Evidence map›Paper›PMID 36719747›Full record

ArticleThe Journal of clinical investigation2023

Targeting pleckstrin-2/Akt signaling reduces proliferation in myeloproliferative neoplasm models.

Xu Han, Yang Mei, Rama K Mishra, Honghao Bi, Atul D Jain, Gary E Schiltz, Baobing Zhao, Madina Sukhanova, Pan Wang, Arabela A Grigorescu and 9 more

Open access · goldFull text read
In one paragraph

Article in The Journal of clinical investigation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

19 authors at 7 institutions in 3 countries.

Xu HanDepartment of Pathology, Feinberg School of Medicine.
Yang MeiDepartment of Pathology, Feinberg School of Medicine.
Rama K MishraDepartment of Biochemistry and Molecular Genetics, Feinberg School of Medicine.
Honghao BiDepartment of Pathology, Feinberg School of Medicine.
Atul D JainDepartment of Chemistry, and.
Gary E SchiltzRobert H. Lurie Comprehensive Cancer Center.
Baobing ZhaoDepartment of Pathology, Feinberg School of Medicine.
Madina SukhanovaDepartment of Pathology, Feinberg School of Medicine.
Pan WangDepartment of Pathology, Feinberg School of Medicine.
Arabela A GrigorescuDepartment of Molecular Biosciences, Weinberg College of Arts & Sciences, Northwestern University, Evanston, Illinois, USA.
Patricia C WeberHarrington Discovery Institute, Cleveland, Ohio, USA.
John J PiwinskiHarrington Discovery Institute, Cleveland, Ohio, USA.
Miguel A PradoDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts, USA.
Joao A PauloDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts, USA.
Len StephensSignaling Programme, The Babraham Institute, Cambridge, United Kingdom.
Karen E AndersonSignaling Programme, The Babraham Institute, Cambridge, United Kingdom.
Charles S AbramsDepartment of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Jing YangDepartment of Pathology, Feinberg School of Medicine.
Peng JiDepartment of Pathology, Feinberg School of Medicine.
Weinberg Medical Physics (United States) · USBabraham Institute · GBHarvard University · USNorthwestern University · USOhio Aerospace Institute · USInstitut thématique Génétique, génomique et bioinformatique · FRUniversity of Pennsylvania · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LEONIDAS C. PLATANIAS · 1993 to 2026
$153.9M
Studies of Physiologic and Pathologic Platelet Plug FormationP01HL146373 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI BRASS, LAWRENCE F · 2020 to 2024
$12.2M
The Novel Mechanisms of Thrombosis Formation in Myeloproliferative DiseasesR01HL148014 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI ABRAMS, CHARLES S. · 2020 to 2023
$2.5M
Targeting gasdermin D to treat myelodysplastic syndromesR01HL169507 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Peng Ji · 2023 to 2026
$2.1M
The roles of mDia2 in hematopoietic stem and progenitor cell engraftment and migrationR01HL148012 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JI, PENG · 2020 to 2023
$2.1M
The roles of mDia2 in membrane remodeling and organelle clearance during reticulocyte formationR01DK124220 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JI, PENG · 2020 to 2024
$2.0M
The role of Pleckstrin-2 as a functional node in myeloid proliferationR01HL150729 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JI, PENG · 2020 to 2023
$2.0M
Developing small molecule inhibitors of Pleckstrin-2 to treat thrombosisR43HL165997 · NHLBI · APLEXIS, INC. · PI YANG, JING · 2022 to 2022
$397k
Biotechnology and Biological Sciences Research Council BBS/E/B/000C0413Biotechnology and Biological Sciences Research Council BBS/E/B/000C0415NCI NIH HHS P30 CA060553NHLBI NIH HHS P01 HL146373NHLBI NIH HHS R01 HL148012NHLBI NIH HHS R01 HL148014NHLBI NIH HHS R01 HL150729NHLBI NIH HHS R01 HL169507NHLBI NIH HHS R43 HL165997NIDDK NIH HHS R01 DK124220
6 · The paper itself

Abstract

Myeloproliferative neoplasms (MPNs) are characterized by the activated JAK2/STAT pathway. Pleckstrin-2 (Plek2) is a downstream target of the JAK2/STAT5 pathway and is overexpressed in patients with MPNs. We previously revealed that Plek2 plays critical roles in the pathogenesis of JAK2-mutated MPNs. The nonessential roles of Plek2 under physiologic conditions make it an ideal target for MPN therapy. Here, we identified first-in-class Plek2 inhibitors through an in silico high-throughput screening approach and cell-based assays, followed by the synthesis of analogs. Plek2-specific small-molecule inhibitors showed potent inhibitory effects on cell proliferation. Mechanistically, Plek2 interacts with and enhances the activity of Akt through the recruitment of downstream effector proteins. The Plek2-signaling complex also includes Hsp72, which protects Akt from degradation. These functions were blocked by Plek2 inhibitors via their direct binding to the Plek2 dishevelled, Egl-10 and pleckstrin (DEP) domain. The role of Plek2 in activating Akt signaling was further confirmed in vivo using a hematopoietic-specific Pten-knockout mouse model. We next tested Plek2 inhibitors alone or in combination with an Akt inhibitor in various MPN mouse models, which showed significant therapeutic efficacies similar to that seen with the genetic depletion of Plek2. The Plek2 inhibitor was also effective in reducing proliferation of CD34-positive cells from MPN patients. Our studies reveal a Plek2/Akt complex that drives cell proliferation and can be targeted by a class of antiproliferative compounds for MPN therapy.

Indexed as

Myeloproliferative DisordersNeoplasmsAnimalsBlood ProteinsCell ProliferationJanus Kinase 2MicePhosphoproteinsProto-Oncogene Proteins c-aktSignal TransductionBlood ProteinsJanus Kinase 2Phosphoproteinsplatelet protein P47Proto-Oncogene Proteins c-aktBone marrowCancerDrug screensHematologyOncology

Identifiers

PMID36719747
PMCPMC10014099
OpenAlexW4318671083

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read70
identifiers read1
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.