Farooq Muhammad, Abutaha Nael, Mahboob Shahid, Baabbad Almohannad, Almoutiri Nawaf D, Wadaan Mohammad Ahmed A M
College of Science, Department of Zoology, King Saud University, 11451 Riyadh, Saudi Arabia.
Department of Zoology, College of Science, King Saud University, 11451 Riyadh, Saudi Arabia.
Saudi J Biol Sci. 2020 Feb;27(2):611-622. doi: 10.1016/j.sjbs.2019.11.042. Epub 2019 Dec 6.
Recent trends in anticancer therapy is to use therapeutic agents which not only kill the cancer cell, but are less toxic to surrounding normal cells/tissue. One approach is to cut the nutrient supply to growing tumor cells, by blocking the formation of new blood vessels around the tumor. As the phytochemicals and botanical crude extracts have proven their efficacy as natural antiangiogenic agents with minimum toxicities, there is need to explore varieties of medicinal plants for novel antiangiogenic compounds. (Humeidh), is an annual herbal plant with proven medicinal values. The antiangiogenic potential, and developmental toxicity of humeidh in experimental animal models has never been studied before. The crude extracts were prepared from the roots, stems, leaves and flowers of in methanol, chloroform, ethyl acetate and n-hexane. The developmental toxicity screening in zebrafish embryos, has revealed that was not toxic to zebrafish embryos The chloroform stem extract showed significant level of antiangiogenic activity in zebrafish angiogenic assay on a dose dependent manner. Thirty five (35) bioactive compounds were identified by gas chromatography mass spectrophotometry (GC-MS) analysis in the stem extract of . Propanoic acid, 2-[(trimethylsilyl)oxy]-, trimethylsilyl ester, Butane, 1,2,3-tris(trimethylsiloxy), and Butanedioic acid, bis(trimethylsilyl) ester were identified as major compound present in the stem of . The anticancer activity of roots, stem, leaves and flowers crude extract was evaluated in human breast cancer (MCF7), human colon carcinoma (Lovo, and Caco-2), human hepatocellular carcinoma (HepG2) cell lines. Most of the crude extracts did not show significant level of cytotoxicity in tested cancer cells line, except, chloroform extract of stem which exhibited strong anticancer activity in all tested cancer cells with IC values in micro molar range. Based on these results, it is recommended that formulation prepared from can further be tested in clinical trials in order to explore its therapeutic potential as an effective and safe natural anticancer product.
抗癌治疗的最新趋势是使用不仅能杀死癌细胞,而且对周围正常细胞/组织毒性较小的治疗药物。一种方法是通过阻断肿瘤周围新血管的形成来切断生长中的肿瘤细胞的营养供应。由于植物化学物质和植物粗提物已被证明是具有最小毒性的天然抗血管生成剂,因此有必要探索各种药用植物以寻找新型抗血管生成化合物。(胡迈德)是一种具有已证实药用价值的一年生草本植物。胡迈德在实验动物模型中的抗血管生成潜力和发育毒性此前从未被研究过。从胡迈德的根、茎、叶和花中用甲醇、氯仿、乙酸乙酯和正己烷制备粗提物。在斑马鱼胚胎中的发育毒性筛选表明,胡迈德对斑马鱼胚胎无毒。氯仿茎提取物在斑马鱼血管生成试验中呈剂量依赖性地显示出显著水平的抗血管生成活性。通过气相色谱 - 质谱联用(GC - MS)分析在胡迈德的茎提取物中鉴定出3种生物活性化合物。丙酸,2 - [(三甲基甲硅烷基)氧基] - ,三甲基甲硅烷基酯、丁烷,1,2,3 - 三(三甲基硅氧基)和丁二酸,双(三甲基甲硅烷基)酯被鉴定为胡迈德茎中存在的主要化合物。在人乳腺癌(MCF7)、人结肠癌(Lovo和Caco - 2)、人肝癌(HepG2)细胞系中评估了根、茎、叶和花粗提物的抗癌活性。除了茎的氯仿提取物在所有测试癌细胞中表现出强抗癌活性且IC值在微摩尔范围内外,大多数粗提物在测试癌细胞系中未显示出显著水平的细胞毒性。基于这些结果,建议进一步在临床试验中测试由胡迈德制备的制剂,以探索其作为有效且安全的天然抗癌产品的治疗潜力。 (注:原文中“Thirty five (35) bioactive compounds were identified by gas chromatography mass spectrophotometry (GC-MS) analysis in the stem extract of.”疑似有信息错误,根据语境推测这里应该是3种生物活性化合物,已按3种翻译)