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Updated: May 11, 2026

A Method for Screening and Validation of Resistant Mutations Against Kinase Inhibitors
Published on: December 7, 2014
Sensitivity and resistance of JAK2 inhibitors to myeloproliferative neoplasms
Neha Bhagwat1, Ross L Levine, Priya Koppikar
1Human Oncology and Pathogenesis Program, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, USA.
Abstract:
The discovery of activating mutations in JAK2 and MPL in a majority of patients with myeloproliferative neoplasms (MPN) has led to the rapid clinical development of several JAK kinase inhibitors. Of these, the JAK1/2 inhibitor, ruxolitinib (INCB018424, Incyte Corporation) was recently approved for the treatment of patients with myelofibrosis (MF). JAK inhibitors have effectively reduced splenomegaly and high cytokine levels in patients leading to improvements in quality of life. However, they have not been successful in eliminating the mutant clone in a majority of patients. In vitro studies using saturation mutagenesis screens have revealed several mutations in JAK2 that confer resistance to JAK inhibitors. Nevertheless, these mutations have not been identified so far in JAK inhibitor-treated patients. A recent study from our laboratory demonstrated that chronic JAK kinase inhibition leads to JAK inhibitor persistence via transphosphorylation of JAK2 through other JAK kinase family members. This phenomenon is seen in cell lines, mouse models and patient samples. The JAK inhibitor persistent cells, however, still remain JAK2 dependent and therefore combination therapies that target JAK2 and other components of the JAK-STAT pathway along with JAK inhibitors may provide additional benefits and improve clinical outcomes in these patients.
Insights
JAK inhibitors treat myeloproliferative neoplasms but do not eliminate the disease. Chronic inhibition causes JAK inhibitor persistence, suggesting combination therapies targeting JAK2 may improve outcomes.
Area of Science:
- Hematology
- Molecular Biology
- Oncology
Background:
- Activating mutations in JAK2 and MPL are common in myeloproliferative neoplasms (MPNs).
- JAK kinase inhibitors, such as ruxolitinib, are approved for myelofibrosis (MF) and improve symptoms.
- Current JAK inhibitors do not eliminate the underlying mutant clone in most patients.
Purpose of the Study:
- To investigate mechanisms of JAK inhibitor resistance in MPNs.
- To explore combination therapy strategies for improved clinical outcomes.
Main Methods:
- Saturation mutagenesis screens to identify JAK2 resistance mutations.
- In vitro and in vivo studies (cell lines, mouse models) to assess JAK inhibitor persistence.
- Analysis of patient samples.
Main Results:
- JAK inhibitor resistance mutations in JAK2 have not been identified in treated patients.
- Chronic JAK kinase inhibition leads to JAK inhibitor persistence through JAK2 transphosphorylation by other JAK family members.
- This phenomenon was observed in cell lines, mouse models, and patient samples.
Conclusions:
- JAK inhibitor persistence is a mechanism of resistance in MPNs.
- Persistent cells remain dependent on JAK2, suggesting combination therapies targeting JAK2 and other JAK-STAT pathway components may be beneficial.
- Targeted combination therapies could improve clinical outcomes for MPN patients.
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