ADV-CRISPR-SaCas9-mediated MECOM depletion inhibits tumor growth in LUSC PDX models
(A and B) Three types of viruses (ADV, 1 × 1010 VP; lentivirus, 1 × 109 VP; AAV2, 1 × 1012 VP) expressing GFP were intratumorally injected into the LUSC021 PDX model (NOD-SCID mice). The representative images (A) and infection efficiencies (B) of ADV, lentivirus, and AAV2 in the tumors isolated from those mice treated with different viruses by flow cytometry detection.
(C–F) A diagram (C) for intratumoral administration of ADV-CRISPR-SaCas9-mediated MECOM depletion in PDX models (NOD-SCID mice). The ADV system was intratumorally injected at days 0 and 12 with the amounts of 1.0 × 1010 VP and 0.5 × 1010 VP, respectively. Tumor growth curves and representative tumor photos of PDX models including LUSC006 (D), LUSC018 (E), and LUSC021 (F) treated with MECOM-depleted ADV (MECOM-KO) or control ADV. Scale bars, 1 cm. n = 5. ∗p < 0.05, unpaired 2-tailed t test.