Journal: Journal of Cancer

Article Title: UC2288 induces cell apoptosis of nasopharyngeal carcinoma cells via inhibiting EGFR/ERK pathway

doi: 10.7150/jca.48282

Figure Lengend Snippet: UC2288 inhibited EGFR/ERK pathway. ( A-B ) The expression of p-EGFR/EGFR and p-ERK1/2/ERK was examined by western blot. Data are expressed as mean ± SD, n=3. ** p < 0.01 and *** p < 0.001 compared to control. ( C-D ) Pretreatment with epidermal growth factor (EGF), CCK-8 assay was conducted to evaluate the cell viability. Data are expressed as mean ± SD, n=3. ## p < 0.01 compared to the UC2288 (4 µM)-treated group.

Article Snippet: UC2288 (purity ~99%) and human recombinant epidermal growth factor (EGF) were purchased from Abcam (Cambridge, UK), and dissolved in dimethyl sulfoxide (DMSO) and water, respectively.

Techniques: Expressing, Western Blot, CCK-8 Assay

Journal: NPJ Regenerative Medicine

Article Title: Scaffolds with spatiotemporally controlled growth factor delivery and cyclodextrin-enabled antagonism of growth factor receptor sequestration promote cutaneous wound healing

doi: 10.1038/s41536-025-00431-0

Figure Lengend Snippet: a Images of splinted db/db mouse wounds at day 10 post wounding. b Quantification of migrating epithelial tongues from splinted db/db mouse wounds [Error bars correspond to standard deviations from 4 biological specimens with statistical significance assessed using paired 2-way ANOVA followed by Tukey’s multiple comparison testing, * p < 0.05, ** p < 0.01, **** p < 0.0001]. c IHC staining and d quantification of CD31 + cells/mm 2 demonstrating increased number blood vessels with HβCD + EGF treatment [Error bars correspond to standard deviations from four biological specimens with statistical significance assessed using paired student t -test, **** p < 0.0001] (E-epidermis, D-dermis; scale bar = 50 µm). d ELISA demonstrating increased levels of VEGF in splinted db/db mouse wounds upon incorporation of growth factors into HβCD hydrogels [Error bars correspond to standard deviations from four biological specimens with statistical significance assessed using paired 2-way ANOVA followed by Tukey’s multiple comparison testing, * p < 0.05, ** p < 0.01, **** p < 0.0001]. (scale bar = 50 µm).

Article Snippet: For determination of growth factor release from the hydrogels, gelatin hydrogels were loaded onto 0.4 μm PET membranes within a 24 well plate, submerged in PBS, and growth factor release quantified at 0, 12, 24, 48, 96 and 120 h using respective Quantikine ELISA kits (R&D Systems, DEG00 for EGF, DBB00 for PDGF-BB, and DVE00 for VEGF).

Techniques: Comparison, Immunohistochemistry, Enzyme-linked Immunosorbent Assay