Evidence map›Paper›PMID 28126925›Full record

ArticleBlood2017

MUC1-mediated induction of myeloid-derived suppressor cells in patients with acute myeloid leukemia.

Athalia Rachel Pyzer, Dina Stroopinsky, Hasan Rajabi, Abigail Washington, Ashujit Tagde, Maxwell Coll, Jacqueline Fung, Mary Paty Bryant, Leandra Cole, Kristen Palmer and 14 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Blood, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07511062 (Axatilimab Combined With Decitabine/Venetoclax for the Treatment of TP53-mutated/Deleted AML Patients), which is not on this map. Cited by 120 papers.

0numbers the graph read from it
0cells of the map it votes in
120citing papers in PubMed
6.1field-weighted citation impact, top 3% 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.

NCT07511062 phase1not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Axatilimab Combined With Decitabine/Venetoclax for the Treatment of TP53-mutated/Deleted AML Patients

TypeinterventionalSponsorNorthside Hospital, Inc.Ran2026 to 2030Enrolled32ConditionsAcute Myeloid Leukemia, TP53 Gene MutationArmsDecitabine, Venetoclax, Axatilimab
3 · Its place in the literature

Who cites it

120 citing papers in PubMed, 190 citations in OpenAlex.

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  14. Shared genetic association between inflammatory bowel disease and acute myeloid leukemia: insights from mendelian randomization and transcriptomic analyses.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
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60 more citing papers are in PubMed but not listed here.

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

24 authors at 2 institutions in 1 country.

Athalia Rachel PyzerDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.ORCID http://orcid.org/0000-0002-0506-1887
Dina StroopinskyDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
Hasan RajabiDana Farber Cancer Institute, and.
Abigail WashingtonDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
Ashujit TagdeDana Farber Cancer Institute, and.
Maxwell CollDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
Jacqueline FungCancer Genetics Program, Beth Israel Deaconess Cancer Center, Harvard Medical School, Boston, MA.
Mary Paty BryantDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
Leandra ColeDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
Kristen PalmerDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
Poorvi SomaiyaDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
Rebecca Karp LeafDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
Myrna NahasDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
Arie ApelDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
Salvia JainDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
Malgorzata McMastersDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
Lourdes MendezDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
James LevineDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
Robin JoyceDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
Jon ArnasonDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
Pier Paolo PandolfiCancer Genetics Program, Beth Israel Deaconess Cancer Center, Harvard Medical School, Boston, MA.
Donald KufeDana Farber Cancer Institute, and.
Jacalyn RosenblattDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
David AviganDepartment of Bone Marrow Transplantation, Beth Israel Deaconess Medical Center.
Dana-Farber Cancer Institute · USBeth Israel Deaconess Medical Center · US

Funding

Trageting the Multiple Myeloma EpigenomeP50CA100707 · NCI · DANA-FARBER CANCER INSTITUTE · PI ANDERSON, KENNETH C., MUNSHI, NIKHIL C. · 2003 to 2023
$45.0M
Targeting Genomic Instability and Evolution in MyelomaP01CA155258 · NCI · DANA-FARBER CANCER INST · PI Jill Corre · 2011 to 2026
$32.5M
Targeting Myeloma Cell-Host Bone Marrow InteractionsP01CA078378 · NCI · DANA-FARBER CANCER INSTITUTE · PI RITZ, JEROME · 1998 to 2014
$26.2M
MUC1-C Oncoprotein Evades Immune Destruction in Non-small Cell Lung CancerR01CA166480 · NCI · DANA-FARBER CANCER INST · PI KUFE, DONALD W., WONG, KWOK KIN · 2012 to 2021
$6.3M
NCI NIH HHS P01 CA078378NCI NIH HHS P01 CA155258NCI NIH HHS P50 CA100707NCI NIH HHS R01 CA166480
6 · The paper itself

Abstract

Myeloid-derived suppressor cells (MDSCs) play a critical role in promoting immune tolerance and disease growth. The mechanism by which tumor cells evoke the expansion of MDSCs in acute myeloid leukemia (AML) has not been well described. We have demonstrated that patients with AML exhibit increased presence of MDSCs in their peripheral blood, in comparison with normal controls. Cytogenetic studies demonstrated that MDSCs in patients with AML may be derived from leukemic or apparently normal progenitors. Engraftment of C57BL/6 mice with TIB-49 AML led to an expansion of CD11b

Indexed as

Cell ProliferationAnimalsCell CommunicationCell Line, TumorCoculture TechniquesExtracellular VesiclesHeterograftsHumansLeukemia, Myeloid, AcuteLeukocytes, MononuclearMiceMicroRNAsMucin-1Myeloid-Derived Suppressor CellsProto-Oncogene Proteins c-mycMicroRNAsMIRN34 microRNA, humanMucin-1MYC protein, humanProto-Oncogene Proteins c-myc

Identifiers

PMID28126925
PMCPMC5813734
OpenAlexW2580571122

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.