Evidence map›Paper›PMID 31671543›Full record

ArticleCancers2019

Fibroblasts in Nodular Sclerosing Classical Hodgkin Lymphoma Are Defined by a Specific Phenotype and Protect Tumor Cells from Brentuximab-Vedotin Induced Injury.

Katrin Bankov, Claudia Döring, Adam Ustaszewski, Maciej Giefing, Marco Herling, Chiara Cencioni, Francesco Spallotta, Carlo Gaetano, Ralf Küppers, Martin-Leo Hansmann and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Spatial transcriptomics reveals prognostically LYZCancer immunology, immunotherapy : CII · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Detecting Fibroblast Activation Proteins in Lymphoma UsingJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2022
    Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. 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

11 authors at 7 institutions in 3 countries.

Katrin BankovDr. Senckenberg Institute of Pathology, Goethe University, 60590 Frankfurt am Main, Germany. katrin.bankov@kgu.de.
Claudia DöringDr. Senckenberg Institute of Pathology, Goethe University, 60590 Frankfurt am Main, Germany. c.doering@em.uni-frankfurt.de.
Adam UstaszewskiInstitute of Human Genetics, Polish Academy of Sciences, 60-479 Poznan, Poland. adam.ustaszewski@igcz.poznan.pl.
Maciej GiefingInstitute of Human Genetics, Polish Academy of Sciences, 60-479 Poznan, Poland. giefingm@man.poznan.pl.ORCID 0000-0002-4760-8246
Marco HerlingThe Laboratory of Lymphocyte Signalling and Oncoproteome, Department I of Internal Medicine, Center for Integrated Oncology (CIO) Aachen-Bonn-Cologne-Duesseldorf, CECAD and CMMC, University of Cologne, 50937 Cologne, Germany. marco.herling@uk-koeln.de.
Chiara CencioniNational Research Council (CNR), Institute for Systems Analysis and Computer Science, 00185 Rome, Italy. chcencioni@gmail.com.
Francesco SpallottaDepartment of Oncology, University of Turin, 10060 Candiolo (Turin), Italy. fspallotta@gmail.com.
Carlo GaetanoLaboratorio di Epigenetica, Istituti Clinici Scientifici Maugeri IRCCS, 27100 Pavia, Italy. carlo.gaetano@icsmaugeri.it.
Ralf KüppersInstitute of Cell Biology (Cancer Research), University of Duisburg-Essen, 45122 Essen, Germany. ralf.kueppers@uk-essen.de.ORCID 0000-0002-6691-7191
Martin-Leo HansmannDr. Senckenberg Institute of Pathology, Goethe University, 60590 Frankfurt am Main, Germany. martin-leo.hansmann@kgu.de.
Sylvia HartmannDr. Senckenberg Institute of Pathology, Goethe University, 60590 Frankfurt am Main, Germany. s.hartmann@em.uni-frankfurt.de.ORCID 0000-0003-3424-1091
Goethe University Frankfurt · DEInstitute of Human Genetics · PLCandiolo Cancer Institute · ITIstituti Clinici Scientifici Maugeri · ITNational Research Council · ITUniversity of Cologne · DEUniversity of Duisburg-Essen · DE

Funding

Deutsche Forschungsgemeinschaft HA6145/2-1, HE 3552/4-2, HA 1284/7-2, KU1315/9-2
6 · The paper itself

Abstract

Classical Hodgkin lymphoma (cHL) is one of the most common malignant lymphomas in Western Europe. The nodular sclerosing subtype of cHL (NS cHL) is characterized by a proliferation of fibroblasts in the tumor microenvironment, leading to fibrotic bands surrounding the lymphoma infiltrate. Several studies have described a crosstalk between the tumour cells of cHL, the Hodgkin- and Reed-Sternberg (HRS) cells, and cancer-associated fibroblasts. However, to date a deep molecular characterization of these fibroblasts is lacking. Thus, the aim of the present study is a comprehensive characterization of these fibroblasts. Gene expression profiling and methylation profiles of fibroblasts isolated from primary lymph node suspensions revealed persistent differences between fibroblasts obtained from NS cHL and lymphadenitis. NS cHL derived fibroblasts exhibit a myofibroblastic phenotype characterized by myocardin (

Indexed as

classical Hodgkin lymphomafibroblastsgene expression analysisluteolinmethylation profilingnodular sclerosis

Identifiers

PMID31671543
PMCPMC6896072
OpenAlexW2982569245

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.