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Image Search Results
Journal: Cell reports. Medicine
Article Title: KRAS G12D -driven pentose phosphate pathway remodeling imparts a targetable vulnerability synergizing with MRTX1133 for durable remissions in PDAC.
doi: 10.1016/j.xcrm.2025.101966
Figure Lengend Snippet: Figure 2. G6PD inhibition reduces malignancy and resistance to MRTX1133 in KRASG12D-mutated PDAC (A) Heatmap illustrating organoid area fold changes and synergy indexes with MRTX1133 following treatment with the indicated inhibitors. Measurements taken 6 days post treatment. Organoid area fold changes and synergy indexes are represented by the indicated values of different colors and sizes. (B) Synergy analysis of RRx-001 and MRTX1133 using the Loewe model in KPC organoids. (C–E) Representative images of pancreatic tissues from KC mice stained with H&E, Alcian blue, and amylase/CK19 with or without RRx-001 treatment (5 mg/kg/ day) (C). Quantification of the total (D) and differential-grade (E) area of precancerous lesions in the entire pancreatic tissue section (n = 6). (F) Representative images and quantification of pan-keratin and Ki67 staining in PDAC tissues from KPC allografts and PDX-1 models, with and without RRx-001 treatment (5 mg/kg/day) (n = 6). (G and H) Tumor growth of KPC allografts (G) and PDX-1 (H) models with or without RRx-001 (n = 6). (I–L) Tumor growth and survival analysis of KPC allografts (I and J) and PDX-1 (K and L) models treated with RRx-001 (5 mg/kg/day) and/or MRTX1133 (30 mg/kg/ day) (n = 6).
Article Snippet: For drug intervention studies,
Techniques: Inhibition, Staining