Evidence map›Paper›PMID 25677902›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2015

miR expression in MYC-negative DLBCL/BL with partial trisomy 11 is similar to classical Burkitt lymphoma and different from diffuse large B-cell lymphoma.

Michalina Zajdel, Grzegorz Rymkiewicz, Magdalena Chechlinska, Katarzyna Blachnio, Barbara Pienkowska-Grela, Beata Grygalewicz, Krzysztof Goryca, Maria Cieslikowska, Zbigniew Bystydzienski, Pawel Swoboda and 2 more

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Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. microRNA Profile of High-Grade B-Cell Lymphoma with 11q Aberration.International journal of molecular sciences · 2024
    Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. A comprehensive flow-cytometry-based immunophenotypic characterization of Burkitt-like lymphoma with 11q aberration.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2018
    Article
  10. Current understanding of the role and regulation of miRNAs in Burkitt lymphoma.Blood and lymphatic cancer : targets and therapy · 2018
    Review
  11. Review
  12. Article
  13. miR-155 as a Biomarker in B-Cell Malignancies.BioMed research international · 2016
    Review
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

12 authors at 1 institution in 1 country.

Michalina ZajdelDepartment of Immunology, Maria Sklodowska-Curie Memorial Centre and Institute of Oncology, Roentgen 5, 02-781, Warsaw, Poland.
Grzegorz Rymkiewicz
Magdalena Chechlinska
Katarzyna Blachnio
Barbara Pienkowska-Grela
Beata Grygalewicz
Krzysztof Goryca
Maria Cieslikowska
Zbigniew Bystydzienski
Pawel Swoboda
Jan Walewski
Jan Konrad Siwicki
The Maria Sklodowska-Curie National Research Institute of Oncology · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fast and reliable differential diagnosis of Burkitt lymphoma (BL) vs. diffuse large B cell lymphoma (DLBCL) is of major importance for therapeutic decisions and patient outcome. Aggressive B cell non-Hodgkin lymphomas (B-NHLs) that do not belong to the abovementioned entities were categorized by the current WHO lymphoma classification as "B-cell lymphoma, unclassifiable, with features intermediate between DLBCL and BL" (DLBCL/BL). We have recently described a DLBCL/BL subgroup with recurrent chromosome 11q aberrations, resembling BL (B-NHLs[11q]). Here, we analyzed 102 prospectively collected fine needle aspirates from patients with aggressive B-NHLs in order to investigate the potential of microRNA (miR)-155, its precursor BIC, as well as miR-21 and miR-26a to differentiate BL from DLBCL, and from DLBCL/BL that include B-NHLs[11q]. Both BL and DLBCL/BL cases, including B-NHLs[11q], demonstrated significantly lower expression levels of miR-155/BIC, miR-21, and miR-26a compared to primary DLBCL. In conclusion, the miRs expression in B-NHLs[11q] provides a new suggestion, in addition to pathomorphological and clinical similarities between classical, i.e., MYC translocation-positive BL, and B-NHLs[11q], to recognize the B-NHLs[11q] subgroup of DLBCL/BL category as a MYC translocation-negative variant of BL in most cases, and points to the potential utility of miR-155/BIC/miR-21/miR-26a for the differential diagnosis of a heterogeneous category of DLBCL/BL.

Indexed as

Diagnosis, DifferentialAdolescentAdultAgedAged, 80 and overBiopsy, Fine-NeedleBurkitt LymphomaChromosomes, Human, Pair 11FemaleGene Expression Regulation, NeoplasticHumansImmunophenotypingIn Situ Hybridization, FluorescenceLymphoma, Large B-Cell, DiffuseMaleMicroRNAsMicroRNAsMYC protein, humanProto-Oncogene Proteins c-myc

Identifiers

PMID25677902
OpenAlexW1986501925

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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.