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Additional file 3 of Identifying and exploiting combinatorial synthetic lethality by characterizing adaptive kinome rewiring of EGFRvIII-driven glioblastoma

Title: Additional file 3 of Identifying and exploiting combinatorial synthetic lethality by characterizing adaptive kinome rewiring of EGFRvIII-driven glioblastoma
Authors: Benjamin Lin; Abigail K. Shelton; Erin Smithberger; Julia Ziebro; Kasey R. Skinner; Ryan E. Bash; Richard Kirkman; Allie Stamper; Madison Butler; Alex Flores; Steven P. Angus; Michael P. East; Timothy F. Cloughesy; David A. Nathanson; Michael E. Berens; Jann N. Sarkaria; Zev A. Binder; Donald M. O’Rourke; Timothy C. Howton; Brittany N. Lasseigne; Christopher D. Willey; Gary L. Johnson; Anita B. Hjelmeland; Frank B. Furnari; C. Ryan Miller
Publication Year: 2025
Collection: The University of Auckland: Figshare
Subject Terms: Biochemistry; Medicine; Genetics; Pharmacology; Biotechnology; Marine Biology; Cancer; Hematology; Virology; Computational Biology; Biological Sciences not elsewhere classified; Chemical Sciences not elsewhere classified; EGFR; Glioblastoma; Synthetic lethality; Kin­ome rewiring; Upfront combinatorial therapy
Description: Supplementary Material 3: Fig. S2 EGFRvIII (hEGFR) overexpression reprograms the receptor kinase transcriptome. Unsupervised hierarchical clustering heatmaps (AB) and volcano plots (CD) of DE receptor kinases at the mRNA level in both full (A) and starved (B) culture conditions show consistent downregulation in CEv3 (C) and C (D) cells. Full and starved serum cultures are denoted FS and SS, respectively
Document Type: still image
Language: unknown
DOI: 10.6084/m9.figshare.29431972.v1
Availability: https://doi.org/10.6084/m9.figshare.29431972.v1; https://figshare.com/articles/figure/Additional_file_3_of_Identifying_and_exploiting_combinatorial_synthetic_lethality_by_characterizing_adaptive_kinome_rewiring_of_EGFRvIII-driven_glioblastoma/29431972
Rights: CC BY
Accession Number: edsbas.6A00A12E
Database: BASE