Evidence map›Paper›PMID 39993803›Full record

ArticleCancer genomics & proteomics

Correlation of GD2 Biosynthesis Enzymes With Cancer Stem Cell Markers in Human Breast Cancer.

Niamh S O'Neill, Mariam Rizk, Amber X Li, Tracey A Martin, Wen G Jiang, Kefah Mokbel

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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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

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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

3 citing papers in PubMed.

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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

6 authors.

Niamh S O'NeillCCMR, Cardiff University School of Medicine, Heath Park, Cardiff, U.K.
Mariam RizkThe London Breast Institute, Princess Grace Hospital, London, U.K.
Amber X LiCCMR, Cardiff University School of Medicine, Heath Park, Cardiff, U.K.
Tracey A MartinCCMR, Cardiff University School of Medicine, Heath Park, Cardiff, U.K.
Wen G JiangCCMR, Cardiff University School of Medicine, Heath Park, Cardiff, U.K.
Kefah MokbelThe London Breast Institute, Princess Grace Hospital, London, U.K. Kefah.Mokbel@hcahealthcare.co.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimThe disialoganglioside GD2 has been shown to promote cell proliferation, migration, tumor and metastasis through specific signaling pathways in tumor cells originating from the neuroectoderm, including melanomas, neuroblastomas, glioblastomas, and breast carcinomas. GD2 has therefore emerged as a potential diagnostic biomarker in early malignancy as evidenced by the high specificity of its expression in tumor cells. Furthermore, recent findings show that GD2 might also act as a novel cancer stem cell (CSC) marker. Our study aimed to investigate the relationship between GD2 and 34 recognized CSC markers in human breast cancer. MATERIALS AND

methodsWe analyzed the relationship between the mRNA expression profiles of three key enzymes involved in the biosynthesis of GD2 - B4GalT5, B4GALNT1, and ST8SIA1 - and 34 CSC markers in 91 human breast cancer tissue samples.

resultsAll three enzymes had positive and statistically significant correlation between each other with

conclusionThese findings lend further support to the growing evidence that GD2 is a potential biomarker of CSCs and epithelial-mesenchymal transition (EMT) in human breast cancer that can be amenable to therapeutic targeting.

Indexed as

Biomarkers, TumorBreast NeoplasmsGangliosidesN-AcetylgalactosaminyltransferasesNeoplastic Stem CellsSialyltransferasesFemaleHumansMiddle Agedalpha-N-acetylneuraminate alpha-2,8-sialyltransferaseBiomarkers, Tumorganglioside, GD2GangliosidesN-AcetylgalactosaminyltransferasesSialyltransferasesbreast cancercancer stem cellsEMTepithelial-mesenchymal transitiongangliosidesGD2GD3

Identifiers

PMID39993803
PMCPMC11880921

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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.