Evidence map›Paper›PMID 31791414›Full record

ArticleClinical epigenetics2019

DNA methylation profiles in chronic lymphocytic leukemia patients treated with chemoimmunotherapy.

Maria Tsagiopoulou, Nikos Papakonstantinou, Theodoros Moysiadis, Larry Mansouri, Viktor Ljungström, Martí Duran-Ferrer, Andigoni Malousi, Ana C Queirós, Karla Plevova, Sujata Bhoi and 12 more

Open access · goldAbstract read
In one paragraph

Article in Clinical epigenetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

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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

22 authors at 13 institutions in 7 countries.

Maria TsagiopoulouInstitute of Applied Biosciences, Center for Research and Technology Hellas, 6th km Charilaou-Thermi Rd, 57001, Thermi, Thessaloniki, GR, Greece.
Nikos PapakonstantinouInstitute of Applied Biosciences, Center for Research and Technology Hellas, 6th km Charilaou-Thermi Rd, 57001, Thermi, Thessaloniki, GR, Greece.
Theodoros MoysiadisInstitute of Applied Biosciences, Center for Research and Technology Hellas, 6th km Charilaou-Thermi Rd, 57001, Thermi, Thessaloniki, GR, Greece.
Larry MansouriDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Viktor LjungströmDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Martí Duran-FerrerInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Departamento de Fundamentos Clínicos, Universitat de Barcelona, Barcelona, Spain.
Andigoni MalousiLaboratory of Biological Chemistry, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Ana C QueirósInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Departamento de Fundamentos Clínicos, Universitat de Barcelona, Barcelona, Spain.
Karla PlevovaDepartment of Internal Medicine-Hematology and Oncology, University Hospital Brno and Medical Faculty of Masaryk University, Brno, Czech Republic.
Sujata BhoiDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Panagoula KolliaDepartment of Biology, National and Kapodistrian University of Athens, Athens, Greece.
David OscierDepartment of Haematology, Royal Bournemouth Hospital, Bournemouth, UK.
Achilles AnagnostopoulosHematology Department and HCT Unit, G. Papanicolaou Hospital, Thessaloniki, Greece.
Livio TrentinDepartment of Medicine, Hematology and Clinical Immunology Branch, Padua University School of Medicine, Padua, Italy.
Matthias RitgenSecond Medical Department, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Sarka PospisilovaDepartment of Internal Medicine-Hematology and Oncology, University Hospital Brno and Medical Faculty of Masaryk University, Brno, Czech Republic.
Niki StavroyianniHematology Department and HCT Unit, G. Papanicolaou Hospital, Thessaloniki, Greece.
Paolo GhiaDivision of Experimental Oncology and Department of Onco-Hematology, IRCCS San Raffaele Scientific Institute and Università Vita-Salute San Raffaele, Milan, Italy.
Jose I Martin-SuberoInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Departamento de Fundamentos Clínicos, Universitat de Barcelona, Barcelona, Spain.
Christiane PottSecond Medical Department, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Richard RosenquistDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Kostas StamatopoulosInstitute of Applied Biosciences, Center for Research and Technology Hellas, 6th km Charilaou-Thermi Rd, 57001, Thermi, Thessaloniki, GR, Greece. kostas.stamatopoulos@gmail.com.ORCID 0000-0001-8529-640X
Karolinska Institutet · SEUppsala University · SECentral European Institute of Technology · CZConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESG. Papanikolaou General Hospital · GRNational and Kapodistrian University of Athens · GRUniversity Hospital Schleswig-Holstein · DEAristotle University of Thessaloniki · GRCentre for Research and Technology Hellas · GRInstitució Catalana de Recerca i Estudis Avançats · ESRoyal Bournemouth Hospital · GBUniversity of Padua · ITVita-Salute San Raffaele University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn order to gain insight into the contribution of DNA methylation to disease progression of chronic lymphocytic leukemia (CLL), using 450K Illumina arrays, we determined the DNA methylation profiles in paired pre-treatment/relapse samples from 34 CLL patients treated with chemoimmunotherapy, mostly (n = 31) with the fludarabine-cyclophosphamide-rituximab (FCR) regimen.

resultsThe extent of identified changes in CLL cells versus memory B cells from healthy donors was termed "epigenetic burden" (EB) whereas the number of changes between the pre-treatment versus the relapse sample was termed "relapse changes" (RC). Significant (p < 0.05) associations were identified between (i) high EB and short time-to-first-treatment (TTFT); and, (ii) few RCs and short time-to-relapse. Both the EB and the RC clustered in specific genomic regions and chromatin states, including regulatory regions containing binding sites of transcription factors implicated in B cell and CLL biology.

conclusionsOverall, we show that DNA methylation in CLL follows different dynamics in response to chemoimmunotherapy. These epigenetic alterations were linked with specific clinical and biological features.

Indexed as

AdultAgedCyclophosphamideDisease ProgressionDNA MethylationEpigenesis, GeneticFemaleGene Regulatory NetworksHigh-Throughput Nucleotide SequencingHumansImmunotherapyLeukemia, Lymphocytic, Chronic, B-CellLongitudinal StudiesMaleMiddle AgedOligonucleotide Array Sequence AnalysisCyclophosphamidefludarabineRituximabVidarabineChemoimmunotherapyCLLDNA methylationMicroarray analysisRelapse

Identifiers

PMID31791414
PMCPMC6889736
OpenAlexW2993102490

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Registered trials

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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.