Halamphora sp. Reduces Inflammation in LPS-Stimulated Human Malignant Melanoma and Immortalized Keratinocytes Influencing TNF-α Release
Eleonora Montuori, Espen Holst Hansen, Calum J. McMullen, Katja Rietdorf, Carlos Almeida, Antera Martel Quintana, Assunta Saide, Chiara Lauritano

TL;DR
A microalgae species reduces inflammation in melanoma and skin cells, potentially offering new anti-inflammatory treatments.
Contribution
First report of Halamphora sp.'s anti-melanoma and anti-inflammatory effects and its biotechnological potential.
Findings
Fraction D from Halamphora sp. reduces inflammation in LPS-stimulated melanoma and keratinocyte cells.
Hydroxypheophorbide a, a chlorophyll breakdown product, is identified as a key compound in the bioactive fraction.
Treatment with fraction D down-regulates inflammatory pathways in melanoma and keratinocyte cells.
Abstract
Malignant melanoma is skin cancer arising from genetically altered melanocytes. Recently, a complex relationship between melanoma and chronic inflammation has been highlighted, representing an excellent condition for tumor development. Microalgae have been shown to be a promising source of bioactive compounds for drug discovery. In this study, we investigated Halamphora sp. (BEA0050) to identify possible compounds with immunomodulatory activity. The most active fraction (fraction D) showed anti-inflammatory activity against human melanoma cancer cells (A2058) stimulated using lipopolysaccharide (LPS) to induce an inflammatory phenotype. Chemical profiling of the bioactive fraction using chromatography and high-resolution mass spectrometry (UHPLC-HR-MS) revealed hydroxypheophorbide a, a breakdown product of chlorophyll a. In order to investigate the mechanism of action, the TNF-α release…
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Taxonomy
TopicsSeaweed-derived Bioactive Compounds · Biological Research and Disease Studies · Algal biology and biofuel production
