Evidence map›Paper›PMID 36572751›Full record

ArticleLeukemia2023

Proteogenomic analysis of acute myeloid leukemia associates relapsed disease with reprogrammed energy metabolism both in adults and children.

Svea Stratmann, Mattias Vesterlund, Husen M Umer, Saeed Eshtad, Aron Skaftason, Morten Krogh Herlin, Christer Sundström, Anna Eriksson, Martin Höglund, Josefine Palle and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Leukemia, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
5.9field-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

26 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Localized heme sensing through a ternary molecular glue.bioRxiv : the preprint server for biology · 2026
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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

19 authors at 7 institutions in 4 countries.

Svea StratmannDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-7438-9093
Mattias VesterlundDepartment of Oncology-Pathology, Karolinska Institutet, and Science for Life Laboratory, Stockholm, Sweden.ORCID 0000-0001-9471-6592
Husen M UmerDepartment of Oncology-Pathology, Karolinska Institutet, and Science for Life Laboratory, Stockholm, Sweden.ORCID 0000-0003-3971-2462
Saeed EshtadDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Aron SkaftasonDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Morten Krogh HerlinDepartment of Clinical Medicine, Aarhus University, Aarhus, Denmark.ORCID 0000-0001-7179-4643
Christer SundströmDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-8160-5647
Anna ErikssonDepartment of Medical Sciences, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-8853-1863
Martin HöglundDepartment of Medical Sciences, Uppsala University, Uppsala, Sweden.
Josefine PalleDepartment of Women's and Children's Health, Uppsala University, Uppsala, Sweden.
Jonas AbrahamssonDepartment of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
Kirsi JahnukainenChildren's Hospital, University of Helsinki and Helsinki University Central Hospital, Helsinki, Finland.ORCID 0000-0001-9296-2028
Monica Cheng Munthe-KaasNorwegian Institute of Public Health, Oslo, Norway.
Bernward ZellerDepartment of Pediatric Oncology and Hematology, Oslo University Hospital, Oslo, Norway.
Katja Pokrovskaja TammDepartment of Oncology and Pathology, Karolinska Institutet, Bioclinicum, Solna, Sweden.ORCID 0000-0001-6359-1256
Cecilia LindskogDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Lucia CavelierDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Janne LehtiöDepartment of Oncology-Pathology, Karolinska Institutet, and Science for Life Laboratory, Stockholm, Sweden.ORCID 0000-0002-8100-9562
Linda HolmfeldtDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden. linda.holmfeldt@igp.uu.se.ORCID 0000-0003-4140-3423
Uppsala University · SEScience for Life Laboratory · SEKarolinska Institutet · SEOslo University Hospital · NOAarhus University · DKUniversity of Gothenburg · SEUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite improvement of current treatment strategies and novel targeted drugs, relapse and treatment resistance largely determine the outcome for acute myeloid leukemia (AML) patients. To identify the underlying molecular characteristics, numerous studies have been aimed to decipher the genomic- and transcriptomic landscape of AML. Nevertheless, further molecular changes allowing malignant cells to escape treatment remain to be elucidated. Mass spectrometry is a powerful tool enabling detailed insights into proteomic changes that could explain AML relapse and resistance. Here, we investigated AML samples from 47 adult and 22 pediatric patients at serial time-points during disease progression using mass spectrometry-based in-depth proteomics. We show that the proteomic profile at relapse is enriched for mitochondrial ribosomal proteins and subunits of the respiratory chain complex, indicative of reprogrammed energy metabolism from diagnosis to relapse. Further, higher levels of granzymes and lower levels of the anti-inflammatory protein CR1/CD35 suggest an inflammatory signature promoting disease progression. Finally, through a proteogenomic approach, we detected novel peptides, which present a promising repertoire in the search for biomarkers and tumor-specific druggable targets. Altogether, this study highlights the importance of proteomic studies in holistic approaches to improve treatment and survival of AML patients.

Indexed as

Leukemia, Myeloid, AcuteProteogenomicsAdultChildDisease ProgressionHumansProteomicsRecurrence

Identifiers

PMID36572751
PMCPMC9991901
OpenAlexW4312211043

What OpenQuestion 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 OpenQuestion graph.