Evidence map›Paper›PMID 36259929›Full record

ArticleCancer discovery2023

A Dynamic rRNA Ribomethylome Drives Stemness in Acute Myeloid Leukemia.

Fengbiao Zhou, Nesrine Aroua, Yi Liu, Christian Rohde, Jingdong Cheng, Anna-Katharina Wirth, Daria Fijalkowska, Stefanie Göllner, Michelle Lotze, Haiyang Yun and 16 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer discovery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
5.1field-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.

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

50 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
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  6. RNA modifications in cancer and their detection: a review.Japanese journal of clinical oncology · 2026
    Review
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  10. Dual relevance ofFrontiers in oncology · 2026
    Article
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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

26 authors at 8 institutions in 1 country.

Fengbiao Zhou *Department of Internal Medicine V, Heidelberg University Hospital, Heidelberg, Germany.ORCID 0000-0002-9221-1096
Nesrine Aroua *Division of Stem Cells and Cancer, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID 0000-0002-0600-7954
Yi LiuDepartment of Internal Medicine V, Heidelberg University Hospital, Heidelberg, Germany.ORCID 0000-0002-4961-2660
Christian RohdeDepartment of Internal Medicine V, Heidelberg University Hospital, Heidelberg, Germany.ORCID 0000-0001-6778-5971
Jingdong ChengGene Center, Department of Biochemistry, University of Munich, Munich, Germany.ORCID 0000-0003-4442-377X
Anna-Katharina WirthResearch Unit Apoptosis in Hematopoietic Stem Cells (AHS), Helmholtz Center Munich, German Center for Environmental Health, Munich, Germany.ORCID 0000-0002-0138-8583
Daria FijalkowskaDivision of Proteomics of Stem Cells and Cancer, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID 0000-0002-2084-146X
Stefanie GöllnerDepartment of Internal Medicine V, Heidelberg University Hospital, Heidelberg, Germany.ORCID 0000-0002-2934-1920
Michelle LotzeDepartment of Internal Medicine V, Heidelberg University Hospital, Heidelberg, Germany.ORCID 0000-0003-2633-1767
Haiyang YunDepartment of Internal Medicine V, Heidelberg University Hospital, Heidelberg, Germany.ORCID 0000-0001-8714-205X
Xiaobing YuDepartment of Internal Medicine V, Heidelberg University Hospital, Heidelberg, Germany.ORCID 0000-0001-8634-4135
Caroline PabstDepartment of Internal Medicine V, Heidelberg University Hospital, Heidelberg, Germany.ORCID 0000-0001-9716-5909
Tim SauerDepartment of Internal Medicine V, Heidelberg University Hospital, Heidelberg, Germany.ORCID 0000-0001-5412-324X
Thomas OellerichDepartment of Medicine II, Hematology/Oncology, Goethe University, Frankfurt Am Main, Germany.ORCID 0000-0001-6570-6125
Hubert ServeDepartment of Medicine II, Hematology/Oncology, Goethe University, Frankfurt Am Main, Germany.ORCID 0000-0001-8472-5516
Christoph RölligMedical Department 1, University Hospital Dresden, Dresden, Germany.ORCID 0000-0002-3791-0548
Martin BornhäuserMedical Department 1, University Hospital Dresden, Dresden, Germany.
Christian ThiedeMedical Department 1, University Hospital Dresden, Dresden, Germany.ORCID 0000-0002-5916-3029
Claudia BaldusDepartment of Medicine II, Hematology and Oncology, University Hospital Schleswig-Holstein, Kiel, Germany.ORCID 0000-0002-0748-834X
Michaela FryeDivision of Mechanisms Regulating Gene Expression, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID 0000-0002-5636-6840
Simon RaffelDepartment of Internal Medicine V, Heidelberg University Hospital, Heidelberg, Germany.ORCID 0000-0003-4671-1097
Jeroen KrijgsveldDivision of Proteomics of Stem Cells and Cancer, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID 0000-0001-7549-9326
Irmela JeremiasResearch Unit Apoptosis in Hematopoietic Stem Cells (AHS), Helmholtz Center Munich, German Center for Environmental Health, Munich, Germany.ORCID 0000-0003-1773-7677
Roland BeckmannGene Center, Department of Biochemistry, University of Munich, Munich, Germany.ORCID 0000-0003-4291-3898
Andreas TrumppDivision of Stem Cells and Cancer, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID 0000-0002-6212-3466
Carsten Müller-TidowDepartment of Internal Medicine V, Heidelberg University Hospital, Heidelberg, Germany.ORCID 0000-0002-7166-5232
Heidelberg University · DEGerman Cancer Research Center · DEEuropean Molecular Biology Organization · DEUniversity Hospital Carl Gustav Carus · DEAmgen (Germany) · DEGoethe University Frankfurt · DEHelmholtz Zentrum München · DEUniversity Hospital Schleswig-Holstein · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development and regulation of malignant self-renewal remain unresolved issues. Here, we provide biochemical, genetic, and functional evidence that dynamics in ribosomal RNA (rRNA) 2'-O-methylation regulate leukemia stem cell (LSC) activity in vivo. A comprehensive analysis of the rRNA 2'-O-methylation landscape of 94 patients with acute myeloid leukemia (AML) revealed dynamic 2'-O-methylation specifically at exterior sites of ribosomes. The rRNA 2'-O-methylation pattern is closely associated with AML development stage and LSC gene expression signature. Forced expression of the 2'-O-methyltransferase fibrillarin (FBL) induced an AML stem cell phenotype and enabled engraftment of non-LSC leukemia cells in NSG mice. Enhanced 2'-O-methylation redirected the ribosome translation program toward amino acid transporter mRNAs enriched in optimal codons and subsequently increased intracellular amino acid levels. Methylation at the single site 18S-guanosine 1447 was instrumental for LSC activity. Collectively, our work demonstrates that dynamic 2'-O-methylation at specific sites on rRNAs shifts translational preferences and controls AML LSC self-renewal. SIGNIFICANCE: We establish the complete rRNA 2'-O-methylation landscape in human AML. Plasticity of rRNA 2'-O-methylation shifts protein translation toward an LSC phenotype. This dynamic process constitutes a novel concept of how cancers reprogram cell fate and function. This article is highlighted in the In This Issue feature, p. 247.

Indexed as

Leukemia, Myeloid, AcuteRNA, RibosomalAnimalsHumansMethylationMiceNeoplastic Stem CellsPhenotypeRibosomesRNA, Ribosomal

Identifiers

PMID36259929
PMCPMC9900322
OpenAlexW4306793037

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.