LC-ESI-MS/MS analysis of phenolic compounds and in vitro cytotoxicity and apoptosis-inducing effects of Nonea pulmonarioides extracts

IF 1.9 3区 化学 Q3 CHEMISTRY, APPLIED
Fuad O. Abdullah , Haval H. Muhammed , Mustafa Abdullah Yilmaz , Oguz Cakir , Abbas Tarhan
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Abstract

The chemical composition of Nonea pulmonarioides extracts were investigated for the first time. The phytoconstituents of the methanol extracts were screened by using LC/MS-MS technique. The anticancer activity of the acetone and methanol extracts were measured against four cancer cell lines; MCF-7, PC3, HT-29, and U-87 MG. Thirty phenolic compounds were identified, rosmarinic (90.06 mg analyte/g extract) and fumaric acids (39.737 mg analyte/g extract) were major compounds of the studied species. Moreover, both methanol and acetone extracts were found to have strong anticancer activities. The acetone extract HT-29 (with IC50 of 10.17 ± 0.25 µg/mL) compared with standard cis-platin (with IC50 of 22.20 ± 0.72 µg/mL) with apoptotic mediated programmed cell death. These findings identified N. pulmonarioides as a potential species exhibiting anticancer properties. In conclusion, the compelling results show that the methanol extract contains possible bioactive compounds with anticancer properties that require isolation and further characterisation.
LC-ESI-MS/MS分析酚类化合物以及Nonea pulmonarioides提取物的体外细胞毒性和细胞凋亡诱导效应。
首次研究了Nonea pulmonarioides提取物的化学成分。采用 LC/MS-MS 技术筛选了甲醇提取物中的植物成分。测定了丙酮和甲醇提取物对 MCF-7、PC3、HT-29 和 U-87 MG 四种癌细胞株的抗癌活性。共鉴定出 30 种酚类化合物,其中迷迭香酸(90.06 毫克分析物/克提取物)和富马酸(39.737 毫克分析物/克提取物)是所研究物种的主要化合物。此外,甲醇和丙酮提取物都具有很强的抗癌活性。丙酮提取物 HT-29(IC50 为 10.17 ± 0.25 µg/mL)与标准顺铂(IC50 为 22.20 ± 0.72 µg/mL)相比,具有细胞凋亡介导的程序性细胞死亡作用。这些研究结果表明,N. pulmonarioides 是一种具有抗癌特性的潜在物种。总之,令人信服的结果表明,甲醇提取物中可能含有具有抗癌特性的生物活性化合物,需要对其进行分离和进一步鉴定。
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来源期刊
Natural Product Research
Natural Product Research 化学-医药化学
CiteScore
5.10
自引率
9.10%
发文量
605
审稿时长
2.1 months
期刊介绍: The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds. The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal. Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section. All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.
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