Evidence map›Paper›PMID 40614178›Full record

ArticleScience advances2025

Integrated in vivo functional screens and multiomics analyses identify α-2,3-sialylation as essential for melanoma maintenance.

Praveen Agrawal, Shuhui Chen, Ana de Pablos, Yellamandayya Vadlamudi, Fatemeh Vand-Rajabpour, Faezeh Jame-Chenarboo, Swarnali Kar, Amanda Flores Yanke, Pietro Berico, Eleazar Miera Saenz de Vega and 5 more

Abstract read
In one paragraph

Article in Science advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

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

9 citing papers in PubMed.

  1. α2,3-Sialyltransferase (ST3Gal1) regulates endometrioid-type epithelial ovarian cancer cell migration and invasion via VEGF-R2/JAK2/STAT3 signaling cascades.International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Praveen AgrawalDepartment of Pathology, NYU Grossman School of Medicine, New York, NY, USA.ORCID 0000-0002-8892-9169
Shuhui ChenDepartment of Chemistry, New York University, New York, NY, USA.
Ana de PablosDepartment of Pathology, NYU Grossman School of Medicine, New York, NY, USA.ORCID 0000-0001-9028-0576
Yellamandayya VadlamudiDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0000-0003-3053-7151
Fatemeh Vand-RajabpourDepartment of Pathology, NYU Grossman School of Medicine, New York, NY, USA.ORCID 0000-0002-5833-6071
Faezeh Jame-ChenarbooDepartment of Chemistry, University of Alberta, Edmonton, Canada.ORCID 0000-0002-3880-2549
Swarnali KarDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0009-0002-7979-8715
Amanda Flores YankeDepartment of Pathology, NYU Grossman School of Medicine, New York, NY, USA.
Pietro BericoDepartment of Pathology, NYU Grossman School of Medicine, New York, NY, USA.ORCID 0000-0001-8034-0790
Eleazar Miera Saenz de VegaDepartment of Dermatology, NYU Grossman School of Medicine, New York, NY, USA.ORCID 0000-0001-8443-1286
Farbod DarvishianDepartment of Pathology, NYU Grossman School of Medicine, New York, NY, USA.
Iman OsmanInterdisciplinary Melanoma Cooperative Group, Perlmutter Cancer Center, NYU Langone Health, New York, NY, USA.ORCID 0000-0002-1472-1971
Amaia LujambioIcahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID 0000-0002-2798-1481
Lara K MahalDepartment of Chemistry, New York University, New York, NY, USA.ORCID 0000-0003-4791-8524
Eva HernandoDepartment of Pathology, NYU Grossman School of Medicine, New York, NY, USA.ORCID 0000-0003-1023-0312

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI MARK Reid PHILIPS · 1985 to 2026
$83.1M
Project 3: The Evolving Role of Regional Lymph Nodes in Melanoma ProgressionU54CA263001 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Eva Hernando · 2022 to 2026
$11.6M
Post-translational control of cancer cell stress response and metastasisR01CA202027 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AIFANTIS, IANNIS, HERNANDO, EVA · 2016 to 2020
$2.3M
Glycosylation as a Regulator of Tropism of Melanoma Metastasis - Resubmission - 1K22CA229600 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI AGRAWAL, PRAVEEN · 2021 to 2023
$583k
NCI NIH HHS K22 CA229600NCI NIH HHS P30 CA016087NCI NIH HHS R01 CA202027NCI NIH HHS U54 CA263001
6 · The paper itself

Abstract

Aberrant glycosylation is a hallmark of cancer biology, and altered glycosylation influences multiple facets of melanoma progression. To identify glycosyltransferases, glycans, and glycoproteins essential for melanoma maintenance, we conducted an in vivo growth screen with a pooled short hairpin RNA library of glycosyltransferases, lectin microarray profiling of benign nevus and melanoma samples, and mass spectrometry-based glycoproteomics. We found that α-2,3-sialyltransferases ST3GAL1 and ST3GAL2 and corresponding α-2,3-linked sialosides are up-regulated in melanoma compared to nevi and are essential for melanoma growth. Glycoproteomics revealed that glycoprotein targets of ST3GAL1 and ST3GAL2 are enriched in transmembrane proteins involved in growth signaling, including the amino acid transporter SLC3A2/CD98hc. CD98hc suppression mimicked the effect of ST3GAL1 and ST3GAL2 silencing, inhibiting melanoma cell proliferation. We found that both CD98hc protein stability and its prosurvival effect on melanoma are dependent upon α-2,3-sialylation mediated by ST3GAL1 and ST3GAL2. Our studies reveal α-2,3-sialosides functionally contributing to melanoma maintenance, supporting ST3GAL1 and ST3GAL2 as therapeutic targets in melanoma.

Indexed as

MelanomaProteomicsSialyltransferasesAnimalsbeta-Galactoside alpha-2,3-SialyltransferaseCell Line, TumorCell ProliferationFusion Regulatory Protein 1, Heavy ChainGlycoproteinsGlycosylationHumansMiceMultiomicsbeta-Galactoside alpha-2,3-SialyltransferaseFusion Regulatory Protein 1, Heavy ChainGlycoproteinsSialyltransferasesST3GAL1 protein, human

Identifiers

PMID40614178
PMCPMC12227053

What Socratic holds

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LicenceCC BY-NC
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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.