Journal
JOURNAL OF DERMATOLOGICAL SCIENCE
Volume 106, Issue 3, Pages 170-180Publisher
ELSEVIER IRELAND LTD
DOI: 10.1016/j.jdermsci.2022.05.003
Keywords
Pym-5; GSK-3; Melanogenesis; Melanoma
Categories
Funding
- Jiangsu Province Traditional Chinese Medicine Leading Talents Program Province (China) [SLJ0229]
- Young Scientists Fund of the National Natural Science Foundation of China (China) [81803782]
- Canadian Institutes of Health Research foundation (Canada) [333102]
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The study found that the GSK-3 inhibitor Pym-5 can delay the growth of melanoma cells, promote melanin production, and achieve this effect by activating the Wnt/β-Catenin signaling pathway.
Background: Glycogen synthase kinase-3 (GSK-3) inhibitors are considered to activate Wnt/beta-Catenin, which remains a controversial topic in melanoma treatment.Objective: Here, we have developed Pym-5, an attractive GSK-3 inhibitor. Using Pym-5 as a chemical tool to probe the GSK-3 biology, we aimed to investigate the potential of GSK-3 inhibition as a strategy of melanoma treatment and underlying mechanisms.Methods: Using pigment B16 and B16BL6 murine melanoma model in vitro and a zebrafish pigmentation model in vivo, we investigated Pym-5-meditaed activation of Wnt/beta-Catenin, melanogenesis and antitumor response in melanoma treatment.Results: We found that Pym-5 delayed the growth and promoted melanogenesis of melanoma cells. Pym-5 activated the transcription of beta-Catenin and responsive targets genes (AXIN2 and MITF), melanin biosynthesis genes (TYR, TYRP1 and TYRP2) and eventually elevated the production of melanin. Interestingly, genetic inactivation of GSK-3 beta, but not its paralogue GSK-3 alpha, compromised Pym-5-mediated melanogenesis in B16 and B16BL6 cells.Conclusion: These data provide insight into the potential therapeutic benefits obtained from activation of Wnt/beta-Catenin signaling pathway and how Pym-5 can regulate melanin production and the rationale for future clinical application of GSK-3 inhibitor in melanoma patients.(c) 2022 Japanese Society for Investigative Dermatology. Published by Elsevier B.V. All rights reserved.
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