Evidence map›Paper›PMID 34642468›Full record

ArticleLeukemia2022

Combined Drug Targeting of p53-dependent and -independent Pathways Depletes Myelofibrosis Hematopoietic Stem/Progenitor Cells.

Min Lu, Lijuan Xia, Nada Elmansy, Cara Clementelli, Douglas Tremblay, Ronald Hoffman

Open access · hybridAbstract read
In one paragraph

Article in Leukemia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

5 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Unraveling the role ofHemaSphere · 2026
    Review
  5. Article
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

6 authors at 1 institution in 1 country.

Min LuDivision of Hematology/Oncology, Tisch Cancer Institute and Department of Medicine, Myeloproliferative Neoplasm-Research Consortium, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA.
Lijuan XiaDivision of Hematology/Oncology, Tisch Cancer Institute and Department of Medicine, Myeloproliferative Neoplasm-Research Consortium, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA.
Nada ElmansyDivision of Hematology/Oncology, Tisch Cancer Institute and Department of Medicine, Myeloproliferative Neoplasm-Research Consortium, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA.
Cara ClementelliDivision of Hematology/Oncology, Tisch Cancer Institute and Department of Medicine, Myeloproliferative Neoplasm-Research Consortium, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA.
Douglas TremblayDivision of Hematology/Oncology, Tisch Cancer Institute and Department of Medicine, Myeloproliferative Neoplasm-Research Consortium, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA.
Ronald HoffmanDivision of Hematology/Oncology, Tisch Cancer Institute and Department of Medicine, Myeloproliferative Neoplasm-Research Consortium, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA. ronald.hoffman@mssm.edu.ORCID http://orcid.org/0000-0001-6564-6732
Tisch Hospital · US

Funding

Tissue BankP01CA108671 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Ronald Hoffman · 2006 to 2026
$82.0M
NCI NIH HHS P01 CA108671
6 · The paper itself

Abstract

Current therapy for myelofibrosis (MF) results in a limited prolongation of patient survival. In order to improve treatment outcomes, we developed a strategy to effectively deplete MF hematopoietic stem/progenitor cells (HSPCs). In the present study, an imipridone, ONC201, was combined with RG7112, an antagonist of MDM2, a p53 negative regulator, to activate downstream events of the p53 and TNF-related apoptosis-inducing ligand (TRAIL)/death receptor (DR) pathways. As compared to treatment with the individual drugs, the combination of ONC201 and RG7112 promoted greater degrees of apoptosis of MF CD34

Indexed as

Antineoplastic AgentsCells, CulturedDrug Delivery SystemsHematopoietic Stem CellsHumansImidazolesImidazolinesPrimary MyelofibrosisPyridinesPyrimidinesSignal TransductionTumor Suppressor Protein p53Antineoplastic AgentsImidazolesImidazolinesPyridinesPyrimidinesRG7112TIC10 compoundTumor Suppressor Protein p53

Identifiers

PMID34642468
PMCPMC8885407
OpenAlexW3206777006

What OpenQuestion holds

Textmetadata
LicenceTDM
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.