Evidence map›Paper›PMID 40040652›Full record

ArticleToxicology research2025

Comparative in vitro and in silico evaluation of the toxic effects of metformin and/or ascorbic acid, new treatment options in the treatment of Melasma.

Hülya Tezel Yalçın, Deniz Arca Çakır, Anıl Yirün, Sonia Sanajou, Gözde Işık, Özlem Bozdemir, İbrahim Özçelik, Merve Güdül Bacanlı, Naciye Dilara Zeybek, Terken Baydar and 1 more

Abstract read
In one paragraph

Article in Toxicology research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Hülya Tezel YalçınHacettepe University Faculty of Pharmacy, Department of Pharmaceutical Toxicology, Sıhhiye Ankara 06100, Turkey.ORCID https://orcid.org/0000-0002-1843-3424
Deniz Arca ÇakırHacettepe University Vaccine Institute, Department of Vaccine Technology, Sıhhiye Ankara 06100, Turkey.
Anıl YirünÇukurova University Faculty of Pharmacy, Department of Pharmaceutical Toxicology, Balcalı Sarıçam 01250 Adana, Turkey.
Sonia SanajouHacettepe University Faculty of Pharmacy, Department of Pharmaceutical Toxicology, Sıhhiye Ankara 06100, Turkey.
Gözde IşıkHacettepe University Vaccine Institute, Department of Vaccine Technology, Sıhhiye Ankara 06100, Turkey.
Özlem BozdemirHacettepe University Faculty of Medicine, Department of Histology and Embryology, Sıhhiye Ankara 06100, Turkey.
İbrahim ÖzçelikFaculty of Pharmacy, Department of Toxicology, Erzincan Binali Yildirim University, Yalnızbağ Erzincan 24002, Turkey.
Merve Güdül BacanlıFaculty of Pharmacy, Department of Toxicology, Health Sciences University, Keçiören, Ankara 06010, Turkey.ORCID https://orcid.org/0000-0001-8757-0572
Naciye Dilara ZeybekHacettepe University Faculty of Medicine, Department of Histology and Embryology, Sıhhiye Ankara 06100, Turkey.
Terken BaydarHacettepe University Faculty of Pharmacy, Department of Pharmaceutical Toxicology, Sıhhiye Ankara 06100, Turkey.
Pınar ErkekoğluHacettepe University Faculty of Pharmacy, Department of Pharmaceutical Toxicology, Sıhhiye Ankara 06100, Turkey.ORCID https://orcid.org/0000-0003-4713-7672

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melasma is a chronic condition that leads to the buildup of melanin pigment in the epidermis and dermis due to active melanocytes. Even though it is considered a non-life-threatening condition, pigment disorders have a negative impact on quality of life. Since melasma treatment is not sufficient and complicated, new treatment options are sought. Research on metformin and ascorbic acid suggested that they might be used against melasma in the scope of "drug repositioning."The MNT-1 human melanoma cell line was used to assess the effects of metformin, ascorbic acid, and metformin+ascorbic acid combination on cytotoxicity and oxidative stress. Melanin, cAMP, L-3,4-dihydroxyphenylalanine (L-DOPA) and tyrosinase levels were determined by commercial ELISA kits and tyrosinase gene expression was analyzed with RT-qPCR. Cytopathological evaluations were performed by phase contrast microscopy. Tyrosinase expression was determined by immunofluorescence (IF) staining of MNT-1 cells. The online service TargetNet was used for biological target screening. The parameters were not significantly altered by ascorbic acid applied at non-cytotoxic concentrations. On the contrary, metformin dramatically raised tyrosinase and intracellular ROS levels. Moreover, intracellular ROS levels and tyrosinase levels were found to be considerably elevated with the combined treatment. Also, potential metformin and ascorbic acid interactions were determined. According to the results, it can be said that these parameters were not significantly altered by ascorbic acid. On the contrary, metformin dramatically raised tyrosinase and intracellular oxidative stress levels. Moreover, intracellular oxidative stress and tyrosinase levels were elevated with the combined treatment. In conclusion, individual treatments of ascorbic acid or metformin may only provide a limited effect when treating melasma and extensive in vitro and in vivo research are required.

Indexed as

ascorbic acidhyperpigmentationIn silicoIn vitrometforminMNT-1 cells

Identifiers

PMID40040652
PMCPMC11878769

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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.