Evidence map›Paper›PMID 29743654›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2018

Expression of the transcription factor ZBTB46 distinguishes human histiocytic disorders of classical dendritic cell origin.

Ansuman T Satpathy, Ryanne A Brown, Ellen Gomulia, Carlos G Briseño, Maxwell R Mumbach, Zenggang Pan, Kenneth M Murphy, Yasodha Natkunam, Howard Y Chang, Jinah Kim

Open access · bronzeAbstract read
In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Rosai-Dorfman disease.Pathologica · 2021
    Review
  7. Article
  8. 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

10 authors at 4 institutions in 1 country.

Ansuman T SatpathyDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, 94305, USA. satpathy@stanford.edu.ORCID http://orcid.org/0000-0002-5167-537X
Ryanne A BrownDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Ellen GomuliaDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Carlos G BriseñoDepartment of Pathology and Immunology and Howard Hughes Medical Institute, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Maxwell R MumbachCenter for Personal Dynamic Regulomes, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Zenggang PanDepartment of Pathology, University of Colorado Denver, Aurora, CO, 80045, USA.
Kenneth M MurphyDepartment of Pathology and Immunology and Howard Hughes Medical Institute, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Yasodha NatkunamDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Howard Y ChangCenter for Personal Dynamic Regulomes, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Jinah KimDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Stanford University · USHoward Hughes Medical Institute · USStanford Medicine · USUniversity of Colorado Denver · US

Funding

NHLBI NIH HHS L30 HL134161
6 · The paper itself

Abstract

Distinguishing classical dendritic cells from other myeloid cell types is complicated by the shared expression of cell surface markers. ZBTB46 is a zinc finger and BTB domain-containing transcription factor, which is expressed by dendritic cells and committed dendritic cell precursors, but not by plasmacytoid dendritic cells, monocytes, macrophages, or other immune cell populations. In this study, we demonstrate that expression of ZBTB46 identifies human dendritic cell neoplasms. We examined ZBTB46 expression in a range of benign and malignant histiocytic disorders and found that ZBTB46 is able to clearly define the dendritic cell identity of many previously unclassified histiocytic disease subtypes. In particular, all examined cases of Langerhans cell histiocytosis and histiocytic sarcoma expressed ZBTB46, while all cases of blastic plasmacytoid dendritic cell neoplasm, chronic myelomonocytic leukemia, juvenile xanthogranuloma, Rosai-Dorfman disease, and Erdheim-Chester disease failed to demonstrate expression of ZBTB46. Moreover, ZBTB46 expression clarified the identity of diagnostically challenging neoplasms, such as cases of indeterminate cell histiocytosis, classifying a fraction of these entities as dendritic cell malignancies. These findings clarify the lineage origins of human histiocytic disorders and distinguish dendritic cell disorders from all other myeloid neoplasms.

Indexed as

AdolescentAdultAgedChildChild, PreschoolDendritic CellsDiagnosis, DifferentialFemaleHistiocytosisHumansInfantInfant, NewbornMaleMiddle AgedMyeloid CellsTranscription FactorsTranscription FactorsZbtb46 protein, human

Identifiers

PMID29743654
PMCPMC6138663
OpenAlexW2801645040

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.