Evidence map›Paper›PMID 37057287›Full record

ArticleJournal of Cancer2023

PReferentially Expressed Antigen in MElanoma (PRAME): preliminary communication on a translational tool able to early detect Oral Malignant Melanoma (OMM).

Eliano Cascardi, Gerardo Cazzato, Giuseppe Ingravallo, Miriam Dellino, Carmelo Lupo, Nadia Casatta, Andrea Ballini, Andrea Pacifici, Gaetano Marenzi, Gilberto Sammartino and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of Cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. PRAME Expression in Melanoma is Negatively Regulated by TET2-Mediated DNA Hydroxymethylation.Laboratory investigation; a journal of technical methods and pathology · 2025
    Article
  4. Article
  5. 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

12 authors at 5 institutions in 2 countries.

Eliano CascardiDepartment of Medical Sciences, University of Turin, 10124 Turin, Italy.
Gerardo CazzatoSection of Molecular Pathology Department of Precision and Regenerative Medicine and Ionian Area (DiMePRe-J), University of Bari "Aldo Moro", Bari, 70124, Italy.
Giuseppe IngravalloSection of Molecular Pathology Department of Precision and Regenerative Medicine and Ionian Area (DiMePRe-J), University of Bari "Aldo Moro", Bari, 70124, Italy.
Miriam DellinoDepartment of Biomedical Sciences and Human Oncology, University of Bari, 70121 Bari, Italy.
Carmelo LupoInnovation Department, Diapath S.p.A., Via Savoldini n.71, 24057 Martinengo, Italy.
Nadia CasattaInnovation Department, Diapath S.p.A., Via Savoldini n.71, 24057 Martinengo, Italy.
Andrea BalliniDepartment of Precision Medicine, University of Campania "Luigi Vanvitelli", 80138 Naples, Italy.
Andrea PacificiDepartment of Oral and Maxillo-Facial Sciences, Sapienza University of Rome, 00195 Rome, Italy.
Gaetano MarenziDepartment of Neurosciences, Reproductive and Odontostomatological Sciences, University "Federico II" of Naples, via S. Pansini 5, 80131 Naples, Italy.
Gilberto SammartinoDepartment of Neurosciences, Reproductive and Odontostomatological Sciences, University "Federico II" of Naples, via S. Pansini 5, 80131 Naples, Italy.
Eugenio MaioranoSection of Molecular Pathology Department of Precision and Regenerative Medicine and Ionian Area (DiMePRe-J), University of Bari "Aldo Moro", Bari, 70124, Italy.
Marco TatulloDepartment of Neurosciences, Reproductive and Odontostomatological Sciences, University "Federico II" of Naples, via S. Pansini 5, 80131 Naples, Italy.
University of Bari Aldo Moro · ITUniversity of Naples Federico II · ITSapienza University of Rome · ITUniversity of Campania "Luigi Vanvitelli" · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oral malignant melanoma (OMM) has a prevalence less than 1% of all melanomas and it commonly develops on the oral mucosa following a slow and unspecific transformation of unstable melanocytic lesions, often resulting in a diagnostic delay. The marker PReferentially Expressed Antigen in MElanoma (PRAME) seems to be a valid tool to investigate the biological and histological nature of cutaneous melanocytic lesions, but to date its use to characterize pigmented lesions in the oral cavity is largely unexplored. The aim of this study was to create preliminary knowledge on the PRAME expression in OMM, and to compare its expression respect to other dysplastic pigmented lesions of the oral cavity. Interestingly, PRAME has been demonstrated to be reliable in the clinical conditions investigated in our pilot study; in fact, it has clearly differentiated the cases of Melanoma, which showed diffuse and intense positivity (score 6+/7+) to PRAME, from the other melanocytic nevi, which resulted to be mainly negative to PRAME. This means a better differential diagnosis, a reliable early diagnosis and a proper clinical/surgical management of the oncological lesions. In conclusion, PRAME can be a valid qualitative marker for differential diagnosis, not only in cutaneous melanomas, but also in malignant melanoma of the entire head and neck area.

Indexed as

Differential Diagnosis.Early diagnosisOral Malignant Melanoma

Identifiers

PMID37057287
PMCPMC10088532
OpenAlexW4324009883

What OpenQuestion holds

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LicenceCC BY
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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.