Evidence map›Paper›PMID 27566657›Full record

ArticleCancer genomics & proteomics

Elevated O-GlcNAcylation of Extracellular Vesicle Proteins Derived from Metastatic Colorectal Cancer Cells.

Parunya Chaiyawat, Churat Weeraphan, Pukkavadee Netsirisawan, Daranee Chokchaichamnankit, Chantragan Srisomsap, Jisnuson Svasti, Voraratt Champattanachai

Abstract read
In one paragraph

Article in Cancer genomics & proteomics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
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  6. Cells · 2023
    Review
  7. Biomolecules · 2022
    Article
  8. Article
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  14. Article
  15. O-GlcNAc in cancer: An Oncometabolism-fueled vicious cycle.Journal of bioenergetics and biomembranes · 2018
    Review
  16. 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 1 country.

Parunya ChaiyawatApplied Biological Sciences Program, Chulabhorn Graduate Institute, Bangkok, Thailand.
Churat WeeraphanLaboratory of Biochemistry, Chulabhorn Research Institute, Bangkok, Thailand.
Pukkavadee NetsirisawanLaboratory of Biochemistry, Chulabhorn Research Institute, Bangkok, Thailand.
Daranee ChokchaichamnankitLaboratory of Biochemistry, Chulabhorn Research Institute, Bangkok, Thailand.
Chantragan SrisomsapApplied Biological Sciences Program, Chulabhorn Graduate Institute, Bangkok, Thailand Laboratory of Biochemistry, Chulabhorn Research Institute, Bangkok, Thailand.
Jisnuson SvastiApplied Biological Sciences Program, Chulabhorn Graduate Institute, Bangkok, Thailand Laboratory of Biochemistry, Chulabhorn Research Institute, Bangkok, Thailand.
Voraratt ChampattanachaiApplied Biological Sciences Program, Chulabhorn Graduate Institute, Bangkok, Thailand Laboratory of Biochemistry, Chulabhorn Research Institute, Bangkok, Thailand voraratt@cri.or.th.
Chulabhorn Research Institute · THChulabhorn Graduate Institute · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundO-GlcNAcylation is a single sugar attachment of serine and/or threonine residues on intracellular proteins. Recent reports reveal that it can modify several secretory proteins; however, the underlying mechanisms are largely unexplored. MATERIALS AND

methodsTo investigate whether extracellular vesicles (EVs) carry secretory O-GlcNAc-modified proteins that were isolated from colorectal cancer (CRC) cells, two-dimensional gel electrophoresis followed with O-GlcNAc immunoblotting and liquid chromatography-tandem mass spectrometry (LC-MS/MS) were applied.

resultsIt was revealed that the O-GlcNAc modification of many EV proteins was increased in metastatic cells. Among these, transitional endoplasmic reticulum ATPase (TER ATPase) and RuVB-like1 were successfully confirmed for the O-GlcNAc modification in which the levels were significantly higher in EVs of metastatic CRC cell line.

conclusionThese data, demonstrate that proteins carried by EVs are O-GlcNAc-modified. Importantly, elevated aberrant O-GlcNAcylation of EV proteins might serve as a potential biomarker of metastatic CRC.

Indexed as

Cell Line, TumorChromatography, LiquidColorectal NeoplasmsExtracellular VesiclesGlycoproteinsGlycosylationHumansNeoplasm MetastasisProteomicsReproducibility of ResultsTandem Mass SpectrometryGlycoproteinsColorectal cancerextracellular vesiclesmetastasisO-GlcNAcylationRuVB-like1transitional endoplasmic reticulum ATPase

Identifiers

PMID27566657
PMCPMC5070628
OpenAlexW2511047166

What OpenQuestion holds

Textmetadata
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.