对沙特药用植物中可能具有眼部作用的植物成分进行体外细胞毒性研究

IF 2.9 3区 医学 Q2 INTEGRATIVE & COMPLEMENTARY MEDICINE
Ali Hendi Alghamdi, Aimun A E Ahmed, Haidar Abdalgadir, Mahadi Bashir, Asaad Khalid, Ashraf N Abdalla, Mohamed E Elzubier, Riyad Adnan Almaimani, Bassem Refaat, Khalid Alzahrani, Saleh M S Alghamdi, Sheraz Gul
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引用次数: 0

摘要

背景:转移性继发性眼部肿瘤是从包括乳腺癌在内的全身性恶性肿瘤扩散而来的。本研究旨在评估原产于沙特阿拉伯的 5 种药用植物提取物的细胞毒性:方法:为了进行初步的活性筛选,使用 MTT 试验和选择性指数测定药用植物提取物对各种癌细胞系的细胞毒性。对最有希望的提取物进行 GC-MS 分析,以确定其植物化学成分。使用最有前景的提取物进行了克隆生成试验,以确认初步结果。最后,利用 Western 印迹分析确定人乳腺腺癌(MCF7)细胞系中存活素和 P27 抑制基因的表达变化,以了解活性植物提取物的潜在机理特性:结果:5 种植物提取物的 IC50 值显示了不同的细胞毒性活性水平。与正常人胎肺成纤维细胞(MRC5)相比,Capparis spinosa L. 的叶子(BEP-07 提取物)对 MCF7 乳腺癌细胞系的活性最高(IC50 = 3.61 ± 0.99 μg/ml),选择性指数为 1.17。BEP-07 提取物对 MCF7 菌落有剂量依赖性克隆生成作用,与多柔比星的作用相当。与对照组 GAPDH 相比,BEP-07 提取物在最高剂量(14 µg/ml)时可显著降低存活素的表达,增加 P27 的表达。Capparis spinosa L.(BEP-07 提取物)的气相色谱-质谱(GC-MS)色谱图显示存在 145 种化合物,属于植物成分的不同类别。脂肪酸及其衍生物占 15.4%,而十八酸、2,3-二羟基丙酯是检测到的主要成分(7.9%):Capparis spinosa L.叶(BEP-07 提取物)具有显著的细胞毒性作用,尤其是对乳腺癌细胞。它是通过抑制存活素和上调 P27 来发挥这种作用的。在该植物提取物中检测到的植物成分可能参与了测试的细胞毒性活性,但还需要进一步的研究来完善候选药物的资料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In-vitro Cytotoxicity Investigations for Phytoconstituents of Saudi Medicinal Plants With Putative Ocular Effects.

Background: Metastatic secondary ocular tumors spread from systemic malignancies, including breast cancer. This study aimed to evaluate the cytotoxicity of extracts from 5 medicinal plants native to Saudi Arabia.

Methods: For preliminary activity screening, cytotoxicity using the MTT assay and selectivity index determinations were made for medicinal plant extracts against various cancer cell-lines. The most promising extract was subjected to GC-MS analysis to determine the phytochemical composition. Clonogenic assays were performed using the most promising extract to confirm the initial results. Finally, western blot analysis was used to determine the modulation in expression of survivin and P27 suppressor genes in the human breast adenocarcinoma (MCF7) cell-line to understand the potential mechanistic properties of the active plant extract.

Results: The 5 plant extracts showed various cytotoxic activity levels using IC50. The most active extract was found to be the leaves of Capparis spinosa L. (BEP-07 extract) against the MCF7 breast cancer cell-line (IC50 = 3.61 ± 0.99 μg/ml) and selectivity index of 1.17 compared to the normal human fetal lung fibroblast (MRC5) cells. BEP-07 extract showed a dose dependent clonogenic effect against the MCF7 colonies which was comparable with the effect of doxorubicin. BEP-07 extract caused a significant decrease of survivin and increase in P27 expression compared to control GAPDH at its highest dose (14 µg/ml). The GC-MS chromatogram of Capparis spinosa L. (BEP-07 extract) revealed the existence of 145 compounds, belonging to the diverse classes of phytoconstituents. Fatty acids and their derivatives represent 15.4%, whilst octadecanoic acid, 2,3-dihydroxypropyl ester was the principal component (7.9%) detected.

Conclusion: Leaves of Capparis spinosa L. (BEP-07 extract) exhibited a significant cytotoxic effect particularly against breast cancer cells. It exhibited this effect through survivin inhibition and via P27 upregulation. The detected phytoconstituents in the plant extract might be involved in tested cytotoxic activity, while further investigations are required to complete the drug candidate profile.

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来源期刊
Integrative Cancer Therapies
Integrative Cancer Therapies 医学-全科医学与补充医学
CiteScore
4.80
自引率
3.40%
发文量
78
审稿时长
>12 weeks
期刊介绍: ICT is the first journal to spearhead and focus on a new and growing movement in cancer treatment. The journal emphasizes scientific understanding of alternative medicine and traditional medicine therapies, and their responsible integration with conventional health care. Integrative care includes therapeutic interventions in diet, lifestyle, exercise, stress care, and nutritional supplements, as well as experimental vaccines, chrono-chemotherapy, and other advanced treatments. Contributors are leading oncologists, researchers, nurses, and health-care professionals.
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