Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:3.5.1.1 (
asparaginase
)
2,695
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The poor outcomes in infant acute lymphoblastic leukemia (ALL) necessitate new treatments. Here we discover that
EIF4E
protein is elevated in most cases of infant ALL and test
EIF4E
targeting by the repurposed antiviral agent ribavirin, which has anticancer properties through
EIF4E
inhibition, as a potential treatment. We find that ribavirin treatment of actively dividing infant ALL cells on bone marrow stromal cells (BMSCs) at clinically achievable concentrations causes robust proliferation inhibition in proportion with
EIF4E
expression. Further, we find that ribavirin treatment of KMT2A-rearranged (KMT2A-R) infant ALL cells and the KMT2A-AFF1 cell line RS4:11 inhibits
EIF4E
, leading to decreases in oncogenic
EIF4E
-regulated cell growth and survival proteins. In ribavirin-sensitive KMT2A-R infant ALL cells and RS4:11 cells,
EIF4E
-regulated proteins with reduced levels of expression following ribavirin treatment include MYC, MCL1, NBN, BCL2 and BIRC5. Ribavirin-treated RS4:11 cells exhibit impaired
EIF4E
-dependent nuclear to cytoplasmic export and/or translation of the corresponding mRNAs, as well as reduced phosphorylation of the p-AKT1, p-EIF4EBP1, p-RPS6 and p-
EIF4E
signaling proteins. This leads to an S-phase cell cycle arrest in RS4:11 cells corresponding to the decreased proliferation. Ribavirin causes nuclear
EIF4E
to re-localize to the cytoplasm in KMT2A-AFF1 infant ALL and RS4:11 cells, providing further evidence for
EIF4E
inhibition. Ribavirin slows increases in peripheral blasts in KMT2A-R infant ALL xenograft-bearing mice. Ribavirin cooperates with chemotherapy, particularly
L-asparaginase
, in reducing live KMT2A-AFF1 infant ALL cells in BMSC co-cultures. This work establishes that
EIF4E
is broadly elevated across infant ALL and that clinically relevant ribavirin exposures have preclinical activity and effectively inhibit
EIF4E
in KMT2A-R cases, suggesting promise in
EIF4E
targeting using ribavirin as a means of treatment.
...
PMID:Targeting EIF4E signaling with ribavirin in infant acute lymphoblastic leukemia. 3047 48