Carotenoids from Marine Microalgae as Antimelanoma Agents

被引:14
作者
Alves Ferraz, Christiane Adrielly [1 ]
Grougnet, Raphael [1 ]
Nicolau, Elodie [2 ]
Picot, Laurent [3 ]
de Oliveira Junior, Raimundo Goncalves [1 ]
机构
[1] Univ Paris Cite, Fac Sante, UFR Pharm, UMR 8038 CiTCoM, F-75006 Paris, France
[2] IFREMER, Lab PHYTOX GENALG, F-44311 Nantes, France
[3] La Rochelle Univ, UMR CNRS 7266 LIENSs, F-17042 La Rochelle, France
关键词
marine carotenoids; marine pigments; melanoma; pigments; skin cancer; OPEN-LABEL; ADVANCED MELANOMA; RESISTANCE MECHANISMS; METASTATIC MELANOMA; ACQUIRED-RESISTANCE; GENETIC ALTERATIONS; IMPROVED SURVIVAL; BROWN-ALGAE; IN-VITRO; FUCOXANTHIN;
D O I
10.3390/md20100618
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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-kappa B 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).
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页数:26
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