Evidence map›Paper›PMID 33660254›Full record

ReviewThe British journal of dermatology2021

Melanoma-associated glycosyltransferase GCNT2 as an emerging biomarker and therapeutic target.

M Perez, A Chakraborty, L S Lau, N B B Mohammed, C J Dimitroff

Open access · greenAbstract readReview
In one paragraph

Review in The British journal of dermatology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  8. Hypomethylation ofFrontiers in immunology · 2025
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  16. Aberrant Protein Glycosylation in Brain Cancers, with Emphasis on Glioblastoma.Advances in experimental medicine and biology · 2022
    Article
  17. 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 1 institution in 1 country.

M PerezDepartment of Translational Medicine, Translational Glycobiology Institute at FIU, Herbert Wertheim College of Medicine, Florida International University, Miami, FL, USA.
A ChakrabortyDepartment of Translational Medicine, Translational Glycobiology Institute at FIU, Herbert Wertheim College of Medicine, Florida International University, Miami, FL, USA.
L S LauDepartment of Translational Medicine, Translational Glycobiology Institute at FIU, Herbert Wertheim College of Medicine, Florida International University, Miami, FL, USA.
N B B MohammedDepartment of Translational Medicine, Translational Glycobiology Institute at FIU, Herbert Wertheim College of Medicine, Florida International University, Miami, FL, USA.
C J DimitroffDepartment of Translational Medicine, Translational Glycobiology Institute at FIU, Herbert Wertheim College of Medicine, Florida International University, Miami, FL, USA.ORCID 0000-0002-4224-7621
Florida International University · US

Funding

Analysis of Glycomic Regulators in Melanoma ProgressionU01CA225644 · NCI · FLORIDA INTERNATIONAL UNIVERSITY · PI DIMITROFF, CHARLES J · 2019 to 2023
$2.4M
Analysis of vascular Galectin-9 as an immunomodulator of B-cell activityR21AI146368 · NIAID · FLORIDA INTERNATIONAL UNIVERSITY · PI DIMITROFF, CHARLES J · 2019 to 2020
$384k
NCI NIH HHS U01 CA225644NIAID NIH HHS R21 AI146368
6 · The paper itself

Abstract

In metastatic melanoma, with a dismal survival rate and propensity for treatment resistance and recurrence, it is critical to establish biomarkers that better predict treatment response and disease severity. The melanoma glycome, composed of complex carbohydrates termed glycans, is an under-investigated area of research, although it is gaining momentum in the cancer biomarker and therapeutics field. Novel findings suggest that glycans play a major role in influencing melanoma progression and could be exploited for prognosticating metastatic activity and/or as therapeutic targets. In this review, we discuss the role of aberrant glycosylation, particularly the specialized function of β1,6 N-acetylglucosaminyltransferase 2 (GCNT2), in melanoma pathogenesis and summarize mechanisms of GCNT2 regulation to illuminate its potential as a predictive marker and therapeutic target.

Indexed as

GlycosyltransferasesMelanomaBiomarkersCell Line, TumorHumansN-AcetylglucosaminyltransferasesN-AcetylhexosaminyltransferasesNeoplasm Recurrence, LocalBiomarkersGCNT2 protein, humanGlycosyltransferasesN-AcetylglucosaminyltransferasesN-Acetylhexosaminyltransferases

Identifiers

PMID33660254
PMCPMC8373636
OpenAlexW3134035358

What OpenQuestion holds

Textmetadata
LicenceTDM
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.