Evidence map›Paper›PMID 39921214›Full record

ReviewCancer science2025

GD2 is a Crucial Ganglioside in the Signal Modulation and Application as a Target of Cancer Therapeutics.

Koichi Furukawa, Yuhsuke Ohmi, Kazunori Hamamura, Yuki Ohkawa, Noboru Hashimoto, Orie Tajima, Kei Kaneko, Keiko Furukawa

Abstract readReview
In one paragraph

Review in Cancer science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Decoding the Role of Lipid Metabolism and Membrane Dynamics in Melanoma.International journal of molecular sciences · 2026
    Review
  6. Review
  7. 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

8 authors.

Koichi FurukawaDepartment of Biomedical Sciences, Chubu University College of Life and Health Sciences, Matsumoto, Kasugai, Japan.ORCID https://orcid.org/0000-0002-3321-9784
Yuhsuke OhmiDepartment of Clinical Engineering, Chubu University College of Life and Health Sciences, Matsumoto, Kasugai, Japan.
Kazunori HamamuraDepartment of Pharmacology, Aichi Gakuin University School of Dentistry, Nagoya, Japan.
Yuki OhkawaDepartment of GlycoOncology, Osaka International Cancer Center Institute, Osaka, Japan.
Noboru HashimotoDepartment of Tissue Regeneration, Tokushima University Graduate School of Biomedical Science, Tokushima, Japan.
Orie TajimaDepartment of Biomedical Sciences, Chubu University College of Life and Health Sciences, Matsumoto, Kasugai, Japan.
Kei KanekoDepartment of Biomedical Sciences, Chubu University College of Life and Health Sciences, Matsumoto, Kasugai, Japan.
Keiko FurukawaDepartment of Biomedical Sciences, Chubu University College of Life and Health Sciences, Matsumoto, Kasugai, Japan.

Funding

the Ministry of Education, Culture, Sports, Science and Technology of Japan 19K07393the Ministry of Education, Culture, Sports, Science and Technology of Japan 19K22518the Ministry of Education, Culture, Sports, Science and Technology of Japan 21K26828the Ministry of Education, Culture, Sports, Science and Technology of Japan JPMJCR17H2
6 · The paper itself

Abstract

While various glycosphingolipids were identified as cancer-associated carbohydrate antigens to be used as tumor markers, disialylated gangliosides such as GD3 and GD2 have particularly attracted attention from many researchers as promising cancer-associated antigens. Simultaneously, their functions in cancer and normal tissues have also been reported. Although GD3 is expressed at the early neural developmental stage and in various cancers, it is also found in the activated status of some normal cells such as astrocytes and lymphocytes. On the other hand, GD2 is expressed in more restricted cells than GD3, enabling anti-GD2 immune therapy to be more applicable for immunotherapy. Recently, the expression of GD2 has been reported in various epithelial cancers and neuroectoderm-derived tumors. The involvement of GD2 in cancer stem cell propertiesand the roles of GD2 in the signal modulation to bring about cancer stemness are now some of the most fascinating research topics. Cancer immunotherapy targeting GD2 by anti-GD2 antibody or anti-GD2 CAR-T is now widely being challenged with various modifications such as combination with cytokines, chemotherapy, or immune checkpoint blocking.

Indexed as

GangliosidesNeoplasmsAnimalsHumansImmunotherapyNeoplastic Stem CellsSignal Transductionganglioside, GD2Gangliosidescancer antigengangliosideimmunotherapylipid raftssignal

Identifiers

PMID39921214
PMCPMC11967270

What OpenQuestion holds

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Registered trials

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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.