Evidence map›Paper›PMID 35028012›Full record

ArticleOncotarget2022

Altered glycosylation of several metastasis-associated glycoproteins with terminal GalNAc defines the highly invasive cancer cell phenotype.

Elham Khosrowabadi, Tomasz Wenta, Salla Keskitalo, Aki Manninen, Sakari Kellokumpu

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 36 citations in OpenAlex.

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  12. Role of TruncatedCancers · 2023
    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

5 authors at 2 institutions in 1 country.

Elham KhosrowabadiUniversity of Oulu, Faculty of Biochemistry and Molecular Medicine, Oulu, Finland.
Tomasz WentaUniversity of Oulu, Faculty of Biochemistry and Molecular Medicine, Oulu, Finland.
Salla KeskitaloInstitute of Biotechnology, University of Helsinki, Helsinki, Finland.
Aki ManninenUniversity of Oulu, Faculty of Biochemistry and Molecular Medicine, Oulu, Finland.
Sakari KellokumpuUniversity of Oulu, Faculty of Biochemistry and Molecular Medicine, Oulu, Finland.
University of Oulu · FIUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several distinct metastasis-associated glycosylation changes have been shown to promote cancer cell invasion and metastasis, the main cause of death of cancer patients. However, it is unclear whether their presence reflects cell- or tissue-specific variations for metastasis, or species needed to drive different phases of the metastatic cascade. To address this issue from a different perspective, we investigated here whether different cancer cell lines share any glycotopes that are common and important for their invasive phenotype. By using lectin microarray glycan profiling and an established myoma tissue-based 3D invasion assay, we identified a single glycotope recognized by

Indexed as

Matrix Metalloproteinase 14NeoplasmsChromatography, LiquidErbB ReceptorsGlycoproteinsGlycosylationHumansIntegrin beta4LectinsPhenotypePolysaccharidesTandem Mass SpectrometryErbB ReceptorsGlycoproteinsIntegrin beta4LectinsMatrix Metalloproteinase 14PolysaccharidescancerglycocodeglycosylationHelix Pomatia agglutinin (HPA)invasionterminal GalNAc

Identifiers

PMID35028012
PMCPMC8751650
OpenAlexW4205250398

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.