Cancer Cell Inhibiting Sea Cucumber (<i>Holothuria leucospilota</i>) Protein as a Novel Anti-Cancer Drug

Cancer remains the primary cause of death worldwide. To develop less toxic anti-cancer drugs to relieve the suffering and improve the survival of cancer patients is the major focus in the anti-cancer field. To this end, marine creatures are being extensively studied for their anti-cancer effects, si...

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Main Authors: Ruizhen Ru, Yanzheng Guo, Juanxuan Mao, Zonghe Yu, Wen Huang, Xudong Cao, Huijian Hu, Minjie Meng, Lihong Yuan
Format: Article
Language:English
Published: MDPI AG 2022-02-01
Series:Nutrients
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Online Access:https://www.mdpi.com/2072-6643/14/4/786
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Summary:Cancer remains the primary cause of death worldwide. To develop less toxic anti-cancer drugs to relieve the suffering and improve the survival of cancer patients is the major focus in the anti-cancer field. To this end, marine creatures are being extensively studied for their anti-cancer effects, since extracts from at least 10% of the marine organisms have been shown to possess anti-tumor activities. As a classic Chinese traditional medicine, sea cucumbers and compounds extracted from the sea cucumbers, such as polysaccharides and saponins, have recently been shown to exhibit anti-cancer, anti-inflammatory, and anti-oxidant effects. <i>Holothuria leucospilota</i> (<i>H. leucospilota</i>) is a tropical edible sea cucumber species that has been successfully cultivated and farmed in large scales, providing a readily available source of raw materials to support the development of novel marine anti-cancer drugs. However, very few studies have so far been performed on the biological activities of <i>H. leucospilota</i>. In this study, we first investigated the anti-cancer effect of <i>H. leucospilota</i> protein on three cancer cell lines (i.e., HepG2, A549, Panc02) and three normal cell lines (NIH-3T3, HaCaT, 16HBE). Our data showed that <i>H. leucospilota</i> protein decreased the cell viabilities of HepG2, A549, HaCaT, 16HBE in a concentration-dependent manner, while Panc02 and NIH-3T3 in a time- and concentration-dependent manner. We also found that the inhibitory effect of <i>H. leucospilota</i> protein (≥10 μg/mL) on cell viability is near or even superior to EPI, a clinical chemotherapeutic agent. In addition, our data also demonstrated that <i>H. leucospilota</i> protein significantly affected the cell cycle and induced apoptosis in the three cancer cell lines investigated; in comparison, it showed no effects on the normal cell lines (i.e., NIH-3T3, HaCaT and 16HBE). Finally, our results also showed that <i>H. leucospilota</i> protein exhibited the excellent performance in inhibiting cell immigrations. In conclusion, <i>H. leucospilota</i> protein targeted the cancer cell cycles and induced cancer cell apoptosis; its superiority to inhibit cancer cell migration compared with EPI, shows the potential as a promising anti-cancer drug.
ISSN:2072-6643