Evidence map›Paper›PMID 30027065›Full record

ReviewAnalytical cellular pathology (Amsterdam)2018

Heparan Sulfate Proteoglycans in Human Colorectal Cancer.

Carolina Meloni Vicente, Daiana Aparecida da Silva, Priscila Veronica Sartorio, Tiago Donizetti Silva, Sarhan Sydney Saad, Helena Bonciani Nader, Nora Manoukian Forones, Leny Toma

Open access · goldAbstract readReview
In one paragraph

Review in Analytical cellular pathology (Amsterdam), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 11% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Carolina Meloni VicenteDisciplina de Biologia Molecular, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Três de Maio, 100 4° Andar, Vila Clementino, São Paulo, SP, Brazil.ORCID 0000-0001-8584-2845
Daiana Aparecida da SilvaDisciplina de Biologia Molecular, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Três de Maio, 100 4° Andar, Vila Clementino, São Paulo, SP, Brazil.
Priscila Veronica SartorioDisciplina de Farmacologia Celular, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Três de Maio, 100 4° Andar, Vila Clementino, São Paulo, SP, Brazil.
Tiago Donizetti SilvaDisciplina de Gastroenterologia Clínica, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Loefgreen 1726, Vila Clementino, São Paulo, SP, Brazil.
Sarhan Sydney SaadDisciplina de Gastroenterologia Cirúrgica, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Napoleão de Barros, 715 2° Andar, Vila Clementino, São Paulo, SP, Brazil.
Helena Bonciani NaderDisciplina de Biologia Molecular, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Três de Maio, 100 4° Andar, Vila Clementino, São Paulo, SP, Brazil.
Nora Manoukian ForonesDisciplina de Gastroenterologia Clínica, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Loefgreen 1726, Vila Clementino, São Paulo, SP, Brazil.
Leny TomaDisciplina de Biologia Molecular, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Três de Maio, 100 4° Andar, Vila Clementino, São Paulo, SP, Brazil.
Universidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer is the third most common cancer worldwide, accounting for more than 610,000 mortalities every year. Prognosis of patients is highly dependent on the disease stage at diagnosis. Therefore, it is crucial to investigate molecules involved in colorectal cancer tumorigenesis, with possible use as tumor markers. Heparan sulfate proteoglycans are complex molecules present in the cell membrane and extracellular matrix, which play vital roles in cell adhesion, migration, proliferation, and signaling pathways. In colorectal cancer, the cell surface proteoglycan syndecan-2 is upregulated and increases cell migration. Moreover, expression of syndecan-1 and syndecan-4, generally antitumor molecules, is reduced. Levels of glypicans and perlecan are also altered in colorectal cancer; however, their role in tumor progression is not fully understood. In addition, studies have reported increased heparan sulfate remodeling enzymes, as the endosulfatases. Therefore, heparan sulfate proteoglycans are candidate molecules to clarify colorectal cancer tumorigenesis, as well as important targets to therapy and diagnosis.

Indexed as

Colorectal NeoplasmsGlypicansHeparan Sulfate ProteoglycansHumansSyndecan-2Syndecan-4GlypicansHeparan Sulfate ProteoglycansperlecanSyndecan-2Syndecan-4

Identifiers

PMID30027065
PMCPMC6031075
OpenAlexW2809637071

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.