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Complementation of Human Papillomavirus Type 16 E6 and E7 by Jagged1-Specific Notch1-Phosphatidylinositol 3-Kinase Signaling Involves Pleiotropic Oncogenic Functions Independent of CBF1;Su(H);Lag-1 Activation
J. Virol. Veeraraghavalu et al. 79: 7889

Supplemental material

Files in this Data Supplement:

  • Supplemental file 1 - Fig. S1. Expression levels of endogenous Notch1 and Notch2 in HaCaT cells and stable expression levels of Jagged1 and HA-tagged Delta1 in HaCaT-Jagged1 and HaCaT Delta cell lines, respectively. Also shown are levels of phospho-PKB/AKT (ser-473) in subcutaneous tumors generated by HaCaT cells expressing a combination of genes.
    Fig. S2. Jagged1 expression leads to induction PI3K-mediated generation of anoikis resistance.
    Fig. S3. Expression level of plakoglobin in HaCaT cells stably expressing mock vector (HaCaT-Neo) or Jagged1 (HaCaT-Jag1) at 20 h postwounding. The changes in expression of EMT markers in SiHa cells at 40 h in an in vitro wound healing assay are shown.
    Fig. S4. Jagged1-induced PI3K activation and anoikis resistance is independent of CSL-mediated Notch signaling.
    Fig. S5. Tumor volume in nude mice after 3 weeks of subcutaneous infection of HaCaT cells stably expressing mock vector (Neo) or C-terminal PDZ-binding motif mutant Jagged1. PDF document, 200K.
  • Supplemental file 2 - : Table. S1. C-terminal PDZ-ligand motif mutant Jagged1 cooperates with HPV-16 E6 and E7 in transformation of HaCaT cells in in vitro soft agar colony formation assays.
    Table S2. List of genes either up- or downregulated in the microarray analysis of HaCaT cells stably expressing either Jagged1 or Delta1.

    PDF document, 325K.





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