Evidence map›Paper›PMID 38893077›Full record

ArticleCancers2024

Mutational Profiles of Cutaneous Squamous Cell Carcinomas with Different Patterns of Clinical Aggression from Head and Neck Regions.

Maria Colombino, Giuseppe Palmieri, Manuela Rodio, Matilde Tettamanzi, Silvia Rampazzo, Raffaello Margani, Emilio Trignano, Antonio Cossu, Maria Antonietta Fedeli, Giovanni Maria Fadda and 1 more

Abstract read
In one paragraph

Article in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
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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

11 authors.

Maria ColombinoInstitute of Genetic and Biomedical Research (IRGB), National Research Council (CNR), 07100 Sassari, Italy.
Giuseppe PalmieriImmuno-Oncology & Targeted Cancer Biotherapies, Unit of Cancer Genetics, Institute of Genetic and Biomolecular Research, National Research Council (CNR), University of Sassari, 07100 Sassari, Italy.ORCID 0000-0002-4350-2276
Manuela RodioPlastic Surgery Unit, University Hospital Trust of Sassari, 07100 Sassari, Italy.ORCID 0000-0002-4001-1009
Matilde TettamanziPlastic Surgery Unit, University Hospital Trust of Sassari, 07100 Sassari, Italy.ORCID 0000-0003-2985-5902
Silvia RampazzoPlastic Surgery Unit, University Hospital Trust of Sassari, 07100 Sassari, Italy.
Raffaello MarganiPlastic Surgery Unit, University Hospital Trust of Sassari, 07100 Sassari, Italy.
Emilio TrignanoPlastic Surgery Unit, University Hospital Trust of Sassari, 07100 Sassari, Italy.
Antonio CossuUnit of Anatomic Pathology and Histology, University Hospital of Sassari (A.O.U. SS), Via Matteotti 60, 07100 Sassari, Italy.
Maria Antonietta FedeliUnit of Anatomic Pathology and Histology, University Hospital of Sassari (A.O.U. SS), Via Matteotti 60, 07100 Sassari, Italy.ORCID 0000-0002-0206-6658
Giovanni Maria FaddaOncologia Medica, University Hospital of Sassari (A.O.U. SS), 07100 Sassari, Italy.
Corrado RubinoPlastic Surgery Unit, University Hospital Trust of Sassari, 07100 Sassari, Italy.ORCID 0000-0002-2410-6083

Funding

Fondazione di Sardegna J85F21001150007
6 · The paper itself

Abstract

Cutaneous squamous cell carcinoma is a prevalent malignancy with a rising incidence and a notably high mutational load. Exploring the genetic nuances of cSCC and investigating molecular approaches stands as a potential avenue for improving outcomes in high-risk patients. This retrospective case-control study involved two cohorts, one of 14 patients (the "discovery cohort") and the other of 12 patients (the "validation cohort"), with cSCC located in the head/neck anatomical region and diagnosed at the pT2 stage. Overall, cases developed early local relapses of the disease, whereas controls never relapsed during the entire follow-up period. A next-generation sequencing (NGS) approach conducted on histological samples revealed that TP53 and CDKN2A were the most frequently mutated genes in our series. No specific mutations were identified as potential prognostic or therapeutic targets. Controls exhibited a tendency toward a higher mutational rate compared to cases. It is possible that an increased number of mutations could prompt the cSCC to expose more antigens, becoming more immunogenic and facilitating recognition by the immune system. This could enhance and sustain the immunological response, potentially preventing future recurrences.

Indexed as

cutaneous squamous cell carcinoma (cSCC)immunogenicitymutation profilenext-generation sequencing (NGS)non-melanoma skin cancerrecurrent cSCC

Identifiers

PMID38893077
PMCPMC11171166

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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.