Evidence map›Paper›PMID 29290903›Full record

ArticleOxidative medicine and cellular longevity2017

Potassium Ascorbate with Ribose: Promising Therapeutic Approach for Melanoma Treatment.

Carlotta Cavicchio, Mascia Benedusi, Erika Pambianchi, Alessandra Pecorelli, Franco Cervellati, Vinno Savelli, Duccio Calamandrei, Emilia Maellaro, Giorgio Rispoli, Emanuela Maioli and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2017. 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
0.8field-weighted citation impact, top 26% 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, 9 citations in OpenAlex.

  1. Inflammasome involvement in CS-induced damage in HaCaT keratinocytes.In vitro cellular & developmental biology. Animal · 2022
    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 at 3 institutions in 2 countries.

Carlotta CavicchioDepartment of Life Sciences and Biotechnology, University of Ferrara, Ferrara, Italy.
Mascia BenedusiDepartment of Life Sciences and Biotechnology, University of Ferrara, Ferrara, Italy.
Erika PambianchiPlants for Human Health Institute, Department of Animal Sciences, North Carolina State University, Kannapolis, NC, USA.
Alessandra PecorelliPlants for Human Health Institute, Department of Animal Sciences, North Carolina State University, Kannapolis, NC, USA.ORCID 0000-0002-5207-068X
Franco CervellatiDepartment of Life Sciences and Biotechnology, University of Ferrara, Ferrara, Italy.ORCID 0000-0002-0051-2597
Vinno SavelliDepartment of Medicine, Surgery and Neurosciences, University of Siena, Siena, Italy.
Duccio CalamandreiDepartment of Biotechnology, Chemistry and Pharmacy, University of Siena, Siena, Italy.
Emilia MaellaroDepartment of Molecular and Developmental Medicine, University of Siena, Siena, Italy.
Giorgio RispoliDepartment of Life Sciences and Biotechnology, University of Ferrara, Ferrara, Italy.ORCID 0000-0002-9390-5620
Emanuela MaioliDepartment of Life Sciences, University of Siena, Siena, Italy.
Giuseppe ValacchiDepartment of Life Sciences and Biotechnology, University of Ferrara, Ferrara, Italy.ORCID 0000-0002-8792-0947
University of Ferrara · ITUniversity of Siena · ITNorth Carolina State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While surgery is the definitive treatment for early-stage melanoma, the current therapies against advanced melanoma do not yet provide an effective, long-lasting control of the lesions and a satisfactory impact on patient survival. Thus, research is also focused on novel treatments that could potentiate the current therapies. In the present study, we evaluated the effect of potassium ascorbate with ribose (PAR) treatment on the human melanoma cell line, A375, in 2D and 3D models. In the 2D model, in line with the current literature, the pharmacological treatment with PAR decreased cell proliferation and viability. In addition, an increase in Connexin 43 mRNA and protein was observed. This novel finding was confirmed in PAR-treated melanoma cells cultured in 3D, where an increase in functional gap junctions and a higher spheroid compactness were observed. Moreover, in the 3D model, a remarkable decrease in the size and volume of spheroids was observed, further supporting the treatment efficacy observed in the 2D model. In conclusion, our results suggest that PAR could be used as a safe adjuvant approach in support to conventional therapies for the treatment of melanoma.

Indexed as

Antineoplastic AgentsAscorbic AcidCell Line, TumorCell ProliferationCell SurvivalConnexin 43HumansMelanomaMicroscopy, Electron, ScanningPotassiumRiboseSpheroids, CellularAntineoplastic AgentsAscorbic AcidConnexin 43PotassiumRibose

Identifiers

PMID29290903
PMCPMC5632911
OpenAlexW2757818983

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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.