Evidence map›Paper›PMID 18583325›Full record

ArticleThe American journal of pathology2008

MicroRNA-mediated down-regulation of PRDM1/Blimp-1 in Hodgkin/Reed-Sternberg cells: a potential pathogenetic lesion in Hodgkin lymphomas.

Kui Nie, Mario Gomez, Pablo Landgraf, Jose-Francisco Garcia, Yifang Liu, Leonard H C Tan, Amy Chadburn, Thomas Tuschl, Daniel M Knowles, Wayne Tam

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
6.0field-weighted citation impact, top 4% 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

85 citing papers in PubMed, 153 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Frontiers in cell and developmental biology · 2023
    Review
  5. Article
  6. Article
  7. Review
  8. MicroRNA signature in classical Hodgkin lymphoma.Journal of applied genetics · 2021
    Review
  9. Review
  10. Article
  11. Review
  12. Epigenetics of the antibody and autoantibody response.Current opinion in immunology · 2020
    Review
  13. Multifaceted Role of PRDM Proteins in Human Cancer.International journal of molecular sciences · 2020
    Review
  14. Myeloid leukemia with high EVI1 expression is sensitive to 5-aza-2'-deoxycytidine by targeting miR-9.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

25 more citing papers are in PubMed but not listed here.

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

10 authors at 5 institutions in 3 countries.

Kui NieDepartment of Pathology and Laboratory Medicine, Joan and Sanford I. Weill Medical College of Cornell University, New York, New York 10021, USA.
Mario Gomez
Pablo Landgraf
Jose-Francisco Garcia
Yifang Liu
Leonard H C Tan
Amy Chadburn
Thomas Tuschl
Daniel M Knowles
Wayne Tam
Howard Hughes Medical Institute · USCornell University · USRockefeller University · USSingapore General Hospital · SGSpanish National Cancer Research Centre · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PRDM1/Blimp-1, a master regulator in terminal B-cell differentiation, has been recently identified as a tumor suppressor target for mutational inactivation in diffuse large B-cell lymphomas of the activated B-cell type. Our studies here demonstrate that PRDM1/blimp-1 is also a target for microRNA (miRNA)-mediated down-regulation by miR-9 and let-7a in Hodgkin/Reed-Sternberg (HRS) cells of Hodgkin lymphoma (HL). MiRNA expression profiling by direct miRNA cloning demonstrated that both of these miRNAs are among the most highly expressed in cultured HRS cells. These miRNAs functionally targeted specific binding sites in the 3' untranslated region of PRDM1/blimp-1 mRNA and repressed luciferase reporter activities through repression of translation. In addition, high levels of miR-9 and let-7a in HL cell lines correlated with low levels of PRDM1/Blimp-1. Similar to their in vitro counterparts, the majority of HRS cells in primary HL cases showed weak or no PRDM1/Blimp-1 expression. Over-expression of miR-9 or let-7a reduced PRDM1/Blimp-1 levels in U266 cells by 30% to 50%, whereas simultaneous inhibition of their activities in L428 cells resulted in an approximately 2.6-fold induction in PRDM1/Blimp-1. MiRNA-mediated down-regulation of PRDM1/Blimp-1 may contribute to the phenotype maintenance and pathogenesis of HRS cells by interfering with normal B-cell terminal differentiation, thus representing a novel molecular lesion, as well as a potential therapeutic target in HL.

Indexed as

Gene Expression Regulation, Neoplastic3' Untranslated RegionsBlotting, WesternCell Line, TumorDown-RegulationEpigenesis, GeneticGene ExpressionGene Expression ProfilingHodgkin DiseaseHumansImmunohistochemistryMicroRNAsPositive Regulatory Domain I-Binding Factor 1Protein BiosynthesisReed-Sternberg CellsRepressor Proteins3' Untranslated RegionsMicroRNAsmirnlet7 microRNA, humanPositive Regulatory Domain I-Binding Factor 1PRDM1 protein, humanRepressor Proteins

Identifiers

PMID18583325
PMCPMC2438301
OpenAlexW2140017455

What OpenQuestion holds

Textmetadata
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.