Evidence map›Paper›PMID 25140302›Full record

ReviewBioMed research international2014

The motile breast cancer phenotype roles of proteoglycans/glycosaminoglycans.

Dragana Nikitovic, Katerina Kouvidi, Kallirroi Voudouri, Aikaterini Berdiaki, Evgenia Karousou, Alberto Passi, George N Tzanakakis

Open access · hybridAbstract readReview
In one paragraph

Review in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Frontiers in cellular and infection microbiology · 2018
    Article
  11. Human Metaplastic Breast Carcinoma and Decorin.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2017
    Article
  12. Article
  13. Identification of a five-lncRNA signature for the diagnosis and prognosis of gastric cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. 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

7 authors at 2 institutions in 2 countries.

Dragana NikitovicLaboratory of Anatomy-Histology-Embryology, Medical School, University of Crete, 71003 Heraklion, Greece.
Katerina KouvidiLaboratory of Anatomy-Histology-Embryology, Medical School, University of Crete, 71003 Heraklion, Greece.
Kallirroi VoudouriLaboratory of Anatomy-Histology-Embryology, Medical School, University of Crete, 71003 Heraklion, Greece.
Aikaterini BerdiakiLaboratory of Anatomy-Histology-Embryology, Medical School, University of Crete, 71003 Heraklion, Greece.
Evgenia KarousouDipartimento di Scienze Chirurgiche e Morfologiche, Università degli Studi dell'Insubria, Via J.H. Dunant 5, 21100 Varese, Italy.
Alberto PassiDipartimento di Scienze Chirurgiche e Morfologiche, Università degli Studi dell'Insubria, Via J.H. Dunant 5, 21100 Varese, Italy.
George N TzanakakisLaboratory of Anatomy-Histology-Embryology, Medical School, University of Crete, 71003 Heraklion, Greece.
University of Crete · GRUniversity of Insubria · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The consecutive stages of cancer growth and dissemination are obligatorily perpetrated through specific interactions of the tumor cells with their microenvironment. Importantly, cell-associated and tumor microenvironment glycosaminoglycans (GAGs)/proteoglycan (PG) content and distribution are markedly altered during tumor pathogenesis and progression. GAGs and PGs perform multiple functions in specific stages of the metastatic cascade due to their defined structure and ability to interact with both ligands and receptors regulating cancer pathogenesis. Thus, GAGs/PGs may modulate downstream signaling of key cellular mediators including insulin growth factor receptor (IGFR), epidermal growth factor receptor (EGFR), estrogen receptors (ERs), or Wnt members. In the present review we will focus on breast cancer motility in correlation with their GAG/PG content and critically discuss mechanisms involved. Furthermore, new approaches involving GAGs/PGs as potential prognostic/diagnostic markers or as therapeutic agents for cancer-related pathologies are being proposed.

Indexed as

Biomarkers, TumorBreast NeoplasmsCarcinogenesisCell MovementFemaleGene Expression Regulation, NeoplasticHumansNeoplasm ProteinsProteoglycansSignal TransductionTumor MicroenvironmentBiomarkers, TumorNeoplasm ProteinsProteoglycans

Identifiers

PMID25140302
PMCPMC4129668
OpenAlexW2109380508

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.