Evidence map›Paper›PMID 35565448›Full record

ArticleCancers2022

Prognostic Value of IGF2 mRNA-Binding Protein 3 (IGF2BP3) Intratumoral Expression in Melanoma Patients at the Time of Diagnosis: Comparative Analysis of RT-qPCR Versus Immunohistochemistry.

Beatriz Sánchez-Sendra, Silvia Pérez-Debén, José F González-Muñoz, Amelia Murgui, Carlos Monteagudo

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 2 institutions in 1 country.

Beatriz Sánchez-SendraDepartment of Pathology, University of Valencia, 46010 Valencia, Spain.ORCID 0000-0002-9115-9249
Silvia Pérez-DebénOncology Area, Skin Cancer Research Group, Biomedical Research Institute INCLIVA, 46010 Valencia, Spain.
José F González-MuñozOncology Area, Skin Cancer Research Group, Biomedical Research Institute INCLIVA, 46010 Valencia, Spain.ORCID 0000-0002-9832-3355
Amelia MurguiDepartment of Biochemistry and Molecular Biology, University of Valencia, 46100 Valencia, Spain.
Carlos MonteagudoDepartment of Pathology, University of Valencia, 46010 Valencia, Spain.ORCID 0000-0002-9381-9976
Universitat de València · ESINCLIVA Health Research Institute · ES

Funding

Asociación Española Contra el Cáncer Proyecto Everest DonationGeneralitat Valenciana PROMETEO II/2015/009Instituto de Salud Carlos III, Spain; FEDER European funds PI17/02019Instituto de Salud Carlos III, Spain; FEDER European funds PI20/00094
6 · The paper itself

Abstract

Screening for prognostic biomarkers is crucial for clinical melanoma management. Insulin-like growth factor-II mRNA-binding protein 3 (IGF2BP3) has emerged as a potential melanoma diagnostic and prognostic biomarker. It is commonly tested by immunohistochemistry (IHC). Our study retrospectively examines IGF2BP3 mRNA and protein expression in primary melanomas, their correlation with clinicopathologic factors, clinical outcome, and selected miRNAs expression, and their efficiency in predicting melanoma progression and survival. RT-qPCR and IHC on IGF2BP3 expression were performed in 61 cryopreserved and 63 formalin-fixed paraffin-embedded primary melanomas, respectively, and correlated to clinicopathologic factors, distant metastasis-free survival (DMFS), and melanoma -specific survival (MSS). The correlation between RT-qPCR and IHC was significant but moderate. IGF2BP3 mRNA showed a stronger association with clinicopathologic factors (Breslow thickness, ulceration, mitosis rate, growth phase, development of metastasis, and melanoma-specific survival) than its protein counterpart. Interestingly, higher IGF2BP3 mRNA expression was detected in primary melanomas that further metastasized to distant sites and was an independent prognostic factor for the risk of unfavorable DMFS and MSS. RT-qPCR outperformed IHC in sensitivity and in predicting worse clinical outcomes. Therefore, RT-qPCR may successfully be implemented for routine IGF2BP3 assessing for the selection of melanoma patients with a higher risk of developing distant metastasis and dying of melanoma.

Indexed as

biomarkersdistant metastasisIGF2BP3IHCmelanomaRT-qPCR

Identifiers

PMID35565448
PMCPMC9100051
OpenAlexW4229333478

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.