Evidence map›Paper›PMID 33205006›Full record

ArticleFASEB bioAdvances2020

Gb3-cSrc complex in glycosphingolipid-enriched microdomains contributes to the expression of p53 mutant protein and cancer drug resistance via β-catenin-activated RNA methylation.

Kartik R Roy, Mohammad B Uddin, Sagor C Roy, Ronald A Hill, John Marshall, Yu-Teh Li, Jean Christopher Chamcheu, Hua Lu, Yong-Yu Liu

Open access · goldAbstract read
In one paragraph

Article in FASEB bioAdvances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  5. Review
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  11. Role of Globotriaosylceramide in Physiology and Pathology.Frontiers in molecular biosciences · 2022
    Review
  12. Article
  13. The mMolecular cancer · 2021
    Review
  14. 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.

Kartik R RoySchool of Basic Pharmaceutical and Toxicological Sciences College of Pharmacy University of Louisiana at Monroe Monroe Louisiana USA.
Mohammad B UddinSchool of Basic Pharmaceutical and Toxicological Sciences College of Pharmacy University of Louisiana at Monroe Monroe Louisiana USA.
Sagor C RoySchool of Basic Pharmaceutical and Toxicological Sciences College of Pharmacy University of Louisiana at Monroe Monroe Louisiana USA.
Ronald A HillSchool of Basic Pharmaceutical and Toxicological Sciences College of Pharmacy University of Louisiana at Monroe Monroe Louisiana USA.
John MarshallDepartment of Rare Genetic Disease Research Sanofi-Genzyme R&D Center Genzyme, Framingham Massachusetts USA.
Yu-Teh LiDepartment of Biochemistry and Molecular Biology Tulane University School of Medicine New Orleans Louisiana USA.
Jean Christopher ChamcheuSchool of Basic Pharmaceutical and Toxicological Sciences College of Pharmacy University of Louisiana at Monroe Monroe Louisiana USA.
Hua LuDepartment of Biochemistry and Molecular Biology Tulane University School of Medicine New Orleans Louisiana USA.
Yong-Yu LiuSchool of Basic Pharmaceutical and Toxicological Sciences College of Pharmacy University of Louisiana at Monroe Monroe Louisiana USA.
University of Louisiana at Monroe · USTulane University · USGenesys (United States) · US

Funding

STABILITY' (symptomatic review during biologic therapy) Review in Inflammatory Bowel DiseaseP20GM103424 · NIGMS · LOUISIANA STATE UNIV A&M COL BATON ROUGE · PI Seetharama D Jois · 2012 to 2026
$57.4M
Ceramide glycosylation determines the stemness of cancer stem cellsR15CA167476 · NCI · UNIVERSITY OF LOUISIANA AT MONROE · PI LIU, YONG-YU · 2013 to 2013
$413k
NCI NIH HHS R15 CA167476NIGMS NIH HHS P20 GM103424
6 · The paper itself

Abstract

Glucosylceramide synthase (GCS) is a key enzyme catalyzing ceramide glycosylation to generate glucosylceramide (GlcCer), which in turn serves as the precursor for cells to produce glycosphingolipids (GSLs). In cell membranes, GSLs serve as essential components of GSL-enriched microdomains (GEMs) and mediate membrane functions and cell behaviors. Previous studies showed that ceramide glycosylation correlates with upregulated expression of p53 hotspot mutant R273H and cancer drug resistance. Yet, the underlying mechanisms remain elusive. We report herewith that globotriaosylceramide (Gb3) is associated with cSrc kinase in GEMs and plays a crucial role in modulating expression of p53 R273H mutant and drug resistance. Colon cancer cell lines, either WiDr homozygous for missense-mutated

Indexed as

colon cancercSrc kinasedrug resistanceglycosphingolipid‐enriched microdomainsglycosphingolipidsmissense mutationp53 tumor suppressor

Identifiers

PMID33205006
PMCPMC7655095
OpenAlexW3048687648

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.