Evidence map›Paper›PMID 36044389›Full record

ArticleBlood advances2023

Rational polypharmacological targeting of FLT3, JAK2, ABL, and ERK1 suppresses the adaptive resistance to FLT3 inhibitors in AML.

Mohammad Azhar, Zachary Kincaid, Meenu Kesarwani, Jacob Menke, Joshua Schwieterman, Sekhu Ansari, Angela Reaves, Arhama Ahmed, Rammsha Shehzad, Areeba Khan and 6 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Therapeutic targeting of p90 ribosomal S6 kinase.Frontiers in cell and developmental biology · 2023
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 2 institutions in 1 country.

Mohammad AzharDivision of Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Zachary KincaidDivision of Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Meenu KesarwaniDivision of Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Jacob MenkeDivision of Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Joshua SchwietermanDivision of Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Sekhu AnsariDivision of Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.ORCID 0000-0002-3968-5508
Angela ReavesDivision of Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Arhama AhmedDivision of Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Rammsha ShehzadDivision of Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Areeba KhanDivision of Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Nuha SyedDivision of Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Noor AmirDivision of Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Mark WunderlichDivision of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.ORCID 0000-0002-2166-5146
Tahir LatifDepartment of Internal Medicine, University of Cincinnati, Cincinnati, OH.
William SeibelDivision of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.ORCID 0000-0003-1401-8618
Mohammad AzamDivision of Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Cincinnati Children's Hospital Medical Center · USUniversity of Cincinnati · US

Funding

Mechanism of Therapy in high-risk AMLR01CA250516 · NCI · CINCINNATI CHILDRENS HOSP MED CTR · PI AZAM, MOHAMMAD · 2020 to 2024
$2.4M
Therapeutic insights through patient derived leukemia xenograftsR50CA211404 · NCI · CINCINNATI CHILDRENS HOSP MED CTR · PI Mark Wunderlich · 2016 to 2026
$1.9M
Mechanism of non-oncogene addictionR01CA211594 · NCI · CINCINNATI CHILDRENS HOSP MED CTR · PI AZAM, MOHAMMAD · 2018 to 2022
$1.8M
Target the Dusp1 in Jak2 dependent myeloproliferative neoplasm (MPN) for curative treatmentR21CA280723 · NCI · CINCINNATI CHILDRENS HOSP MED CTR · PI AZAM, MOHAMMAD · 2023 to 2024
$403k
NCI NIH HHS R01 CA211594NCI NIH HHS R01 CA250516NCI NIH HHS R21 CA280723NCI NIH HHS R50 CA211404
6 · The paper itself

Abstract

Despite significant advancements in developing selective FMS-like tyrosine kinase 3 (FLT3) inhibitors, resistance to treatment is common even on continued therapy. Acquisition of on-target mutations or adaptation to MAPK, JAK2, and ABL signaling pathways drive treatment failure and disease relapse. Although combinatorial targeting of all escape routes in preclinical models demonstrated its efficacy, the clinical application is challenging owing to drug-drug interaction and differing pharmacokinetics of the inhibitors. We reasoned that selective polypharmacological targeting could lead to a durable response with reduced toxicity. A cell-based screening was carried out to identify inhibitors targeting FLT3, RAS-MAPK, BCR-ABL, and JAK2 to target the adaptive resistance observed with FLT3 inhibitors. Here, we show that pluripotin is an equipotent inhibitor of FLT3, BCR-ABL, and JAK2 in addition to inhibiting Ras-GAP and extracellular signal-regulated kinase 1 (ERK1). Structural modeling studies revealed that pluripotin is a type II kinase inhibitor that selectively binds with inactive conformations of FLT3, ABL, and JAK2. Pluripotin showed potent inhibitory activity on both mouse and human cells expressing FLT3ITD, including clinically challenging resistant mutations of the gatekeeper residue, F691L. Likewise, pluripotin suppressed the adaptive resistance conferred by the activation of RAS-MAPK pathways, BCR-ABL, and JAK2 signaling. Treatment with pluripotin curbed the progression of acute myeloid leukemia (AML) in multiple in vivo models including patient-derived primary AML cells in mouse xenotransplants. As a proof of concept, we demonstrate that targeted polypharmacological inhibition of key signaling nodes driving adaptive resistance can provide a durable response.

Indexed as

fms-Like Tyrosine Kinase 3Leukemia, Myeloid, AcuteAnimalsHumansJanus Kinase 2MiceMitogen-Activated Protein Kinase 3Protein Kinase InhibitorsSignal TransductionFLT3 protein, humanfms-Like Tyrosine Kinase 3JAK2 protein, humanJanus Kinase 2Mitogen-Activated Protein Kinase 3Protein Kinase Inhibitors

Identifiers

PMID36044389
PMCPMC10125913
OpenAlexW4293787219

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.