Abstract
Background: The precise roles for Rictor/Sin1 complexes in IFN signaling remain to be defined. Results: Targeted disruption Rictor/Sin1 results in defects in activation of elements of Stat pathways. These proteins are required for IFN antineoplastic effects on malignant erythroid precursors. Conclusion: Rictor/Sin1 play critical roles in IFN signaling. Significance: This study provides evidence for a key mechanism for gene regulation associated with generation of IFN antineoplastic responses.
Original language | English (US) |
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Pages (from-to) | 6581-6591 |
Number of pages | 11 |
Journal | Journal of Biological Chemistry |
Volume | 289 |
Issue number | 10 |
DOIs | |
State | Published - Mar 7 2014 |
ASJC Scopus subject areas
- Molecular Biology
- Biochemistry
- Cell Biology