Evidence map›Paper›PMID 25829250›Full record

ReviewBiochimica et biophysica acta2015

Insights into the key roles of proteoglycans in breast cancer biology and translational medicine.

Achilleas D Theocharis, Spyros S Skandalis, Thomas Neill, Hinke A B Multhaupt, Mario Hubo, Helena Frey, Sandeep Gopal, Angélica Gomes, Nikos Afratis, Hooi Ching Lim and 6 more

Open access · greenAbstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
8.3field-weighted citation impact, top 2% 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

80 citing papers in PubMed, 151 citations in OpenAlex.

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  12. Delineating highly transcribed noncoding elements landscape in breast cancer.Computational and structural biotechnology journal · 2023
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20 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

16 authors at 6 institutions in 5 countries.

Achilleas D TheocharisBiochemistry, Biochemical Analysis & Matrix Pathobiology Research Group, Laboratory of Biochemistry, Department of Chemistry, University of Patras, 26500 Patras, Greece.
Spyros S SkandalisBiochemistry, Biochemical Analysis & Matrix Pathobiology Research Group, Laboratory of Biochemistry, Department of Chemistry, University of Patras, 26500 Patras, Greece.
Thomas NeillDepartment of Pathology, Anatomy and Cell Biology and the Cancer Cell Biology and Signaling Program, Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Hinke A B MulthauptDepartment of Biomedical Sciences and Biotech Research & Innovation Center, University of Copenhagen, Denmark.
Mario HuboUniversity of Frankfurt, Institute of Pharmacology and Toxicology, Theodor-Stern Kai 7, Frankfurt 60590, Germany.
Helena FreyUniversity of Frankfurt, Institute of Pharmacology and Toxicology, Theodor-Stern Kai 7, Frankfurt 60590, Germany.
Sandeep GopalDepartment of Biomedical Sciences and Biotech Research & Innovation Center, University of Copenhagen, Denmark.
Angélica GomesDepartment of Biomedical Sciences and Biotech Research & Innovation Center, University of Copenhagen, Denmark.
Nikos AfratisDepartment of Biomedical Sciences and Biotech Research & Innovation Center, University of Copenhagen, Denmark.
Hooi Ching LimDepartment of Biomedical Sciences and Biotech Research & Innovation Center, University of Copenhagen, Denmark.
John R CouchmanDepartment of Biomedical Sciences and Biotech Research & Innovation Center, University of Copenhagen, Denmark.
Jorge FilmusDepartment of Biological Sciences, Sunnybrook Research Institute and Department of Medical Biophysics, University of Toronto, Canada.
Ralph D SandersonUniversity of Alabama at Birmingham, Department of Pathology, UAB Comprehensive Cancer Center, 1720 2nd Ave. S, WTI 602B, Birmingham, AL 35294, USA.
Liliana SchaeferUniversity of Frankfurt, Institute of Pharmacology and Toxicology, Theodor-Stern Kai 7, Frankfurt 60590, Germany.
Renato V IozzoDepartment of Pathology, Anatomy and Cell Biology and the Cancer Cell Biology and Signaling Program, Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Nikos K KaramanosBiochemistry, Biochemical Analysis & Matrix Pathobiology Research Group, Laboratory of Biochemistry, Department of Chemistry, University of Patras, 26500 Patras, Greece. Electronic address: n.k.karamanos@upatras.gr.
University of Copenhagen · DKGoethe University Frankfurt · DEUniversity of Patras · GRSidney Kimmel Cancer Center · USSunnybrook Health Science Centre · CAUniversity of Alabama at Birmingham · US

Funding

X-Ray Crystallography and Macromolecular CharacterizationP30CA056036 · NCI · THOMAS JEFFERSON UNIVERSITY · PI Andrew Chapman · 1995 to 2026
$94.8M
NEOPLASTIC MODULATION OF PROTEOGLYCAN METABOLISMR01CA039481 · NCI · UNIVERSITY OF PENNSYLVANIA · PI IOZZO, RENATO V. · 1985 to 2020
$7.1M
The Biology of Perlecan in Cancer and AngiogenesisR01CA047282 · NCI · THOMAS JEFFERSON UNIVERSITY · PI IOZZO, RENATO V. · 1990 to 2019
$5.7M
Heparanase Regulation of Myeloma Metastasis: Mechanism and TherapyR01CA138340 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SANDERSON, RALPH D · 2009 to 2018
$3.3M
Novel Heparanase Inhibitors for Cancer TherapyR01CA138535 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SANDERSON, RALPH D · 2010 to 2014
$1.8M
Progranulin signaling in bladder cancerR01CA164462 · NCI · THOMAS JEFFERSON UNIVERSITY · PI IOZZO, RENATO V., MORRIONE, ANDREA · 2012 to 2016
$1.6M
Natural EGFR Antagonists and CancerR01CA120975 · NCI · THOMAS JEFFERSON UNIVERSITY · PI IOZZO, RENATO V. · 2007 to 2010
$942k
NCI NIH HHS P30 CA056036NCI NIH HHS R01 CA039481NCI NIH HHS R01 CA047282NCI NIH HHS R01 CA120975NCI NIH HHS R01 CA138340NCI NIH HHS R01 CA 138535NCI NIH HHS R01 CA138535NCI NIH HHS R01 CA164462NCI NIH HHS R01 CA38340NCI NIH HHS R01 CA39481NCI NIH HHS R01 CA47282
6 · The paper itself

Abstract

Proteoglycans control numerous normal and pathological processes, among which are morphogenesis, tissue repair, inflammation, vascularization and cancer metastasis. During tumor development and growth, proteoglycan expression is markedly modified in the tumor microenvironment. Altered expression of proteoglycans on tumor and stromal cell membranes affects cancer cell signaling, growth and survival, cell adhesion, migration and angiogenesis. Despite the high complexity and heterogeneity of breast cancer, the rapid evolution in our knowledge that proteoglycans are among the key players in the breast tumor microenvironment suggests their potential as pharmacological targets in this type of cancer. It has been recently suggested that pharmacological treatment may target proteoglycan metabolism, their utilization as targets for immunotherapy or their direct use as therapeutic agents. The diversity inherent in the proteoglycans that will be presented herein provides the potential for multiple layers of regulation of breast tumor behavior. This review summarizes recent developments concerning the biology of selected proteoglycans in breast cancer, and presents potential targeted therapeutic approaches based on their novel key roles in breast cancer.

Indexed as

Translational Research, BiomedicalBreast NeoplasmsFemaleGene Expression Regulation, NeoplasticHumansMolecular Targeted TherapyNeovascularization, PathologicProteoglycansSignal TransductionTumor MicroenvironmentProteoglycansBreast cancerDecorinGlypicansProteoglycansSerglycinSyndecans

Identifiers

PMID25829250
PMCPMC4433619
OpenAlexW2020040573

What OpenQuestion holds

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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.