Natural Products from Mangroves: An Overview of the Anticancer Potential of Avicennia marina

被引:10
作者
Cerri, Federico [1 ]
Giustra, Marco [2 ]
Anadol, Yaprak [3 ]
Tomaino, Giulia [2 ]
Galli, Paolo [1 ,3 ,4 ]
Labra, Massimo [2 ]
Campone, Luca [2 ]
Colombo, Miriam [2 ]
机构
[1] Univ Milano Bicocca, Dept Earth & Environm Sci, I-20126 Milan, Italy
[2] Univ Milano Bicocca, Dept Biotechnol & Biosci, I-20126 Milan, Italy
[3] Univ Dubai, Dubai Business Sch, Dubai 14143, U Arab Emirates
[4] Marine Res & High Educ MaRHE Ctr, Magoodhoo Isl 12030, Faafu Atoll, Maldives
关键词
Avicennia marina; cytotoxicity; anticancer activity; natural products; bioactive natural compounds; bioprospecting; IRIDOID GLUCOSIDES; GREY MANGROVE; LEAF EXTRACT; TRITERPENOIDS; LEAVES;
D O I
10.3390/pharmaceutics14122793
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Exploring the potential of natural extracts for pharmaceutical applications in the treatment of different diseases is an emerging field of medical research, owing to the tremendous advantages that they can offer. These include compound sustainability due to the natural origin and virtually unlimited availability. In addition, they contribute to promoting the countries in which they are extracted and manufactured. For this reason, wild active compounds derived from plants are attracting increasing interest due to their beneficial properties. Among them, Avicennia marina has been recently recognized as a potential source of natural substances with therapeutic activities for anti-cancer treatment. A. marina beneficially supplies different chemical compounds, including cyclic triterpenoids, flavonoids, iridoids, naphtaquinones, polyphenols, polysaccharides, and steroids, most of them exhibiting potent antitumor activity. The in vivo and in vitro studies on different models of solid tumors demonstrated its dose-dependent activity. Moreover, the possibility to formulate the A. marina extracted molecules in nanoparticles allowed researchers to ameliorate the therapeutic outcome of treatments exploiting improved selectivity toward cancer cells, thus reducing the side effects due to nonspecific spread.
引用
收藏
页数:12
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