Evidence map›Paper›PMID 33500244›Full record

ArticleCancer discovery2021

Chemotherapy Induces Senescence-Like Resilient Cells Capable of Initiating AML Recurrence.

Cihangir Duy, Meng Li, Matt Teater, Cem Meydan, Francine E Garrett-Bakelman, Tak C Lee, Christopher R Chin, Ceyda Durmaz, Kimihito C Kawabata, Eugen Dhimolea and 8 more

Open access · greenAbstract read
In one paragraph

Article in Cancer discovery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 162 papers.

0numbers the graph read from it
0cells of the map it votes in
162citing papers in PubMed
24.9field-weighted citation impact, top 1% 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

162 citing papers in PubMed, 246 citations in OpenAlex.

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  16. Stochasticity in mammalian cell growth rates drives cell-to-cell variability independently of cell size and divisions.Proceedings of the National Academy of Sciences of the United States of America · 2026
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102 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

18 authors at 8 institutions in 3 countries.

Cihangir DuyCancer Signaling and Epigenetics Program, Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania. amm2014@med.cornell.edu cihangir.duy@fccc.edu.
Meng LiDepartment of Medicine, Division of Hematology and Oncology, Weill Cornell Medicine, New York, New York.
Matt TeaterDepartment of Medicine, Division of Hematology and Oncology, Weill Cornell Medicine, New York, New York.ORCID 0000-0001-9415-1659
Cem MeydanDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, New York.ORCID 0000-0002-0663-6216
Francine E Garrett-BakelmanDepartment of Medicine, Division of Hematology and Oncology, Weill Cornell Medicine, New York, New York.ORCID 0000-0002-4771-628X
Tak C LeeDepartment of Medicine, Division of Hematology and Oncology, Weill Cornell Medicine, New York, New York.
Christopher R ChinDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, New York.ORCID 0000-0002-2140-3197
Ceyda DurmazDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, New York.
Kimihito C KawabataDepartment of Medicine, Division of Hematology and Oncology, Weill Cornell Medicine, New York, New York.
Eugen DhimoleaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Constantine S MitsiadesDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Hartmut DoehnerUniversitätsklinikum Ulm, Ulm, Germany.
Richard J D'AndreaUniversity of South Australia, Adelaide, Australia.
Michael W BeckerUniversity of Rochester Medical Center, Rochester, New York.
Elisabeth M PaiettaOncology, Montefiore Medical Center, Bronx, New York.
Christopher E MasonDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, New York.ORCID 0000-0002-1850-1642
Martin CarrollUniversity of Pennsylvania, Philadelphia, Pennsylvania.
Ari M MelnickDepartment of Medicine, Division of Hematology and Oncology, Weill Cornell Medicine, New York, New York. amm2014@med.cornell.edu cihangir.duy@fccc.edu.ORCID 0000-0002-8074-2287
Cornell University · USBroad Institute · USFox Chase Cancer Center · USMontefiore Medical Center · USUniversität Ulm · DEUniversity of Pennsylvania · USUniversity of Rochester Medical Center · USUniversity of South Australia · AU

Funding

Project-006U10CA180820 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI Peter J ODwyer · 2014 to 2026
$167.6M
ECOG-ACRIN Biospecimen Bank to Support NCTNU24CA196172 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI STANLEY R. HAMILTON, Scott D Jewell · 2015 to 2026
$41.1M
Targeting Epigenetic Circuits in B-Cell LymphomasR35CA220499 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI MELNICK, ARI M. · 2018 to 2024
$7.2M
ECOG-ACRIN Integrated Leukemia Translational Science Center (LTSC)UG1CA233332 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI CAI, SHENG, LEVINE, ROSS L · 2019 to 2025
$6.2M
Role of Cytokines in Myeloma PathogenesisR01CA050947 · NCI · DANA-FARBER CANCER INSTITUTE · PI ANDERSON, KENNETH C., MITSIADES, CONSTANTINE S. · 1991 to 2018
$5.1M
Understanding and Targeting Chemotherapy Resistance in Acute Myeloid LeukemiaR01CA198089 · NCI · UNIVERSITY OF PENNSYLVANIA · PI CARROLL, MARTIN · 2015 to 2019
$3.3M
Analysis of E-selectin Ligands of Human Acute Leukemia Cells and their Biology in LeukemogenesisU01CA225730 · NCI · FLORIDA INTERNATIONAL UNIVERSITY · PI MITSIADES, CONSTANTINE S., SACKSTEIN, ROBERT · 2019 to 2023
$3.0M
ECOG-ACRIN INTEGRATED LEUKEMIA TRANSLATIONAL RESEARCH CENTERU10CA180827 · NCI · MONTEFIORE MEDICAL CENTER (BRONX, NY) · PI LEVINE, ROSS L, MELNICK, ARI M. · 2014 to 2018
$3.0M
Humanized bone marrow-like model to study patient-derived myeloma xenograftsR01CA196664 · NCI · DANA-FARBER CANCER INST · PI GROEN, RICHARD, MITSIADES, CONSTANTINE S. · 2016 to 2018
$1.6M
Genetic and epigenetic basis of relapse in acute myeloid leukemiaK08CA169055 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI GARRETT-BAKELMAN, FRANCINE EVALINA · 2012 to 2016
$742k
NCI NIH HHS K08 CA169055NCI NIH HHS R01 CA050947NCI NIH HHS R01 CA196664NCI NIH HHS R01 CA198089NCI NIH HHS R35 CA220499NCI NIH HHS U01 CA225730NCI NIH HHS U10 CA180820NCI NIH HHS U10 CA180827NCI NIH HHS U24 CA196172NCI NIH HHS UG1 CA233332
6 · The paper itself

Abstract

Patients with acute myeloid leukemia (AML) frequently relapse after chemotherapy, yet the mechanism by which AML reemerges is not fully understood. Herein, we show that primary AML cells enter a senescence-like phenotype following chemotherapy

Indexed as

Remission InductionAnimalsCell Line, TumorHumansLeukemia, Myeloid, AcuteMiceMice, Inbred NODNeoplasm Recurrence, LocalNeoplastic Stem CellsPhenotype

Identifiers

PMID33500244
PMCPMC8178167
OpenAlexW3124870698

What OpenQuestion holds

Textmetadata
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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.