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breast cancer

MiR-9-3p Regulates the Biological Functions and Drug Resistance of Gemcitabine-Treated Breast Cancer Cells and Affects Tumor Growth through Targeting MTDH

[Cell Death & Disease] Scientists explored the role of MTDH in regulating the sensitivity of breast cancer cell lines to gemcitabine and the potential miRNAs targeting MTDH.

SNAI1-Mediated Transcriptional Regulation of Epithelial-to-Mesenchymal Transition Genes in Breast Cancer Stem Cells

[Cellular Signalling] Researchers performed in silico analysis of microarray data from luminal, Her2+, and triple-negative breast cancer cell lines and identified 15 relatively unexplored epithelial-to-mesenchymal (EMT)-related differentially expressed genes along with the markedly high expression of EMT-transcription factor, SNAI1.

The Immunotherapy Candidate TNFSF4 May Help the Induction of a Promising Immunological Response in Breast Carcinomas

[Scientific Reports] Investigators identified the oncogenic features of TNFSF4 in breast carcinoma. TNFSF4 was revealed to be closely related to treatment that induced antitumor immunity and to interact with multiple immune effector molecules and T cell signatures

Compromised Nuclear Envelope Integrity Drives TREX1-Dependent DNA Damage and Tumor Cell Invasion

[Cell] Scientists showed that nuclear envelope ruptures induced DNA damage that promoted senescence in non-transformed cells and induced an invasive phenotype in human breast cancer cells.

Three-Dimensional Covalent Organic Frameworks with Cross-Linked Pores for Efficient Cancer Immunotherapy

[Nano Letters] Mechanism studies revealed that after linking these immunogenic cell death inert monomers into the covalent organic frameworks (COFs) backbone, the optical properties of these COFs could be systematically tuned to achieve excellent reactive oxygen species production performance.

RASSF1C Oncogene Elicits Amoeboid Invasion, Cancer Stemness, and Extracellular Vesicle Release via a SRC/Rho Axis

[EMBO Journal] Investigators showed that the novel oncogene RASSF1C drove mesenchymal-to-amoeboid transition and stem cell attributes in breast cancer cells. Mechanistically, RASSF1C activated Rho/ROCK via SRC-mediated RhoGDI inhibition, resulting in generation of actomyosin contractility.

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