Evidence map›Paper›PMID 28668095›Full record

ReviewJournal of translational medicine2017

CSPG4: a prototype oncoantigen for translational immunotherapy studies.

Valeria Rolih, Giuseppina Barutello, Selina Iussich, Raffaella De Maria, Elena Quaglino, Paolo Buracco, Federica Cavallo, Federica Riccardo

Open access · goldAbstract readReview
In one paragraph

Review in Journal of translational medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

54 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. B7-H3 and CSPG4-targeted CAR T cells as potent effectors in anaplastic thyroid cancer.Journal of experimental & clinical cancer research : CR · 2025
    Article
  6. Review
  7. Article
  8. Human immuno-therapeutics for cancer treatment of dogs?Frontiers in veterinary science · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Chondroitin sulfate proteoglycan 4: An attractive target for antibody-based immunotherapy.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2024
    Review
  18. Article
  19. Review
  20. Article
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 at 1 institution in 1 country.

Valeria RolihDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, 10126, Turin, Italy.
Giuseppina BarutelloDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, 10126, Turin, Italy.
Selina IussichDepartment of Veterinary Sciences, University of Torino, 10095, Grugliasco, Italy.
Raffaella De MariaDepartment of Veterinary Sciences, University of Torino, 10095, Grugliasco, Italy.
Elena QuaglinoDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, 10126, Turin, Italy.
Paolo BuraccoDepartment of Veterinary Sciences, University of Torino, 10095, Grugliasco, Italy.
Federica CavalloDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, 10126, Turin, Italy.
Federica RiccardoDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, 10126, Turin, Italy. federica.riccardo@unito.it.ORCID 0000-0002-9692-0172
University of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thanks to striking progress in both the understanding of anti-tumor immune response and the characterization of several tumor associated antigens (TAA), a more rational design and more sophisticated strategies for anti-tumor vaccination have been possible. However, the effectiveness of cancer vaccines in clinical trial is still partial, indicating that additional studies are needed to optimize their design and their pre-clinical testing. Indeed, anti-tumor vaccination success relies on the choice of the best TAA to be targeted and on the translational power of the pre-clinical model used to assess its efficacy. The chondroitin sulfate proteoglycan-4 (CSPG4) is a cell surface proteoglycan overexpressed in a huge range of human and canine neoplastic lesions by tumor cells, tumor microenvironment and cancer initiating cells. CSPG4 plays a central role in the oncogenic pathways required for malignant progression and metastatization. Thanks to these features and to its poor expression in adult healthy tissues, CSPG4 represents an ideal oncoantigen and thus an attractive target for anti-tumor immunotherapy. In this review we explore the potential of CSPG4 immune-targeting. Moreover, since it has been clearly demonstrated that spontaneous canine tumors mimic the progression of human malignancies better than any other pre-clinical model available so far, we reported also our results indicating that CSPG4 DNA vaccination is safe and effective in significantly increasing the survival of canine melanoma patients. Therefore, anti-CSPG4 vaccination strategy could have a substantial impact for the treatment of the wider population of spontaneous CSPG4-positive tumor affected dogs with a priceless translational value and a revolutionary implication for human oncological patients.

Indexed as

ImmunotherapyTranslational Research, BiomedicalAnimalsAntigensAntigens, NeoplasmChondroitin Sulfate Proteoglycan 4HumansNeoplasmsProteoglycansVaccinationAntigensAntigens, NeoplasmChondroitin Sulfate Proteoglycan 4ProteoglycansCancer immunotherapyChondroitin sulfate proteoglycan-4 (CSPG4)Comparative oncologyDNA vaccination

Identifiers

PMID28668095
PMCPMC5494135
OpenAlexW2732743010

What OpenQuestion holds

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LicenceCC BY
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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.