Evidence map›Paper›PMID 31988291›Full record

ArticleScientific reports2020

B4GALNT1 induces angiogenesis, anchorage independence growth and motility, and promotes tumorigenesis in melanoma by induction of ganglioside GM2/GD2.

Hideki Yoshida, Lisa Koodie, Kari Jacobsen, Ken Hanzawa, Yasuhide Miyamoto, Masato Yamamoto

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 45 citations in OpenAlex.

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  8. GD2-targeted theranostics of neuroblastoma with [European journal of nuclear medicine and molecular imaging · 2025
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  10. Glycosylation in Cancer.Handbook of experimental pharmacology · 2025
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  12. Article
  13. Review
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  15. Downregulation ofZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2024
    Article
  16. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Hideki YoshidaDepartment of Surgery, University of Minnesota, Minneapolis, Minnesota, USA.
Lisa KoodieDepartment of Surgery, University of Minnesota, Minneapolis, Minnesota, USA.
Kari JacobsenDepartment of Surgery, University of Minnesota, Minneapolis, Minnesota, USA.
Ken HanzawaDepartment of Molecular Biology, Osaka International Cancer Institute, Osaka, Japan.
Yasuhide MiyamotoDepartment of Molecular Biology, Osaka International Cancer Institute, Osaka, Japan.
Masato YamamotoDepartment of Surgery, University of Minnesota, Minneapolis, Minnesota, USA. yamam016@umn.edu.
University of Minnesota · USOsaka Medical Center for Cancer and Cardiovascular Diseases · JPUniversity of Minnesota Medical Center · US

Funding

Combination therapy with IFN expressing oncolytic adenovirus for pancreatic cancerR01CA228760 · NCI · UNIVERSITY OF MINNESOTA · PI DAVYDOVA, JULIA, YAMAMOTO, MASATO · 2019 to 2023
$1.7M
Systemic Therapy with Infectivity-Selective Oncolytic Adenovirus for PDACR01CA196215 · NCI · UNIVERSITY OF MINNESOTA · PI YAMAMOTO, MASATO · 2016 to 2020
$1.7M
Next Generation Oncolytic Adenovirus for Advanced Pancreatic Cancer TreatmentR01CA168448 · NCI · UNIVERSITY OF MINNESOTA · PI YAMAMOTO, MASATO · 2013 to 2017
$1.6M
NCI NIH HHS R01 CA168448NCI NIH HHS R01 CA196215NCI NIH HHS R01 CA228760
6 · The paper itself

Abstract

β-1,4-N-Acetyl-Galactosaminyltransferase 1 (B4GALNT1) encodes the key enzyme B4GALNT1 to generate gangliosides GM2/GD2. GM2/GD2 gangliosides are surface glycolipids mainly found on brain neurons as well as peripheral nerves and skin melanocytes and are reported to exacerbate the malignant potential of melanomas. In order to elucidate the mechanism, we performed functional analyses of B4GALNT1-overexpressing cells. We analyzed ganglioside pattern on four melanoma and two neuroblastoma cell lines by high performance liquid chromatography (HPLC). We overexpressed B4GALNT1 in GM2/GD2-negative human melanoma cell line (SH4) and confirmed production of GM2/GD2 by HPLC. They showed higher anchorage independence growth (AIG) in colony formation assay, and exhibited augmented motility. In vitro, cell proliferation was not affected by GM2/GD2 expression. In vivo, GM2/GD2-positive SH4 clones showed significantly higher tumorigenesis in NOD/Scid/IL2Rγ-null mice, and immunostaining of mouse CD31 revealed that GM2/GD2 induced remarkable angiogenesis. No differences were seen in melanoma stem cell and Epithelial-Mesenchymal Transition markers between GM2/GD2-positive and -negative SH4 cells. We therefore concluded that B4GALNT1, and consequently GM2/GD2, enhanced tumorigenesis via induction of angiogenesis, AIG, and cell motility. RNA-Seq suggested periostin as a potential key factor for angiogenesis and AIG. These findings may lead to development of novel therapy for refractory melanoma.

Indexed as

AnimalsCarcinogenesisCell Line, TumorCell MovementCell ProliferationFemaleG(M2) GangliosideHeterograftsHumansMaleMelanomaMiceMice, Inbred NODMice, SCIDN-AcetylgalactosaminyltransferasesNeovascularization, PathologicB4galnt1 protein, humanG(M2) GangliosideN-Acetylgalactosaminyltransferases

Identifiers

PMID31988291
PMCPMC6985110
OpenAlexW3001348553

What OpenQuestion holds

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LicenceCC BY
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.