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melanoma

Downregulation of Sperm-Associated Antigen 5 Inhibits Melanoma Progression by Regulating Forkhead Box Protein M1/a Disintegrin and Metalloproteinase 17/NOTCH1 Signaling

[Bioengineered] Downregulation of sperm-associated antigen 5 repressed malignant melanoma cell growth and epithelial to mesenchymal transition, which might be induced by inactivation of the forkhead box protein M1/A disintegrin and metalloproteinase 17/NOTCH1 signaling.

Circulating Tumor DNA in Melanoma—Clinic Ready?

[Current Oncology Reports] The authors examine the potential role of circulating tumor DNA as a clinical tool to inform clinical decision-making from early to late stage cutaneous melanoma.

Immune Checkpoint Inhibitors for the Treatment of Melanoma

[Expert Opinion On Biological Therapy] The authors describe the mechanisms of immune checkpoint activation and inhibition, second, andsummarize the results obtained with immune checkpoint inhibitorin melanoma treatment in terms of efficacy.

Non-Invasive Detection and Complementary Diagnostic of Liver Metastases via Chemokine Receptor 4 Imaging

[Cancer Gene Therapy] Scientists observed the elevated expression of chemokine receptor 4 (CXCR4) in uveal melanoma (UM) patient liver tissues, and high CXCR4 expression in liver metastases of UM murine models, regardless of the expression levels in the primary tumors.

NeoImmuneTech Announces First Patient Dosed in Phase II Study of NT-I7 (efineptakin alfa) with PD-L1 Checkpoint Inhibitor in High-Risk Skin Cancers

[NeoImmuneTech, Inc. (Businesswire, Inc.)] NeoImmuneTech, Inc. announced that the first patient has been dosed in the Phase IIa portion of a study evaluating NT-I7, a novel long-acting human interleukin-7, in combination with the PD-L1 targeting drug atezolizumab, in patients with advanced high-risk skin cancers including melanoma, merkel cell carcinoma, and cutaneous squamous cell carcinoma.

Loss of Glucose 6-Phosphate Dehydrogenase Function Increases Oxidative Stress and Glutaminolysis in Metastasizing Melanoma Cells

[Proceedings of the National Academy of Sciences of the United States of America] Glucose 6-phosphate dehydrogenase (G6PD) mutant melanomas had significantly decreased G6PD enzymatic activity and depletion of intermediates in the oxidative pentose phosphate pathway.

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