Evidence map›Paper›PMID 31200555›Full record

ArticleCancers2019

Dissecting the Prognostic Significance and Functional Role of Progranulin in Chronic Lymphocytic Leukemia.

Lena Schulze-Edinghausen, Claudia Dürr, Selcen Öztürk, Manuela Zucknick, Axel Benner, Verena Kalter, Sibylle Ohl, Viola Close, Patrick Wuchter, Stephan Stilgenbauer and 2 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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Drug Discovery from Gene Expression/Gene Regulation.Methods in molecular biology (Clifton, N.J.) · 2026
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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 4 institutions in 2 countries.

Lena Schulze-EdinghausenDivision of Molecular Genetics, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany. l.schulze-edinghausen@dkfz-heidelberg.de.
Claudia DürrDivision of Molecular Genetics, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany. claudi.duerr@gmail.com.
Selcen ÖztürkDivision of Molecular Genetics, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany. s.oeztuerk@dkfz-heidelberg.de.
Manuela ZucknickOslo Centre for Biostatistics and Epidemiology, Department of Biostatistics, Institute of Basic Medical Sciences, Faculty of Medicine, University of Oslo, 0372 Oslo, Norway. manuela.zucknick@medisin.uio.no.
Axel BennerDivision of Biostatistics, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany. benner@dkfz-heidelberg.de.
Verena KalterDivision of Molecular Genetics, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany. v.kalter@dkfz-heidelberg.de.
Sibylle OhlDivision of Molecular Genetics, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany. s.ohl@dkfz-heidelberg.de.
Viola CloseInternal Medicine III, University of Ulm, 89081 Ulm, Germany, and Cooperation Unit Mechanisms of Leukemogenesis, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany. viola.close@outlook.com.
Patrick WuchterInstitute of Transfusion Medicine and Immunology, Medical Faculty Mannheim, Heidelberg University, German Red Cross Blood Service Baden-Württemberg-Hessen, 68167 Mannheim, Germany. patrick.wuchter@medma.uni-heidelberg.de.
Stephan StilgenbauerInternal Medicine III, University of Ulm, 89081 Ulm, Germany, and Department of Internal Medicine I, Saarland University, 66421 Homburg, Germany. stephan.stilgenbauer@uniklinik-ulm.de.
Peter LichterDivision of Molecular Genetics, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany. peter.lichter@dkfz-heidelberg.de.
Martina SeiffertDivision of Molecular Genetics, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany. m.seiffert@dkfz-heidelberg.de.
German Cancer Research Center · DEHeidelberg University · DEUniversität Ulm · DEUniversity of Oslo · NO

Funding

Bundesministerium für Bildung und Forschung BMBF-Network "PRECiSe" (031L0076A)Bundesministerium für Bildung und Forschung ERA-NET TRANSCAN-2 program JTC 2014-project FIRE-CLLDeutsche Forschungsgemeinschaft SFB1074 project B1Helmholtz Virtuelles Institut Undertanding and overcoming resistance to apoptosis and therapy in leukemia
6 · The paper itself

Abstract

Chronic lymphocytic leukemia (CLL) is known for its strong dependency on the tumor microenvironment. We found progranulin (GRN), a protein that has been linked to inflammation and cancer, to be upregulated in the serum of CLL patients compared to healthy controls, and increased GRN levels to be associated with an increased hazard for disease progression and death. This raised the question of whether GRN is a functional driver of CLL. We observed that recombinant GRN did not directly affect viability, activation, or proliferation of primary CLL cells in vitro. However, GRN secretion was induced in co-cultures of CLL cells with stromal cells that enhanced CLL cell survival. Gene expression profiling and protein analyses revealed that primary mesenchymal stromal cells (MSCs) in co-culture with CLL cells acquire a cancer-associated fibroblast-like phenotype. Despite its upregulation in the co-cultures, GRN treatment of MSCs did not mimic this effect. To test the relevance of GRN for

Indexed as

cancer-associated fibroblastschronic lymphocytic leukemiaprognostic serum markerprogranulintumor microenvironment

Identifiers

PMID31200555
PMCPMC6627891
OpenAlexW2949749766

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.