Abstract

The glaucophyte Cyanophora paradoxa (Cp) was chemically investigated to identify pigments efficiently inhibiting malignant melanoma, mammary carcinoma and lung adenocarcinoma cells growth. Cp water and ethanol extracts significantly inhibited the growth of the three cancer cell lines in vitro, at 100 µg·mL−1. Flash chromatography of the Cp ethanol extract, devoid of c-phycocyanin and allophycocyanin, enabled the collection of eight fractions, four of which strongly inhibited cancer cells growth at 100 µg·mL−1. Particularly, two fractions inhibited more than 90% of the melanoma cells growth, one inducing apoptosis in the three cancer cells lines. The detailed analysis of Cp pigment composition resulted in the discrimination of 17 molecules, ten of which were unequivocally identified by high resolution mass spectrometry. Pheophorbide a, β-cryptoxanthin and zeaxanthin were the three main pigments or derivatives responsible for the strong cytotoxicity of Cp fractions in cancer cells. These data point to Cyanophora paradoxa as a new microalgal source to purify potent anticancer pigments, and demonstrate for the first time the strong antiproliferative activity of zeaxanthin and β-cryptoxanthin in melanoma cells.

Highlights

  • Microalgae have a great potential for the production of bioactive molecules of pharmaceutical interest [1,2,3,4,5]

  • We recently demonstrated the antiproliferative activity of violaxanthin in breast cancer cells, using a bioguided purification strategy [7], and reviewed the anticancer activity of microalgal epoxycarotenoids [6]

  • We here demonstrate that pigments from the glaucocystophyte Cyanophora paradoxa may have interest as anticancer agents, to cure malignant melanomas, which are frequent cancers with bad prognosis

Read more

Summary

Introduction

Microalgae have a great potential for the production of bioactive molecules of pharmaceutical interest [1,2,3,4,5]. Microalgal pigments protect normal cells from genetic damages and exert antiproliferative, cytotoxic and pro-apoptotic activities in cancer cells, suggesting their possible use for cancer prevention or chemiotherapy [6,7,8]. Some pigments cross the lipophilic membranes and may interact with membrane proteins involved in cancer cells multi-drug resistance, or apoptosis. Some inhibit DNA-dependent DNA polymerases, alter the expression of cyclins and CDK, or interfere with major transduction pathways controlling cell survival and transcriptional activation of genes involved in apoptosis, anticancer drugs resistance or. The relevance of microalgae pigments as non-apoptotic cell death inducers, antimetastatic, or inhibitors of cancer cells invasivity or motility, remains to be established. We recently demonstrated the antiproliferative activity of violaxanthin in breast cancer cells, using a bioguided purification strategy [7], and reviewed the anticancer activity of microalgal epoxycarotenoids [6]. We here demonstrate that pigments from the glaucocystophyte Cyanophora paradoxa may have interest as anticancer agents, to cure malignant melanomas, which are frequent cancers with bad prognosis

Antiproliferative Activity of Cp Extracts
Cytotoxic and Pro-Apoptotic Activity of F3 and F5
Characterization of the Cp Fractions
Fraction 8
Experimental Section
Microalgae
RP-HPLC Pigments Analysis
Mass Spectrometry
Cell Culture and Viability Assay
Apoptosis Assay
Conclusions
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call