Palanisamy Satheesh Kumar, Trisciuoglio Daniela, Zwergel Clemens, Del Bufalo Donatella, Mai Antonello
a Department of Chemical, Biological, Pharmaceutical and Environmental Science , University of Messina , Messina , Italy.
b Department of Research, Advanced Diagnostics and Technological Innovation , Regina Elena National Cancer Institute , Rome , Italy.
J Enzyme Inhib Med Chem. 2017 Dec;32(1):614-623. doi: 10.1080/14756366.2016.1266344.
To identify the metabolite distribution in ascidian, we have applied an integrated liquid chromatography- tandem mass spectrometry (LC-MS) metabolomics approach to explore and identify patterns in chemical diversity of invasive ascidian Styela plicata. A total of 71 metabolites were reported among these alkaloids, fatty acids and lipids are the most dominant chemical group. Multivariate statistical analysis, principal component analysis (PCA) showed a clear separation according to chemical diversity and taxonomic groups. PCA and partial least square discriminant analysis were applied to discriminate the chemical group of S. plicata crude compounds and classify the compounds with unknown biological activities. In this study, we reported for the first time that a partially purified methanol extract prepared from the ascidian S. plicata and Ascidia mentula possess antitumor activity against four tumor cell lines with different tumor histotype, such as HeLa (cervical carcinoma), HT29 (colon carcinoma), MCF-7 (breast carcinoma) and M14 (melanoma). S. plicata fraction SP-50 showed strong inhibition of cell proliferation and induced apoptosis in HeLa and HT29 cells, thus indicating S. plicata fraction SP-50 a potential lead compound for anticancer therapy. The molecular mechanism of action and chemotherapeutic potential of these ascidian unknown biomolecules need further research.
为了确定海鞘中的代谢物分布,我们应用了一种综合液相色谱 - 串联质谱(LC-MS)代谢组学方法,以探索和识别入侵性海鞘皱瘤海鞘化学多样性的模式。在这些生物碱中总共报告了71种代谢物,脂肪酸和脂质是最主要的化学类别。多变量统计分析,主成分分析(PCA)根据化学多样性和分类学组显示出明显的分离。应用PCA和偏最小二乘判别分析来区分皱瘤海鞘粗化合物的化学类别,并对具有未知生物活性的化合物进行分类。在本研究中,我们首次报道从皱瘤海鞘和海鞘制备的部分纯化甲醇提取物对四种具有不同肿瘤组织类型的肿瘤细胞系具有抗肿瘤活性,例如HeLa(宫颈癌)、HT29(结肠癌)、MCF-7(乳腺癌)和M14(黑色素瘤)。皱瘤海鞘组分SP-50对HeLa和HT29细胞中的细胞增殖具有强烈抑制作用并诱导凋亡,因此表明皱瘤海鞘组分SP-50是一种潜在的抗癌治疗先导化合物。这些海鞘未知生物分子的作用分子机制和化疗潜力需要进一步研究。