Carotenoids from Marine Microalgae as Antimelanoma Agents.
Christiane Adrielly Alves FerrazRaphaël GrougnetElodie NicolauLaurent PicotRaimundo Gonçalves de Oliveira JuniorPublished in: Marine drugs (2022)
Melanoma cells are highly invasive and metastatic tumor cells and commonly express molecular alterations that contribute to multidrug resistance (e.g., BRAF V600E mutation). Conventional treatment is not effective in a long term, requiring an exhaustive search for new alternatives. Recently, carotenoids from microalgae have been investigated as adjuvant in antimelanoma therapy due to their safety and acceptable clinical tolerability. Many of them are currently used as food supplements. In this review, we have compiled several studies that show microalgal carotenoids inhibit cell proliferation, cell migration and invasion, as well as induced cell cycle arrest and apoptosis in various melanoma cell lines. MAPK and NF-ĸB pathway, MMP and apoptotic factors are frequently affected after exposure to microalgal carotenoids. Fucoxanthin, astaxanthin and zeaxanthin are the main carotenoids investigated, in both in vitro and in vivo experimental models. Preclinical data indicate these compounds exhibit direct antimelanoma effect but are also capable of restoring melanoma cells sensitivity to conventional chemotherapy (e.g., vemurafenib and dacarbazine).
Keyphrases
- cell cycle arrest
- pi k akt
- cell death
- cell proliferation
- signaling pathway
- oxidative stress
- cell therapy
- small cell lung cancer
- single cell
- atomic force microscopy
- diabetic rats
- early stage
- endoplasmic reticulum stress
- cell cycle
- anaerobic digestion
- clinical trial
- randomized controlled trial
- mesenchymal stem cells
- big data
- locally advanced
- single molecule
- bone marrow
- case control
- metastatic colorectal cancer
- smoking cessation
- double blind
- wild type