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RAS

Oxysterol Binding Protein-Like 3 (OSBPL3) Is a Novel Driver Gene That Promotes Tumor Growth in Part through R-Ras/Akt Signaling in Gastric Cancer

[Scientific Reports] Gastric cancer (GC) is one of the most lethal malignant tumors. Researchers identified novel driver genes and clarified their roles in GC.

Involvement of C-Myc in Low Dose Radiation-Induced Senescence Enhanced Migration and Invasion of Unirradiated Cancer Cells

[Aging-Us] The authors found that conditioned medium harvested from WI-38 lung fibroblasts and H1299 lung adenocarcinoma cells exposed to 0.1Gy to 1Gy could enhance the migration and invasion of unirradiated H1299 cells in both 2D and 3D culturing circumstances.

Erasca Announces First Patient Dosed in HERKULES-3, a Phase Ib/II Gastrointestinal Cancer Master Protocol Evaluating ERAS-007 in Multiple Combinations

[Erasca, Inc.] Erasca, Inc. announced dosing of the first patient in HERKULES-3, a Phase Ib/II master protocol clinical trial evaluating ERAS-007 in combination with various agents in patients with gastrointestinal cancer, with initial focus on patients with advanced colorectal cancer.

RAS Induced Senescence of Skin Keratinocytes Is Mediated through Rho-Associated Protein Kinase (ROCK)

[Molecular Carcinogenesis] Researchers reported that the Rho-associated protein kinase (ROCK) signaling pathway was a critical regulator of oncogene-induced senescence in skin carcinogenesis.

Tetraspanin 6 Is a Regulator of Carcinogenesis in Colorectal Cancer

[Proceedings of the National Academy of Sciences of the United States of America] Using a combination of in vitro and in vivo assays, scientists demonstrate that Tspan6 functioned as a tumor suppressor in colorectal cancer by attenuating the epidermal growth factor receptor–based signaling axis.

Inhibiting BCKDK in Triple Negative Breast Cancer Suppresses Protein Translation, Impairs Mitochondrial Function, and Potentiates Doxorubicin Cytotoxicity

[Cell Death Discovery] TNBC cells treated with doxorubicin exhibited reduced branched-chain ketoacid dehydrogenase kinase (BCKDK) expression and intracellular branched-chain ketoacids (BCKAs). Genetic and pharmacological inhibition of BCKDK in TNBC cell lines also showed a similar reduction in intracellular and secreted BCKAs.

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