| Vol. 15.43 – 2 November, 2023 |
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| Scientists showed that standard-of-care therapy caused DNA damage and toxic PARP1 trapping upon generation of a functional BRCAness phenotype, leading to increased histone parylation and reduced H3K9 acetylation, resulting in transcriptional blockage and cell death. [Nature Communications] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| Researchers utilized an in silico-designed glucocorticoid receptor (GR) activity signature to demonstrate that GR related to the proliferative capacity of numerous primary cancer types. [EMBO Molecular Medicine] |
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| The authors found metabolic reprogramming that increased fatty acid β-oxidation in estrogen receptor-alpha positive breast cancers as a mechanism of resistance to endocrine therapy. [Cancer Research] |
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| Researchers revealed an additional dimension of regulator of chromosome condensation domain-containing protein 1 (RCCD1) functionality in regulating mitochondrial homeostasis, whose dysregulation inflicted pathologic states such as breast cancer. [Oncogene] |
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| The authors characterized the migratory phenotype of MDA-MB-231 cells, using functionalized IGDQ-exposing surfaces, and compared it to integrin A5 and integrin B3 knock-down cells. [Cell Communication and Signaling] |
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| Scientists explored the role of NLRX1 in the highly metastatic murine 4T1 mammary tumor model. They demonstrated that NLRX1 functions as a tumor suppressor when expressed in the host cells. [Journal of Immunology] |
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| Knockdown of zinc finger protein 148 (ZNF-148) suppressed malignant phenotypes, including cell proliferation, epithelial-mesenchymal transition, and tumorigenesis in vitro and in vivo, while ZNF-148 overexpression had the opposite effects. [Cancer Medicine] |
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| The molecular effects of long-term ceramide synthase 4 (CerS4) overexpression on breast cancer progression and migration were explored using TCGA-BRCA data, MCF-7 cells stably overexpressing CerS4, and doxorubicin-resistant MCF-7 cells. [Lipids in Health and Disease] |
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| Investigators demonstrated that Ezetimibe inhibited the PDGFR/AKT pathway, thereby halting TNBC cycle progression and tumor growth. [Heliyon] |
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| The reactivation of estrogen receptor alpha (ER-α), presents a potential strategy to re-sensitize TNBC to hormonal therapy. Scientists provide up-to-date information related to the direct involvement of miRNA in regulating the translation of ER-α mRNA. [Molecular Cancer Research] |
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| The group behind the radical open-access initiative Plan S has announced its next big plan to shake up research publishing — and this one could be bolder than the first. It wants all versions of an article and its associated peer-review reports to be published openly from the outset, without authors paying any fees. [Nature News] |
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| December 4 – 7, 2023 Dublin, Ireland |
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| Baylor College of Medicine – Houston, Texas, United States |
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| University of Pennsylvania – Philadelphia, Pennsylvania, United States |
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| Baylor College of Medicine – Houston, Texas, United States |
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| University of Galway – Galway, Ireland |
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| Cedars-Sinai – Los Angeles, California, United States |
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