Kola P, Manjula S N, Metowogo K, Madhunapantula S V, Eklu-Gadegbeku K
Research Unit Pathophysiology-Bioactive Substances and Safety, Faculty of Sciences, University of Lome, 01 BP: 1515, Lome, Togo.
Department of Pharmacology, JSS College of Pharmacy, JSS Academy of Higher Education & Research (JSS AHER), Mysuru, 570015, India.
Heliyon. 2023 Feb 23;9(3):e13869. doi: 10.1016/j.heliyon.2023.e13869. eCollection 2023 Mar.
Cancer is leading to premature deaths across the globe. Therapeutic approaches are still being developed to enhance the survival of cancer patients. In our previous study, extracts from four Togolese plants, namely, (CP), (PT), (PP), and (SL), actually used in traditional medicine for cancer treatment, showed beneficial health effects against oxidative stress, inflammation, and angiogenesis.
In the present study, we aimed to investigate the cytotoxicity and antitumor activities of these four plant extracts.
Breast, lung, cervical, and liver cancer cell lines were exposed to the extracts, and viability was assessed using the Sulforhodamine B method. and with significant cytotoxicity were selected for tests. The acute oral toxicity of these extracts was assessed using BALB/c mice. The antitumor activity was evaluated using the EAC tumor bearing mice model, wherein mice were orally treated with extracts at different concentrations for 14 days. The standard drug was cisplatin (3.5 mg/kg, i.p), single dose.
Cytotoxicity tests revealed that SL, PP, and CP extracts have more than 50% cytotoxicity at 150 μg/mL. The acute oral toxicity of PP and SL at 2000 mg/kg did not show any toxic signs. At therapeutic doses of 100 mg/kg, 200 mg/kg and 400 mg/kg of PP and 40 mg/kg, 80 mg/kg, and 160 mg/kg of SL, extracts showed beneficial health effects by modulating several biological parameters. SL extract significantly reduced tumor volume (P < 0.001), cell viability, and normalized hematological parameters. SL also demonstrated a strong anti-inflammatory activity similar to the standard drug. The SL extract also revealed a significant increase of the life span of treated mice. PP extract reduced the tumor volume and significantly improved the values of endogenous antioxidants. Both PP and SL extracts also exerted significant anti-angiogenic potency.
The study indicated that polytherapy would be a panacea for the efficient use of medicinal plant extracts against cancer. This approach will make it possible to act simultaneously on several biological parameters. Molecular studies of both extracts targeting key cancer genes in several cancer cells are currently underway.
癌症正在导致全球范围内的过早死亡。仍在开发治疗方法以提高癌症患者的生存率。在我们之前的研究中,多哥的四种植物提取物,即[植物名称1](CP)、[植物名称2](PT)、[植物名称3](PP)和[植物名称4](SL),实际上在传统医学中用于癌症治疗,对氧化应激、炎症和血管生成显示出有益的健康影响。
在本研究中,我们旨在研究这四种植物提取物的细胞毒性和抗肿瘤活性。
将乳腺癌、肺癌、宫颈癌和肝癌细胞系暴露于提取物中,并使用磺酰罗丹明B法评估细胞活力。选择具有显著细胞毒性的提取物进行[具体实验名称]测试。使用BALB/c小鼠评估这些提取物的急性口服毒性。使用艾氏腹水癌(EAC)荷瘤小鼠模型评估抗肿瘤活性,其中小鼠口服不同浓度的提取物,持续14天。标准药物为顺铂(3.5mg/kg,腹腔注射),单剂量。
细胞毒性测试显示,SL、PP和CP提取物在150μg/mL时具有超过50%的细胞毒性。PP和SL在2000mg/kg的急性口服毒性未显示任何毒性迹象。在100mg/kg、200mg/kg和400mg/kg的PP治疗剂量以及40mg/kg、80mg/kg和160mg/kg的SL治疗剂量下,提取物通过调节多个生物学参数显示出有益的健康影响。SL提取物显著降低肿瘤体积(P<0.001)、细胞活力并使血液学参数正常化。SL还表现出与标准药物相似的强大抗炎活性。SL提取物还显示治疗小鼠的寿命显著延长。PP提取物减小了肿瘤体积并显著改善了内源性抗氧化剂的值。PP和SL提取物均具有显著的抗血管生成能力。
该研究表明,联合治疗将是有效利用药用植物提取物对抗癌症的万灵药。这种方法将有可能同时作用于多个生物学参数。目前正在对这两种提取物针对几种癌细胞中的关键癌症基因进行分子研究。