Evidence map›Paper›PMID 30454024›Full record

ArticleJournal of experimental & clinical cancer research : CR2018

Semaphorin 5A drives melanoma progression: role of Bcl-2, miR-204 and c-Myb.

Simona D'Aguanno, Elisabetta Valentini, Maria Grazia Tupone, Marianna Desideri, Marta Di Martile, Manuela Spagnuolo, Simonetta Buglioni, Cristiana Ercolani, Italia Falcone, Marco De Dominici and 7 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. BCL-2 and BCL-xL in Cancer: Regulation, Function, and Therapeutic Targeting.International journal of molecular sciences · 2026
    Review
  2. Article
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  4. RhoG-Binding Domain of Elmo1 Ameliorates Excessive Process Elongation Induced by Autism Spectrum Disorder-Associated Sema5A.Pathophysiology : the official journal of the International Society for Pathophysiology · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. SEMAPHORINS and their receptors: focus on the crosstalk between melanoma and hypoxia.Journal of experimental & clinical cancer research : CR · 2021
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. miRNAs in the Diagnosis and Prognosis of Skin Cancer.Frontiers in cell and developmental biology · 2020
    Review
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

17 authors at 4 institutions in 2 countries.

Simona D'AguannoPreclinical Models and New Therapeutic Agents Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy. simona.daguanno@ifo.gov.it.
Elisabetta ValentiniPreclinical Models and New Therapeutic Agents Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Maria Grazia TuponePreclinical Models and New Therapeutic Agents Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Marianna DesideriPreclinical Models and New Therapeutic Agents Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Marta Di MartilePreclinical Models and New Therapeutic Agents Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Manuela SpagnuoloOncogenomic and Epigenetic Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Simonetta BuglioniPathology Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Cristiana ErcolaniPathology Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Italia FalconeMedical Oncology 1, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Marco De DominiciDepartment of Cancer Biology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.
Michele MilellaMedical Oncology 1, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Maria Giulia RizzoOncogenomic and Epigenetic Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Bruno CalabrettaDepartment of Cancer Biology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.
Carlo CotaDermatopathology Unit, IRCCS San Gallicano Dermatological Institute, Rome, Italy.
Andrea AnichiniFondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Daniela TrisciuoglioPreclinical Models and New Therapeutic Agents Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Donatella Del BufaloPreclinical Models and New Therapeutic Agents Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy. donatella.delbufalo@ifo.gov.it.
Istituti di Ricovero e Cura a Carattere Scientifico · ITThomas Jefferson University · USFondazione IRCCS Istituto Nazionale dei Tumori · ITSan Gallicano Hospital · IT

Funding

Italian Association for Cancer Research IG 18560
6 · The paper itself

Abstract

backgroundMelanoma, the most aggressive form of skin cancer, is characterized by high rates of metastasis, drug resistance and mortality. Here we investigated the role of Semaphorin 5A (Sema5A) on the properties associated with melanoma progression and the factors involved in Sema5A regulation.

methodsWestern blotting, qRT-PCR, Chromatin immunoprecipitation (ChIP) assay, immunohistochemistry of melanoma patient specimens and xenograft tissues, in vitro Transwell assay for cell migration and invasion evaluation, in vitro capillary-like structure formation analysis.

resultsA significant correlation of Sema5A mRNA expression and melanoma progression was observed by analyzing GEO profile dataset. Endogenous Sema5A protein was detected in 95% of human melanoma cell lines tested, in 70% of metastatic specimens from patients affected by melanoma, and 16% of in situ melanoma specimens showed a focal positivity. We demonstrated that Sema5A regulates in vitro cell migration and invasion and the formation of vasculogenic structures. We also found an increase of Sema5A at both mRNA and protein level after forced expression of Bcl-2. By use of transcriptional and proteasome inhibitors, we showed that Bcl-2 increases the stability of Sema5A mRNA and protein. Moreover, by ChIP we demonstrated that Sema5A expression is under the control of the transcription factor c-Myb and that c-Myb recruitment on Sema5A promoter is increased after Bcl-2 overexpression. Finally, a concomitant decrease in the expression of Sema5A, Bcl-2 and c-Myb proteins was observed in melanoma cells after miR-204 overexpression.

conclusionOverall our data provide evidences supporting the role of Sema5A in melanoma progression and the involvement of Bcl-2, miR-204 and c-Myb in regulating its expression.

Indexed as

AnimalsCell Line, TumorDisease ProgressionFemaleHumansMelanomaMembrane ProteinsMiceMice, NudeMicroRNAsNerve Tissue ProteinsProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-mybSemaphorinsSkin NeoplasmsTransfectionBCL2 protein, humanMembrane ProteinsMicroRNAsMIRN204 microRNA, humanNerve Tissue ProteinsProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-mybSEMA5A protein, humanSemaphorinsBcl-2c-MybMelanomamiR-204Semaphorin 5A

Identifiers

PMID30454024
PMCPMC6245779
OpenAlexW2901856936

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.