Cited by 69melanin and skin pigmentationHealthcare and Venom ResearchMelanoma and MAPK Pathways

Helix aspersa maxima mucus exhibits antimelanogenic and antitumoral effects against melanoma cells

Ellijimi, Chedli, Ben Hammouda, Manel, Othman, Houcemeddine, Moslah, Wassim, Jebali, Jed, Mabrouk, Hazem Ben, Morjen, Maram, Haoues, Meriam +4 more·2018·Biomedicine & Pharmacotherapy

Abstract

Snail secretion is currently revolutionizing the world of cosmetics and human skin care. The efficacy of snail secretion in wounds healing has been proven both in vitro and by clinical studies. However, the potential anti-tumor effect of snail secretion was poorly investigated. In this report, our in vitro study showed that Helix aspersa maxima species snail slime (SS) could not only treat melanogenesis but also endowed with anti-tumoral activity against human melanoma cells. Indeed, SS reduced melanin content and tyrosinase activity on B16F10 cells with IC 50 values of 288 μg/mL and 286 μg/mL, respectively, without altering cell viability. This effect was also observed, at a lesser extent, on human melanoma IGR-39 and SK-MEL-28 cell lines. On another hand, SS specifically inhibited the viability of IGR-39 and SK-MEL-28 cells associated to an apoptotic effect highlighted by PARP cleavage. It is worth to note that SS did not affect the viability of B16F10 cells and non tumorigenic HaCaT cells. Interestingly, this extract was found to inhibit migration and invasion of both human melanoma cells through reducing the expression of Matrix metalloproteinase MMP2. Snail slime also exerted a high inhibitory effect on IGR-39 cell adhesion through blocking the function of α 2 β 1 (45%), α v β 3 (38%) integrins and by reducing the expression levels of α v and β 1 integrins. The presented results shed light on the potential anti-melanoma effect of SS and support its use against skin disea…

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Crossref · 10.1016/j.biopha.2018.03.020

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Authors
Ellijimi, C., Ben Hammouda, M., Othman, H., Moslah, W., Jebali, J., Mabrouk, H. B., Morjen, M., Haoues, M., Luis, J., Marrakchi, N., Essafi-Benkhadir, K., & Srairi-Abid, N.
Affiliations
  • Institut Pasteur de Tunis (TN)
  • Inserm (FR)
Venue
Biomedicine & Pharmacotherapy
Publisher
Elsevier BV
Published
2018-05
Volume
101
Pages
871-880
ISSN
0753-3322 (ISSN-L)
OpenAlex
W2790866413
Cited by
69
References
1
Citations by year
2026: 3 · 2025: 13 · 2024: 12 · 2023: 10 · 2022: 9 · 2021: 15 · 2020: 3 · 2019: 3 · 2018: 1
FWCI
3.01
Type
journal article
Language
en
Open access
closed
Locations
  • Biomedicine & Pharmacotherapy (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion)
Funders
  • Tunisian Ministry of Higher Education and Scientific Research (LR11IPT08)
  • National Institute of Health and Medical Research
  • "Partenariat Hubert Curien-Utique (17G 0811)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › melanin and skin pigmentation
  • Health Sciences › Medicine › Pharmacology › Healthcare and Venom Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Melanoma and MAPK Pathways
Keywords
Helix aspersa maxima, snail slime, anti-melanogenic activity, anticancer activity, melanoma, melanogenesis, tyrosinase inhibition, apoptosis, PARP cleavage, cell migration and invasion, MMP-2, integrins, cell adhesion, B16F10 melanoma cells, SK-MEL-28 cells
MeSH terms
Animals, Cell Adhesion, Cell Movement, Cell Survival, Helix, Snails, Humans, Melanins, Melanoma, Mucus, Neoplasm Invasiveness, Apoptosis, Matrix Metalloproteinase 2, Cell Line, Tumor, Matrix Metalloproteinase Inhibitors, Carcinogenesis

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