TY - JOUR
T1 - Interferon receptor signaling in malignancy
T2 - A network of cellular pathways defining biological outcomes
AU - Fish, Eleanor N.
AU - Platanias, Leonidas C.
N1 - Publisher Copyright:
©2014 American Association for Cancer Research.
PY - 2014/12/1
Y1 - 2014/12/1
N2 - IFNs are cytokines with important antiproliferative activity and exhibit key roles in immune surveillance against malignancies. Early work initiated over three decades ago led to the discovery of IFN receptor activated Jak-Stat pathways and provided important insights into mechanisms for transcriptional activation of IFN-stimulated genes (ISG) that mediate IFN biologic responses. Since then, additional evidence has established critical roles for other receptor-activated signaling pathways in the induction of IFN activities. These include MAPK pathways, mTOR cascades, and PKC pathways. In addition, specific miRNAs appear to play a significant role in the regulation of IFN signaling responses. This review focuses on the emerging evidence for a model in which IFNs share signaling elements and pathways with growth factors and tumorigenic signals but engage them in a distinctive manner to mediate antiproliferative and antiviral responses.
AB - IFNs are cytokines with important antiproliferative activity and exhibit key roles in immune surveillance against malignancies. Early work initiated over three decades ago led to the discovery of IFN receptor activated Jak-Stat pathways and provided important insights into mechanisms for transcriptional activation of IFN-stimulated genes (ISG) that mediate IFN biologic responses. Since then, additional evidence has established critical roles for other receptor-activated signaling pathways in the induction of IFN activities. These include MAPK pathways, mTOR cascades, and PKC pathways. In addition, specific miRNAs appear to play a significant role in the regulation of IFN signaling responses. This review focuses on the emerging evidence for a model in which IFNs share signaling elements and pathways with growth factors and tumorigenic signals but engage them in a distinctive manner to mediate antiproliferative and antiviral responses.
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U2 - 10.1158/1541-7786.MCR-14-0450
DO - 10.1158/1541-7786.MCR-14-0450
M3 - Article
C2 - 25217450
AN - SCOPUS:84919341177
SN - 1541-7786
VL - 12
SP - 1691
EP - 1703
JO - Cell Growth and Differentiation
JF - Cell Growth and Differentiation
IS - 12
ER -