Mark Soto

ORCID: 0000-0001-9996-9003
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Chronic Myeloid Leukemia Treatments
  • Eosinophilic Disorders and Syndromes
  • Acute Myeloid Leukemia Research
  • Kruppel-like factors research

Albert Einstein College of Medicine
2022

Abstract Purpose: The Philadelphia chromosome–negative myeloproliferative neoplasms (MPN) polycythemia vera, essential thrombocythemia, and primary myelofibrosis are characterized by JAK/STAT pathway activation. JAK inhibitors approved for MPN treatment, but persistence has been observed, due to reactivation. Experimental Design: Using patient samples, JAK2-mutated cell lines, mouse models, we examined both the efficacy mechanism which crizotinib, ALK/MET/RON/ROS1 inhibitor treatment of...

10.1158/1078-0432.ccr-22-1763 article EN Clinical Cancer Research 2022-12-20

<div>AbstractPurpose:<p>The Philadelphia chromosome–negative myeloproliferative neoplasms (MPN) polycythemia vera, essential thrombocythemia, and primary myelofibrosis are characterized by JAK/STAT pathway activation. JAK inhibitors approved for MPN treatment, but persistence has been observed, due to reactivation.</p>Experimental Design:<p>Using patient samples, JAK2-mutated cell lines, mouse models, we examined both the efficacy mechanism which crizotinib,...

10.1158/1078-0432.c.6533203 preprint EN 2023-04-01

<div>AbstractPurpose:<p>The Philadelphia chromosome–negative myeloproliferative neoplasms (MPN) polycythemia vera, essential thrombocythemia, and primary myelofibrosis are characterized by JAK/STAT pathway activation. JAK inhibitors approved for MPN treatment, but persistence has been observed, due to reactivation.</p>Experimental Design:<p>Using patient samples, JAK2-mutated cell lines, mouse models, we examined both the efficacy mechanism which crizotinib,...

10.1158/1078-0432.c.6533203.v1 preprint EN 2023-04-01
Coming Soon ...