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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >In Vitro Anticancer Activity of a Nonpolar Fraction from Gynostemma pentaphyllum (Thunb.) Makino
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In Vitro Anticancer Activity of a Nonpolar Fraction from Gynostemma pentaphyllum (Thunb.) Makino

机译:来自古脑脑枢头枢纽术(THUNB)的非极性分数的体外抗癌活性(THUNB。)Makino

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摘要

Gynostemma pentaphyllum(Thunb.) Makino (GpM) has beenwidely used in traditional Chinesemedicine (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 from31.62 mu g/mL to 38.02 mu g/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 dosedependently 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:Gynostemma pentaphyllum(Thunb。)Makino(GPM)已经过度用于传统的ChineEmedicine(TCM),用于治疗包括癌症的各种疾病。最先前的研究主要集中在抗癌活动中的GPM极性分数上。在该研究中,来自GPM的非极性分数EA1.3a显示出对4个癌细胞系的有效的生长抑制活性,IC50范围为31.62μg/ ml至38.02μg/ ml。此外,EA1.3a还依靠持续时间抑制乳腺癌细胞MDA-MB-453的生长,以及其菌落形成能力。 EA1.3A诱导对MDA-MB-453细胞的细胞凋亡,依赖于流式细胞术分析,并通过凋亡标记物切割核聚(ADP-核糖)聚合酶(CPARP)的蛋白质印迹分析验证。另外,EA1.3A诱导G0 / G1相中的细胞周期停滞。通过GC-MS的EA1.3a的化学成分显示,来自GPM的该非极性级分含有10个包含四种生物碱,三种有机酯,两个萜烯和一种儿茶酚物质的化合物,并且尚未在GPM中报道所有这些化合物。总之,通过诱导细胞凋亡和细胞周期进展的诱导癌细胞生长而抑制癌细胞生长。我们的研究揭示了新的化学基地,为GPM的抗癌活动和可行性开发来自这种广泛使用的药用植物的新抗癌剂。

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    Macau Univ Sci &

    Technol State Key Lab Qual Res Chinese Med Macau Peoples R China;

    Macau Univ Sci &

    Technol State Key Lab Qual Res Chinese Med Macau Peoples R China;

    Macau Univ Sci &

    Technol State Key Lab Qual Res Chinese Med Macau Peoples R China;

    Macau Univ Sci &

    Technol State Key Lab Qual Res Chinese Med Macau Peoples R China;

    Macau Univ Sci &

    Technol State Key Lab Qual Res Chinese Med Macau Peoples R China;

    Macau Univ Sci &

    Technol State Key Lab Qual Res Chinese Med Macau Peoples R China;

    Macau Univ Sci &

    Technol State Key Lab Qual Res Chinese Med Macau Peoples R China;

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  • 正文语种 eng
  • 中图分类 临床医学 ;
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