Keep Current with the Latest in Cell Biology Research

ENHERTU® Plus Pertuzumab Type II Variation Application Validated in the EU as First-Line Treatment of Patients with HER2 Positive Metastatic Breast Cancer

[Daiichi Sankyo] The European Medicines Agency has validated the Type II Variation marketing authorization application for ENHERTU® (trastuzumab deruxtecan) in combination with pertuzumab for the first-line treatment of adult patients with unresectable or metastatic HER2 positive breast cancer.

The UFL1-AKT Positive Feedback Loop Promotes Breast Cancer Progression by Enhancing Lipid Synthesis

[Nature Communications] Investigators revealed a critical role for UFMylation in lipid metabolism and identify the UFL1-AKT axis as a potential therapeutic target in breast cancer.

Crotonate Suppresses Breast Cancer Metastasis and Promotes Immunotherapy Response by Inducing ACSS2-Mediated EZH2-K348 Crotonylation

[Science Advances] Scientists presented a crotonate–crotonyl–coenzyme A–enhancer of zeste homolog 2 (EZH2) crotonylation cascade blocking breast cancer growth and metastasis.

Chemotherapy-Treated Breast Cancer Cells Activate the WNT Signaling Pathway to Enter a Diapause-Like Early Persister State

[Cancer Research] Investigators showed that following chemotherapy, diverse therapeutic agents converge on WNT pathway activation to induce a de novo diapause-like cell state across various TNBC line, xenograft, and patient-derived organoid models.

Positive Feedback Regulation between USP8 and Hippo/YAP Axis Drives Triple-Negative Breast Cancer Progression

[Cell Death & Disease] Researchers revealed a forward feedback loop between Ubiquitin Specific Peptidase 8 (USP8) and Hippo signaling in TNBC, indicating USP8 as a potential therapeutic drug targets in TNBC.

Reversing the Hypoxic Adaptive Response in Breast Cancer Cells through Small-Molecule Inhibition of Oncogenic MicroRNA-21

[Journal of Medicinal Chemistry] The authors identified new pre-microRNA-210 (miR-210) ligands, which exhibited a submicromolar affinity for the miR-210 precursor and potently inhibited its maturation in vitro.

Transformation of Nanoparticles Into Hydrogels for Long-Acting and Sensitized Apoptosis Therapy of Triple Negative Breast Cancer

[Biomaterials Science] Researchers developed a pH-responsive nanoparticle-to-hydrogel system for long-lasting retention of tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) receptors at the tumour site and promoting apoptosis in TRAIL-sensitive TNBC cells.

Dinuclear Cu2+-Complexes Disrupt Cellular Pathways and Rewire the Breast Cancer Proteome

[Journal of Proteomics] Scientists investigated the antitumor potential of two novel dinuclear Cu2-complexes, [Cu2(μ-CH3COO)(L)(OH2)]·2H2O and [Cu2(μ-OH)(HL)(OH2)]ClO4·2H2O, in MCF-7 breast cancer cells.

ZNF384-Regulated SLC31A1 Expression Promotes Tumor Proliferation and Invasion in Breast Cancer

[Molecular and Cellular Biochemistry] The authors explored the function and potential regulatory mechanisms of SLC31A1 in breast cancer. SLC31A1 expression was significantly elevated in breast cancer tissues, and high expression was associated with poor prognosis.

Modulated Calcium-Sensing Receptor (CaSR) Expression in Human Breast Cancer Provided Insights Into Tumor Progression and Therapeutic Potential

[Journal of the Egyptian National Cancer Institute] Scientists investigated CaSR gene expression levels, its correlation with oncogenic pathways, and its protein localization in human breast cancer tissues.

Opioids in Breast Cancer: Between Analgesia and Modulation of Tumor Progression

[British Journal of Pharmacology] Investigators synthesize the available evidence on the role of the opioid system in breast cancer, with particular emphasis on molecular mechanisms of receptor signalling, their interactions within the tumour microenvironment, and the clinical implications for pain management.

Reactive Oligodendrocytes Promote Glioblastoma Progression through CCL5/CCR5-Mediated Glioma Stem Cell Maintenance

[Neuron] Researchers utilized single-cell and spatial transcriptomics from primary and recurrent glioblastoma (GBM) tumors, immunohistochemistry, cytokine profiling, and migration assays to show that GBM cells recruit oligodendrocytes to the tumor border via fractalkine signaling.

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