Evidence map›Paper›PMID 28864076›Full record

ArticleThe Journal of investigative dermatology2018

The Role of Fibroblast Growth Factor-Binding Protein 1 in Skin Carcinogenesis and Inflammation.

Marcel Oliver Schmidt, Khalid Ammar Garman, Yong Gu Lee, Chong Zuo, Patrick James Beck, Mingjun Tan, Juan Antonio Aguilar-Pimentel, Markus Ollert, Carsten Schmidt-Weber, Helmut Fuchs and 6 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

31 citing papers in PubMed, 40 citations in OpenAlex.

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  8. Decoding the Function ofAnimals : an open access journal from MDPI · 2025
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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

16 authors at 3 institutions in 4 countries.

Marcel Oliver SchmidtLombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA. Electronic address: mos6@georgetown.edu.
Khalid Ammar GarmanLombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
Yong Gu LeeLombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA; Department of Chemistry, Purdue University System, West Lafayette, Indiana, USA.
Chong ZuoLombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA; Department of Medicine, Washington University in Saint Louis School of Medicine, Saint Louis, Missouri, USA.
Patrick James BeckLombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA; Department of Chemistry, Thomas Jefferson High School for Science and Technology, Alexandria, Virginia, USA.
Mingjun TanLombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
Juan Antonio Aguilar-PimentelGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Markus OllertDepartment of Infection and Immunity, Luxembourg Institute of Health, Esch-sur-Alzette, Luxembourg; Department of Dermatology and Allergy Center, Odense Research Center for Anaphylaxis, University of Southern Denmark, Odense, Denmark.
Carsten Schmidt-WeberCenter of Allergy & Environment (ZAUM), Technische Universität München (TUM) and Helmholtz Zentrum, Munich, Germany; German Center for Lung Research (DZL), Gießen, Germany.
Helmut FuchsGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Valerie Gailus-DurnerGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Martin Hrabe de AngelisGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany; Chair of Experimental Genetics, Center of Life and Food Sciences Weihenstephan, Technische Universität München, München, Germany; German Center for Diabetes Research (DZD), Neuherberg, Germany.
German Mouse Clinic Consortium
Elena TassiLombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
Anna Tate RiegelLombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
Anton WellsteinLombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA. Electronic address: anton.wellstein@georgetown.edu.
Georgetown University · USHelmholtz Zentrum München · DEUniversity of Southern Denmark · DK

Funding

Tissue Culture Shared ResourceP30CA051008 · NCI · GEORGETOWN UNIVERSITY · PI STEPHEN W BYERS · 1990 to 2026
$71.5M
Renal Vascular Oxidative Stress in HypertensionP01HL068686 · NHLBI · GEORGETOWN UNIVERSITY · PI JOSE, PEDRO A., SANDBERG, KATHRYN L · 2001 to 2017
$28.8M
BIOLOGY AND PATHOLOGY OF A MODULATOR OF FGFR01CA071508 · NCI · GEORGETOWN UNIVERSITY · PI WELLSTEIN, ANTON · 1997 to 2010
$2.9M
Advancing Child Health: Preparing the Next Generation of Pediatric Researchers.R25HD082842 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI KRANTZ, IAN D. · 2015 to 2019
$540k
NCI NIH HHS P30 CA051008NCI NIH HHS R01 CA071508NHLBI NIH HHS P01 HL068686NICHD NIH HHS R25 HD082842
6 · The paper itself

Abstract

Fibroblast growth factor-binding protein 1 (FGFBP1) is a secreted chaperone that mobilizes paracrine-acting FGFs, stored in the extracellular matrix, and presents them to their cognate receptors. FGFBP1 enhances FGF signaling including angiogenesis during cancer progression and is upregulated in various cancers. Here we evaluated the contribution of endogenous FGFBP1 to a wide range of organ functions as well as to skin pathologies using Fgfbp1-knockout mice. Relative to wild-type littermates, knockout mice showed no gross pathologies. Still, in knockout mice a significant thickening of the epidermis associated with a decreased transepidermal water loss and increased proinflammatory gene expression in the skin was detected. Also, skin carcinogen challenge by 7,12-dimethylbenz[a]anthracene/12-O-tetradecanoyl-phorbol-13-acetate resulted in delayed and reduced papillomatosis in knockout mice. This was paralleled by delayed healing of skin wounds and reduced angiogenic sprouting in subcutaneous matrigel plugs. Heterozygous green fluorescent protein (GFP)-knock-in mice revealed rapid induction of gene expression during papilloma induction and during wound healing. Examination of wild-type skin grafted onto Fgfbp1 GFP-knock-in reporter hosts and bone marrow transplants from the GFP-reporter model into wild-type hosts revealed that circulating Fgfbp1-expressing cells migrate into healing wounds. We conclude that tissue-resident and circulating Fgfbp1-expressing cells modulate skin carcinogenesis and inflammation.

Indexed as

AnimalsBone MarrowBone Marrow TransplantationCarcinogenesisCarcinogensCarrier ProteinsFemaleHumansInflammationIntercellular Signaling Peptides and ProteinsIntracellular Signaling Peptides and ProteinsMaleMiceMice, Inbred C57BLMice, KnockoutNeoplasms, ExperimentalCarcinogensCarrier ProteinsFgfbp1 protein, mouseIntercellular Signaling Peptides and ProteinsIntracellular Signaling Peptides and ProteinsTetradecanoylphorbol Acetate

Identifiers

PMID28864076
PMCPMC5742071
OpenAlexW2751737963

What OpenQuestion holds

Textmetadata
LicenceTDM
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.