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In Vitro Anticancer Activity of a Nonpolar Fraction from Gynostemma pentaphyllum (Thunb.) Makino

机译:绞股蓝(Mynino)的非极性级分的体外抗癌活性

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摘要

Gynostemma pentaphyllum (Thunb.) Makino (GpM) has been widely used in traditional Chinese medicine (TCM) for the treatment of various diseases including cancer. Most previous studies have focused primarily on polar fractions of GpM for anticancer activities. In this study, a nonpolar fraction EA1.3A from GpM showed potent growth inhibitory activities against four cancer cell lines with IC50 ranging from 31.62 μg/mL to 38.02 μg/mL. Furthermore, EA1.3A also inhibited the growth of breast cancer cell MDA-MB-453 time-dependently, as well as its colony formation ability. EA1.3A induced apoptosis on MDA-MB-453 cells both dose-dependently and time-dependently as analyzed by flow cytometry and verified by western blotting analysis of apoptosis marker cleaved nuclear poly(ADP-ribose) polymerase (cPARP). Additionally, EA1.3A induced cell cycle arrest in G0/G1 phase. Chemical components analysis of EA1.3A by GC-MS revealed that this nonpolar fraction from GpM contains 10 compounds including four alkaloids, three organic esters, two terpenes, and one catechol substance, and all these compounds have not been reported in GpM. In summary, the nonpolar fraction EA1.3A from GpM inhibited cancer cell growth through induction of apoptosis and regulation of cell cycle progression. Our study shed light on new chemical bases for the anticancer activities of GpM and feasibilities to develop new anticancer agents from this widely used medicinal plant.
机译:绞股蓝绞股蓝(Thunb。)Makino(GpM)已广泛用于传统中药(TCM),用于治疗包括癌症在内的各种疾病。以前的大多数研究主要集中在GpM的极性部分上以达到抗癌活性。在这项研究中,来自GpM的非极性级分EA1.3A显示出对四种癌细胞系的有效生长抑制活性,IC50为31.62μg/ mL至38.02μg/ mL。此外,EA1.3A还具有时间依赖性地抑制乳腺癌细胞MDA-MB-453的生长及其集落形成能力。 EA1.3A诱导MDA-MB-453细胞凋亡,无论是剂量依赖性还是时间依赖性,均通过流式细胞术进行分析,并通过Western blotting验证凋亡标记物切割的核聚ADP-核糖聚合酶(cPARP)。此外,EA1.3A诱导细胞周期停滞在G0 / G1期。通过GC-MS对EA1.3A进行化学成分分析表明,来自GpM的非极性馏分包含10种化合物,包括四种生物碱,三种有机酯,两种萜烯和一种儿茶酚物质,而所有这些化合物均未在GpM中报道。总之,来自GpM的非极性级分EA1.3A通过诱导细胞凋亡和调节细胞周期进程来抑制癌细胞的生长。我们的研究为GpM的抗癌活性提供了新的化学基础,并为从这种广泛使用的药用植物开发新的抗癌剂提供了可能性。

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