Evidence map›Paper›PMID 36669592›Full record

ArticleMolecular & cellular proteomics : MCP2023

O-Glycomic and Proteomic Signatures of Spontaneous and Butyrate-Stimulated Colorectal Cancer Cell Line Differentiation.

K Madunić, Y M C A Luijkx, O A Mayboroda, G M C Janssen, P A van Veelen, K Strijbis, T Wennekes, G S M Lageveen-Kammeijer, M Wuhrer

Open access · goldAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Article
  6. ComprehensiveAnalytical chemistry · 2024
    Article
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

9 authors at 3 institutions in 1 country.

K MadunićCenter for Proteomics and Metabolomics, Leiden University, The Netherlands.
Y M C A LuijkxDepartment Chemical Biology and Drug Discovery, Utrecht Institute for Pharmaceutical Sciences and Bijvoet Center for Biomolecular Research, Utrecht University, Utrecht, The Netherlands; Department Biomolecular Health Sciences, Utrecht University, Utrecht, The Netherlands.
O A MayborodaCenter for Proteomics and Metabolomics, Leiden University, The Netherlands.
G M C JanssenCenter for Proteomics and Metabolomics, Leiden University, The Netherlands.
P A van VeelenCenter for Proteomics and Metabolomics, Leiden University, The Netherlands.
K StrijbisDepartment Biomolecular Health Sciences, Utrecht University, Utrecht, The Netherlands.
T WennekesDepartment Chemical Biology and Drug Discovery, Utrecht Institute for Pharmaceutical Sciences and Bijvoet Center for Biomolecular Research, Utrecht University, Utrecht, The Netherlands.
G S M Lageveen-KammeijerCenter for Proteomics and Metabolomics, Leiden University, The Netherlands.
M WuhrerCenter for Proteomics and Metabolomics, Leiden University, The Netherlands. Electronic address: m.wuhrer@lumc.nl.
Leiden University · NLUtrecht University · NLUniversity of Applied Sciences Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gut microbiota of the gastrointestinal tract provide health benefits to the human host via bacterial metabolites. Bacterial butyrate has beneficial effects on intestinal homeostasis and is the preferred energy source of intestinal epithelial cells, capable of inducing differentiation. It was previously observed that changes in the expression of specific proteins as well as protein glycosylation occur with differentiation. In this study, specific mucin O-glycans were identified that mark butyrate-induced epithelial differentiation of the intestinal cell line CaCo-2 (Cancer Coli-2), by applying porous graphitized carbon nano-liquid chromatography with electrospray ionization tandem mass spectrometry. Moreover, a quantitative proteomic approach was used to decipher changes in the cell proteome. It was found that the fully differentiated butyrate-stimulated cells are characterized by a higher expression of sialylated O-glycan structures, whereas fucosylation is downregulated with differentiation. By performing an integrative approach, we generated hypotheses about the origin of the observed O-glycome changes. These insights pave the way for future endeavors to study the dynamic O-glycosylation patterns in the gut, either produced via cellular biosynthesis or through the action of bacterial glycosidases as well as the functional role of these patterns in homeostasis and dysbiosis at the gut-microbiota interface.

Indexed as

Colorectal NeoplasmsProteomicsButyratesCaco-2 CellsCell DifferentiationGlycomicsHumansPolysaccharidesButyratesPolysaccharidesCaCo-2differentiationglycomicsomics integrationPGC-LC–MS/MSproteomics

Identifiers

PMID36669592
PMCPMC9999233
OpenAlexW4317233457

What Socratic holds

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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 Socratic graph.