Evidence map›Paper›PMID 34423310›Full record

ArticleNature cancer2021

Multi-omics reveals clinically relevant proliferative drive associated with mTOR-MYC-OXPHOS activity in chronic lymphocytic leukemia.

Junyan Lu, Ester Cannizzaro, Fabienne Meier-Abt, Sebastian Scheinost, Peter-Martin Bruch, Holly Ar Giles, Almut Lütge, Jennifer Hüllein, Lena Wagner, Brian Giacopelli and 13 more

Abstract read
In one paragraph

Article in Nature cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing 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

44 citing papers in PubMed.

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  13. PD-1 expression identifies proliferating malignant CLL B cells and is a potential biomarker of response to BTK inhibitor therapy.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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

23 authors.

Junyan Lu *European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Ester Cannizzaro *Department of Medical Oncology and Hematology, University Hospital Zürich and University of Zürich, Zürich, Switzerland.
Fabienne Meier-AbtDepartment of Medical Oncology and Hematology, University Hospital Zürich and University of Zürich, Zürich, Switzerland.
Sebastian ScheinostMolecular Therapy in Hematology and Oncology, National Center for Tumor Diseases and German Cancer Research Centre, Heidelberg, Germany.
Peter-Martin BruchMolecular Therapy in Hematology and Oncology, National Center for Tumor Diseases and German Cancer Research Centre, Heidelberg, Germany.
Holly Ar GilesEuropean Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Almut LütgeDepartment of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Jennifer HülleinEuropean Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Lena WagnerMolecular Therapy in Hematology and Oncology, National Center for Tumor Diseases and German Cancer Research Centre, Heidelberg, Germany.
Brian GiacopelliDivision of Hematology, Department of Internal Medicine, The Ohio State University, Columbus, OH.
Ferran NadeuInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Julio DelgadoCentro de Investigación Biomédica en Red de Cáncer (CIBERONC), Madrid, Spain.
Elías CampoInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Maurizio MangoliniWellcome Trust/MRC Cambridge Stem Cell Institute & Department of Haematology, University of Cambridge, Cambridge CB2 0AH, UK.
Ingo RingshausenWellcome Trust/MRC Cambridge Stem Cell Institute & Department of Haematology, University of Cambridge, Cambridge CB2 0AH, UK.
Martin BöttcherDepartment of Internal Medicine 5, Hematology and Oncology, University of Erlangen-Nuremberg, Erlangen, Germany.
Dimitrios MougiakakosDepartment of Internal Medicine 5, Hematology and Oncology, University of Erlangen-Nuremberg, Erlangen, Germany.
Andrea JacobsInstitute of Molecular Health Sciences, ETH Zurich, Zurich, Switzerland.
Bernd BodenmillerInstitute of Molecular Health Sciences, ETH Zurich, Zurich, Switzerland.
Sascha DietrichMolecular Medicine Partnership Unit (MMPU), Heidelberg, Germany.
Christopher C OakesDivision of Hematology, Department of Internal Medicine, The Ohio State University, Columbus, OH.
Thorsten ZenzDepartment of Medical Oncology and Hematology, University Hospital Zürich and University of Zürich, Zürich, Switzerland.
Wolfgang HuberEuropean Molecular Biology Laboratory (EMBL), Heidelberg, Germany.

Funding

Cancer Research UK 17480Medical Research Council MC_PC_17230
6 · The paper itself

Abstract

Chronic Lymphocytic Leukemia (CLL) has a complex pattern of driver mutations and much of its clinical diversity remains unexplained. We devised a method for simultaneous subgroup discovery across multiple data types and applied it to genomic, transcriptomic, DNA methylation and ex-vivo drug response data from 217 Chronic Lymphocytic Leukemia (CLL) cases. We uncovered a biological axis of heterogeneity strongly associated with clinical behavior and orthogonal to the known biomarkers. We validated its presence and clinical relevance in four independent cohorts (

Indexed as

Leukemia, Lymphocytic, Chronic, B-CellDNA MethylationHumansOxidative PhosphorylationProteomicsTOR Serine-Threonine KinasesMTOR protein, humanTOR Serine-Threonine Kinases

Identifiers

PMID34423310
PMCPMC7611543

What OpenQuestion holds

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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.