and sufficient to mediate this resistance. [Oncogene] |
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| By exploring the regulatory mechanisms of estrogen receptor α (ERα) at levels of post-translational modifications, investigators identified the deubiquitinase USP15 as a novel protector for preventing ERα degradation and a critical driver for breast cancer progression. [Cell Death & Disease] |
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| Researchers utilized an established Met-dependent transgenic mouse model of TNBC, human cell lines and patient-derived xenografts to investigate the role of MET in TNBC tumorigenesis. [npj Breast Cancer] |
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| An analogous truncated mouse prolactin receptor (mPRLr) was found to be oncogenic when co-expressed with wild-type mPRLr. The authors determined if a similar transforming event occurs with the hPRLr in human breast epithelial cells. [npj Breast Cancer] |
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| Researchers showed that β3 integrin induction by the bone microenvironment promotes resistance to chemotherapy through an altered metabolic response that can be defused by combination with αvβ3-targeted mTORC1 inhibitor nanotherapy. [Molecular Cancer Therapeutics] |
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| Scientists showed that RANK bound to HER2 in breast cancer cells and that enhanced RANK pathway activation altered HER2 phosphorylation status. [Breast Cancer Research] |
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| The authors investigated the antitumor potential of the most potent compounds in citrus peels on breast cancer by exploring their anti-estrogenic and anti-aromatase activities. [Scientific Reports] |
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| Researchers systematically compared the transcriptomes of these different culture conditions by RNAseq of 14 breast cancer cell lines cultured in both 2D and 3D conditions. [Scientific Reports] |
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| Investigators demonstrated that the miRNA miR-142-3p directly targeted the 3′ untranslated region of HMGA2, which encoded an onco-embryonic protein that was overexpressed in most cancers, including breast cancer. [Life Sciences] |
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| The authors emphasized on the prospective future applications of 3D bioprinted cancer models for rapid and accurate drug screening in breast cancer. [Journal of Controlled Release] |
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| Merck announced that the FDA has issued a Complete Response Letter regarding Merck’s supplemental Biologics License Application seeking approval for KEYTRUDA, the company’s anti-PD-1 therapy, for the treatment of patients with high-risk early-stage triple-negative breast cancer, in combination with chemotherapy as neoadjuvant treatment, then continuing as a single agent as adjuvant treatment after surgery. [Merck (BusinessWire, Inc.)] |
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| June 28 – 30, 2021 Virtual |
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| The University of Texas Southwestern Medical Center – Dallas, Texas, United States |
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| Thomas Jefferson University – Philadelphia, Pennsylvania, United States |
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| University of Arizona Cancer Center – Tucson, Arizona, United States |
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| Baylor College of Medicine – Houston, Texas, United States |
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