Evidence map›Paper›PMID 42074135›Full record

ArticleInternational journal of molecular sciences2026

GD2 Identifies Cancer Stemness in Glioblastoma and Phytoalexin Library Screen Identifies Potential Novel Natural Inhibitors.

Khoa Nguyen, Emily McConnell, Minh Tran, Nathan Burow, Orielle Edwards, Thomas Cheng, Jane E Cavanaugh, Patrick T Flaherty, Reza Izadpanah, Bridgette M Collins-Burow and 2 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Khoa NguyenDepartment of Medicine, Section of Hematology and Oncology, Tulane University School of Medicine, Tulane Cancer Center, New Orleans, LA 70112, USA.ORCID 0000-0002-8059-6136
Emily McConnellDepartment of Medicine, Section of Hematology and Oncology, Tulane University School of Medicine, Tulane Cancer Center, New Orleans, LA 70112, USA.
Minh TranDepartment of Medicine, Section of Hematology and Oncology, Tulane University School of Medicine, Tulane Cancer Center, New Orleans, LA 70112, USA.ORCID 0009-0009-2935-9918
Nathan BurowDepartment of Medicine, Section of Hematology and Oncology, Tulane University School of Medicine, Tulane Cancer Center, New Orleans, LA 70112, USA.
Orielle EdwardsDepartment of Medicine, Section of Hematology and Oncology, Tulane University School of Medicine, Tulane Cancer Center, New Orleans, LA 70112, USA.
Thomas ChengDepartment of Medicine, Section of Hematology and Oncology, Tulane University School of Medicine, Tulane Cancer Center, New Orleans, LA 70112, USA.
Jane E CavanaughDepartment of Pharmacological Sciences, Division of Medicinal Chemistry, Mylan School of Pharmacy, Duquesne University, Pittsburgh, PA 15218, USA.
Patrick T FlahertyDepartment of Pharmacological Sciences, Division of Medicinal Chemistry, Mylan School of Pharmacy, Duquesne University, Pittsburgh, PA 15218, USA.
Reza IzadpanahDepartment of Surgery, Tulane University Health Science Center, New Orleans, LA 70112, USA.
Bridgette M Collins-BurowDepartment of Medicine, Section of Hematology and Oncology, Tulane University School of Medicine, Tulane Cancer Center, New Orleans, LA 70112, USA.
Stephen BoueU.S. Department of Agriculture, Agricultural Research Service, Southern Regional Research Center, New Orleans, LA 70179, USA.ORCID 0000-0002-2790-4427
Matthew E BurowDepartment of Medicine, Section of Hematology and Oncology, Tulane University School of Medicine, Tulane Cancer Center, New Orleans, LA 70112, USA.ORCID 0000-0002-0642-6630

Funding

USDA USDA
6 · The paper itself

Abstract

Glioblastoma (GBM) is the most aggressive and prevalent primary brain tumor in adults, characterized by rapid growth, diffuse infiltration, and a dismal prognosis. Despite advances in conventional therapies, the median survival remains approximately one year, emphasizing the urgent need for novel therapeutic strategies. GD2, a disialoganglioside overexpressed in several malignancies, has been implicated in tumorigenesis and metastasis and has been identified as a cancer stem cell marker. While previous reports have identified high levels of GD2 expression in gliomas compared to normal brain tissue, its role in GBM stemness remains controversial. In this study, we revisited prior findings refuting GD2's involvement in GBM stemness by replicating key tumorigenesis experiments and further explored its impact on stemness properties such as migration and metabolic plasticity. Additionally, a phytochemical screen was used to identify natural compounds as potential inhibitors targeting GD2-mediated tumorigenesis. Our findings aim to clarify GD2's role in GBM and provide insights into novel therapeutic interventions.

Indexed as

Brain NeoplasmsGangliosidesGlioblastomaNeoplastic Stem CellsSesquiterpenesAnimalsCell Line, TumorCell MovementHumansPhytoalexinsGangliosidesPhytoalexinsSesquiterpenescancer stem cellsGD2glioblastoma multiformephytochemicals

Identifiers

PMID42074135
PMCPMC13115847

What OpenQuestion 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 OpenQuestion graph.