Evidence map›Paper›PMID 34831313›Full record

SynthesisCells2021

GLUT1, GLUT3 Expression and 18FDG-PET/CT in Human Malignant Melanoma: What Relationship Exists? New Insights and Perspectives.

Gerardo Cazzato, Anna Colagrande, Antonietta Cimmino, Caterina Abbatepaolo, Emilio Bellitti, Paolo Romita, Lucia Lospalluti, Caterina Foti, Francesca Arezzo, Vera Loizzi and 6 more

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Unexpectedly Low FDG and FAPI Uptake in Mucosal Melanoma: Case Report with Literature Review.Indian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India
    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

16 authors at 1 institution in 1 country.

Gerardo CazzatoSection of Pathology, Department of Emergency and Organ Transplantation (DETO), University of Bari, "Aldo Moro", 70124 Bari, Italy.
Anna ColagrandeSection of Pathology, Department of Emergency and Organ Transplantation (DETO), University of Bari, "Aldo Moro", 70124 Bari, Italy.
Antonietta CimminoSection of Pathology, Department of Emergency and Organ Transplantation (DETO), University of Bari, "Aldo Moro", 70124 Bari, Italy.
Caterina AbbatepaoloSection of Pathology, Department of Emergency and Organ Transplantation (DETO), University of Bari, "Aldo Moro", 70124 Bari, Italy.
Emilio BellittiSection of Pathology, Department of Emergency and Organ Transplantation (DETO), University of Bari, "Aldo Moro", 70124 Bari, Italy.ORCID 0000-0001-8959-5773
Paolo RomitaSection of Dermatology, Department of Biomedical Sciences and Human Oncology, University of Bari, "Aldo Moro", 70124 Bari, Italy.
Lucia LospallutiSection of Dermatology, Department of Biomedical Sciences and Human Oncology, University of Bari, "Aldo Moro", 70124 Bari, Italy.
Caterina FotiSection of Dermatology, Department of Biomedical Sciences and Human Oncology, University of Bari, "Aldo Moro", 70124 Bari, Italy.
Francesca ArezzoSection of Ginecology and Obstetrics, Department of Biomedical Sciences and Human Oncology, University of Bari, "Aldo Moro", 70124 Bari, Italy.
Vera LoizziSection of Ginecology and Obstetrics, Department of Biomedical Sciences and Human Oncology, University of Bari, "Aldo Moro", 70124 Bari, Italy.ORCID 0000-0002-4006-6421
Teresa LettiniSection of Pathology, Department of Emergency and Organ Transplantation (DETO), University of Bari, "Aldo Moro", 70124 Bari, Italy.
Sara SabloneSection of Legal Medicine, Department of Interdisciplinary Medicine, Bari Policlinico Hospital, University of Bari, "Aldo Moro", 70124 Bari, Italy.
Leonardo RestaSection of Pathology, Department of Emergency and Organ Transplantation (DETO), University of Bari, "Aldo Moro", 70124 Bari, Italy.ORCID 0000-0003-4335-4776
Gennaro CormioSection of Ginecology and Obstetrics, Department of Biomedical Sciences and Human Oncology, University of Bari, "Aldo Moro", 70124 Bari, Italy.ORCID 0000-0001-5745-372X
Giuseppe IngravalloSection of Pathology, Department of Emergency and Organ Transplantation (DETO), University of Bari, "Aldo Moro", 70124 Bari, Italy.ORCID 0000-0002-4792-3545
Roberta RossiSection of Pathology, Department of Emergency and Organ Transplantation (DETO), University of Bari, "Aldo Moro", 70124 Bari, Italy.
University of Bari Aldo Moro · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMalignant melanoma is the most aggressive of skin cancers and the 19th most common cancer worldwide, with an estimated age-standardized incidence rate of 2.8-3.1 per 100,000; although there have been clear advances in therapeutic treatment, the prognosis of MM patients with Breslow thickness greater than 1 mm is still quite poor today. The study of how melanoma cells manage to survive and proliferate by consuming glucose has been partially addressed in the literature, but some rather interesting results are starting to be present.

methodsA systematic review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and a search of PubMed and Web of Sciences (WoS) databases was performed until 27 September 2021 using the terms: glucose transporter 1 and 3 and GLUT1/3 in combination with each of the following: melanoma, neoplasm and immunohistochemistry.

resultsIn total, 46 records were initially identified in the literature search, of which six were duplicates. After screening for eligibility and inclusion criteria, 16 publications were ultimately included.

conclusionsthe results discussed regarding the role and expression of GLUT are still far from definitive, but further steps toward understanding and stopping this mechanism have, at least in part, been taken. New studies and new discoveries should lead to further clarification of some aspects since the various mechanisms of glucose uptake by neoplastic cells are not limited to the transporters of the GLUT family alone.

Indexed as

Positron Emission Tomography Computed TomographyFluorodeoxyglucose F18Glucose Transporter Type 1Glucose Transporter Type 3HumansMelanomaPublicationsSkin NeoplasmsFluorodeoxyglucose F18Glucose Transporter Type 1Glucose Transporter Type 3GLUT1GLUT3immunohistochemistrymalignant melanomaperspectives

Identifiers

PMID34831313
PMCPMC8624914
OpenAlexW3212477425

What OpenQuestion holds

Textmetadata
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.