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Supplementary Figure S3 from Structural Basis for Multivalent MUC16 Recognition and Robust Anti-Pancreatic Cancer Activity of Humanized Antibody AR9.6

Year: 2024
Type: supplementary-materials
Abstract: Fig. S3. MUC16 expression in PDAC cells and PDAC patients’ samples using huAR9.6 mAb. (A) Western blotting for MUC16 (with huAR9.6) in normal HPDE cells and AsPC-1, T3M4, Capan-2, Panc-1, MiaPaCa-2, Capan-1, BxPC-3, S2-013, FG and SU86.86 PDAC cells. Loading control: α-tubulin. (B) Immunofluorescent staining for MUC16 (AF647-huAR9.6, red) and α-tubulin (AF488, green) in T3M4-WT and T3M4-MUC16KO cells. (C) Representative image of immunofluorescent staining for MUC16 (AF647-huAR9.6, red) in normal pancreas (n=7) and PDAC tissue (n=32) obtained from the Rapid Autopsy Program at UNMC. (D) Representative images of immunohistochemistry for MUC16 on a patient-derived xenograft (PDX) microarray using huAR9.6; (E) Graphical representation of varying histoscores; (F) Graphical representation of consistency between histoscore (huAR9.6-based MUC16 detection) and RNA sequencing of MUC16 gene expression in PDX microarray samples (n = 31). (G) Western blotting for MUC16 (with huAR9.6) in ascites fluids (n = 34) obtained from PDAC patients via the Rapid Autopsy Program at UNMC. Western blot of N-glycanase, O-glycanase and sialidase treated (H) T3M4 cell lysates and (I) MUC16 TR1.2 glycopeptides probed with huAR9.6 mAb. Detection of α-tubulin served as the loading control.
Language: English
Subfield: Oncology
Field: Medicine
Open Access status: gold
OpenAlex ID: W4399342973
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