Evidence map›Paper›PMID 33628777›Full record

ArticleBioMed research international2021

Peripheral Blood Cells from Patients with Hodgkin's and Diffuse Large B Cell Lymphomas May Be a Better Source of Candidate Diagnostic miRNAs Than Circulating miRNAs.

Ewa Paszkiewicz-Kozik, Agnieszka Paziewska, Maria Kulecka, Michalina Dąbrowska, Anna Kluska, Aneta Bałabas, Magdalena Piątkowska, Filip Ambrożkiewicz, Joanna Tajer, Włodzimierz Osiadacz and 9 more

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 99% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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 3 institutions in 2 countries.

Ewa Paszkiewicz-KozikDepartment of Lymphoproliferative Diseases, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw 02-781, Poland.ORCID https://orcid.org/0000-0003-2629-3932
Agnieszka PaziewskaDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781, Poland.ORCID https://orcid.org/0000-0002-6644-1509
Maria KuleckaDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781, Poland.ORCID https://orcid.org/0000-0002-9830-8892
Michalina DąbrowskaDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781, Poland.ORCID https://orcid.org/0000-0002-7585-4946
Anna KluskaDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781, Poland.ORCID https://orcid.org/0000-0002-5087-6575
Aneta BałabasDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781, Poland.ORCID https://orcid.org/0000-0003-0228-7650
Magdalena PiątkowskaDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781, Poland.ORCID https://orcid.org/0000-0001-8372-8002
Filip AmbrożkiewiczDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781, Poland.ORCID https://orcid.org/0000-0001-6850-780X
Joanna TajerDepartment of Lymphoproliferative Diseases, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw 02-781, Poland.ORCID https://orcid.org/0000-0002-8962-1887
Włodzimierz OsiadaczDepartment of Lymphoproliferative Diseases, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw 02-781, Poland.ORCID https://orcid.org/0000-0003-1064-4902
Joanna Romejko-JarosińskaDepartment of Lymphoproliferative Diseases, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw 02-781, Poland.ORCID https://orcid.org/0000-0003-4603-1112
Martyna KotarskaDepartment of Lymphoproliferative Diseases, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw 02-781, Poland.ORCID https://orcid.org/0000-0003-3918-9704
Natalia Żeber-LubeckaDepartment of Gastroenterology and Hepatology, Medical Center for Postgraduate Education, Warsaw 02-781, Poland.ORCID https://orcid.org/0000-0003-4036-3191
Jakub KarczmarskiDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781, Poland.ORCID https://orcid.org/0000-0002-7976-0365
Lidia PopławskaDepartment of Lymphoproliferative Diseases, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw 02-781, Poland.ORCID https://orcid.org/0000-0003-3496-6308
Michał MikulaDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781, Poland.ORCID https://orcid.org/0000-0003-3447-7328
Piotr RutkowskiDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw 02-781, Poland.ORCID https://orcid.org/0000-0002-8920-5429
Jan WalewskiDepartment of Lymphoproliferative Diseases, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw 02-781, Poland.ORCID https://orcid.org/0000-0003-4247-2674
Jerzy OstrowskiDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781, Poland.ORCID https://orcid.org/0000-0003-1363-3766
Maria Curie-Skłodowska University · PLNational Institute of Oncology · HUPostgraduate School of Molecular Medicine · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hodgkin lymphoma (HL) and diffuse large B cell lymphoma (DLBCL) represent 15% and 20%, respectively, of all lymphoma types. The aim of this study was to identify and compare circulating serum miRNA (c-miRNA) and peripheral whole blood miRNA (wb-miRNA) profiles in patients with these lymphomas. Serum samples (20 HL, 21 DLBCL, and 30 healthy controls) and whole blood samples (21 HL, 17 DLBCL patients, and 30 healthy controls) were collected at the time of diagnosis. Serum and whole blood were also collected from 18 HL/17 DLBCL and eight HL/nine DLBCL patients, respectively, after treatment. Pairwise comparisons identified 125 c-miRNAs (adjusted

Indexed as

Hodgkin DiseaseLymphoma, Large B-Cell, DiffuseMicroRNAsAdultAgedAged, 80 and overCirculating MicroRNACohort StudiesFemaleHumansLeukocytes, MononuclearMaleMiddle AgedTranscriptomeYoung AdultCirculating MicroRNAMicroRNAs

Identifiers

PMID33628777
PMCPMC7880712
OpenAlexW3127096396

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.