Gene interactions and pathways from curated databases and text-mining

◀ Back to MYC

JAK2 — MYC

Pathways - manually collected, often from reviews:

Text-mined interactions from Literome

Xie et al., Oncogene 2002 (Leukemia, Myelogenous, Chronic, BCR-ABL Positive) : Jak2 is involved in c-Myc induction by Bcr-Abl ... Since the Jak2 binds to the C-terminal domain of Bcr-Abl and optimal Jak2 activation requires the SH2 domain, we tested whether Jak2 was involved in c-Myc protein induction by Bcr-Abl ... In summary, our findings indicate that Jak2 mediates the increase in c-Myc expression that is induced by Bcr-Abl ... Our results indicate that activated Jak2 not only mediates an increase of c-MYC RNA expression but also interferes with proteasome dependent degradation of c-Myc protein
Samanta et al., Cancer Res 2006 (Leukemia, Myelogenous, Chronic, BCR-ABL Positive) : Similar to wild-type Bcr-Abl+ cells, inhibition of Jak2 by Ag490 treatment resulted in decrease of pSer Akt and c-Myc in imatinib-resistant cells
Konforte et al., J Immunol 2006 : Our study is the first to show the link between IL-21 induced JAK/STAT signaling, c-Myc regulation , and differentiation of human B cells
Lee et al., J Cell Biochem 2009 : JAK pathway induction of c-Myc critical to IL-5 stimulation of cell proliferation and inhibition of apoptosis ... We further examined the role of JAK1 and JAK2 in the induction of c-Myc expression using the CDJAK fusion proteins, which consisted of a CD16 extracellular domain, a CD7 transmembrane domain, and either JAK1 ( CDJAK1 ) or JAK2 ( CDJAK2 ) as intracellular domains ... Simultaneous activation of JAK1 and JAK2 by anti-CD16 antibody crosslinking of CDJAK1 and CDJAK2 could induced c-Myc expression and promoter activity ; AG490 inhibited CDJAK1 and CDJAK2 mediated effects
Li et al., PloS one 2012 (Hypereosinophilic Syndrome) : Interestingly, JAK2 inhibition also reduced PI3K, Akt and NF-?B activity in a dose dependent manner, and suppressed expression levels of c-Myc and Survivin ... Interestingly, JAK2 inhibition also reduced PI3K, Akt and NF-?B activity in a dose dependent manner, and suppressed expression levels of c-Myc and Survivin