Evidence map›Paper›PMID 41389200›Full record

ArticleCell reports2025

Ribosomal protein control of hematopoietic stem cell transformation through regulation of metabolism.

Bryan Harris, Dinesh K Singh, Billy Truong, Michele Rhodes, Rachael Price, Susan Shinton, Monika Verma, Bridget Aylward, Shawn P Fahl, Shanna R Sprinkle and 20 more

Abstract read
In one paragraph

Article in Cell reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors.

Bryan HarrisNuclear Dynamics and Cancer Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Dinesh K SinghNuclear Dynamics and Cancer Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Billy TruongNuclear Dynamics and Cancer Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Michele RhodesNuclear Dynamics and Cancer Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Rachael PriceNuclear Dynamics and Cancer Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Susan ShintonNuclear Dynamics and Cancer Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Monika VermaNuclear Dynamics and Cancer Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Bridget AylwardNuclear Dynamics and Cancer Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Shawn P FahlNuclear Dynamics and Cancer Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Shanna R SprinkleDepartment of Surgery, Duke University Medical Center, Durham, NC 27710, USA; Department of Biostatistics, University of North Carolina, Chapel Hill, Chapel Hill, NC 27599, USA.
Sarah AminovDepartment of Oncology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY 10461, USA.
Minshi WangNuclear Dynamics and Cancer Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Yong ZhangNuclear Dynamics and Cancer Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Jaqueline PerrigoueNuclear Dynamics and Cancer Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Rachel KesselDepartment of Oncology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY 10461, USA.
Suraj PeriBiostatistics and Bioinformatics Facility, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Joshua WestDepartment of Pharmacology, University of Michigan, Ann Arbor, MI, USA; Department of Internal Medicine, Division of Cardiovascular Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
Orsi GiriczDepartment of Oncology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY 10461, USA.
Jacqueline BoultwoodLLR Molecular Haematology Unit, NDCLS, John Radcliffe Hospital, and NIHR Biomedical Research Centre, Oxford OX3 9DU, UK.
Andrea PellagattiLLR Molecular Haematology Unit, NDCLS, John Radcliffe Hospital, and NIHR Biomedical Research Centre, Oxford OX3 9DU, UK.
K H RameshDepartment of Oncology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY 10461, USA.
Cristina MontagnaDepartment of Oncology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY 10461, USA.
Kith PradhanDepartment of Oncology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY 10461, USA.
Jeffrey W TynerDivision of Hematology and Medical Oncology, Oregon Health & Science University Knight Cancer Institute, Portland, OR 97239, USA.
Brian K KennedyDepartments of Biochemistry and Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597, Singapore.
Michael HolinstatDepartment of Pharmacology, University of Michigan, Ann Arbor, MI, USA; Department of Internal Medicine, Division of Cardiovascular Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
Ulrich SteidlDepartment of Oncology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY 10461, USA.
Stephen SykesDepartment of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA.
Amit VermaDepartment of Oncology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY 10461, USA.
David L WiestNuclear Dynamics and Cancer Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA. Electronic address: david.wiest@fccc.edu.

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI DAVID L. WIEST · 1985 to 2026
$138.8M
Tumor Intrinsic and Microenvironmental Mechanisms Driving Drug Combination Efficacy and Resistance in AMLU54CA224019 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Jeffrey Wallace Tyner · 2017 to 2026
$13.9M
Regulation of hematopoiesis by ribosomal protein paralogsR37AI110985 · NIAID · RESEARCH INST OF FOX CHASE CAN CTR · PI DAVID L. WIEST · 2020 to 2026
$4.2M
NCI NIH HHS P30 CA006927NCI NIH HHS U54 CA224019NIAID NIH HHS R37 AI110985
6 · The paper itself

Abstract

We report here that expression of the ribosomal protein RPL22 is frequently reduced in human myelodysplastic syndrome (MDS) and acute myelogenous leukemia (AML), and reduced RPL22 expression is associated with worse outcomes. Mice null for Rpl22 display characteristics of an MDS-like syndrome and develop leukemia at an accelerated rate. Rpl22-deficient mice also display enhanced hematopoietic stem cell (HSC) self-renewal and obstructed differentiation potential, which arises not from reduced protein synthesis but from altered metabolism, including increased fatty acid oxidation (FAO) and a striking induction of the stemness factor Lin28b in the resulting leukemia. Lin28b promotes a substantial increase in lipid content, upon which the survival of Rpl22-deficient leukemias depends. Altogether, these findings reveal that Rpl22 insufficiency enhances the leukemia potential of HSCs through regulation of FAO and promotes leukemogenesis through Lin28b promotion of lipid synthesis.

Indexed as

Cell Transformation, NeoplasticHematopoietic Stem CellsRibosomal ProteinsAnimalsCell DifferentiationFatty AcidsHumansLeukemia, Myeloid, AcuteLipid MetabolismMiceMice, Inbred C57BLMice, KnockoutMyelodysplastic SyndromesRNA-Binding ProteinsFatty AcidsLin28b protein, mouseRibosomal ProteinsRNA-Binding ProteinsAMLCP: cancerCP: molecular biologyfatty acid metabolismhematopoietic stem cellLin28bMDSribosomal proteinRpl22triglyceride

Identifiers

PMID41389200
PMCPMC12820725

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.