Egbuna Chukwuebuka, Patrick-Iwuanyanwu Kingsley C, Onyeike Eugene N, Khan Johra, AlDosari Sahar, Jahan Sadaf, Adedokun Kamoru A, Imodoye Sikiru O, Bello Ibrahim O, Uche Chukwuemelie Z, Noreen Sana, Ifemeje Jonathan C
African Centre of Excellence in Public Health and Toxicological Research (ACE-PUTOR), University of Port-Harcourt, Port Harcourt, Rivers, Nigeria.
Department of Biochemistry, Faculty of Science, University of Port Harcourt, Port Harcourt, Rivers, Nigeria.
Front Chem. 2025 Feb 13;13:1487887. doi: 10.3389/fchem.2025.1487887. eCollection 2025.
Cancer is a complex global health challenge that requires novel and holistic approaches to treatment and prevention. Polyherbal medicines, composed of multiple plants with historical use in traditional medicine, have gained popularity due to their safety, cost-effectiveness, and accessibility. However, selecting the right plants and determining optimal combinations for enhanced biological effects remains challenging. To address this, a molecular docking study was conducted, targeting proteins implicated in cancer pathogenesis. The study identified bioactive compounds with strong binding energies, guiding the selection of polyherbal formulations for further experimentation. Using response surface methodology, various combinations of plant extracts were screened for their antioxidant properties and phytochemical content. Among the formulations tested, PHEE (Polyherbal Ethanolic Extract), comprising 70% soursop leaf, 5% jackfruit leaf, 5% orange peel, 15% citrus juice, and 5% apple fruit ethanolic extracts, exhibited the most potent biological activities, followed by SLEE (Soursop Leaf Ethanolic Extract), a 100% soursop leaf ethanolic extract. Design Expert Software predicted soursop leaf extract as a key contributor to desirable outcomes, attributed to its rich phytochemical composition. Cell-based assays revealed varying cytotoxic effects of the extracts on leukemia cells, with PHEE showing the highest potency (IC50 = 2.50 μg/mL), followed closely by SLEE (IC50 = 2.90 μg/mL). These effects are potentially due to the abundant acetogenins and flavonoids present in the extracts. However, caution is warranted regarding their cytotoxicity to normal cells. Apoptotic studies confirmed the ability of both PHEE and SLEE to induce programmed cell death, further supporting their potential as anticancer agents. This research underscores the importance of strategic plant combinations in polyherbal formulations and highlights PHEE as a promising candidate for further investigation in cancer treatment.
癌症是一项复杂的全球健康挑战,需要新颖且全面的治疗和预防方法。由多种在传统医学中有使用历史的植物组成的多草药药物,因其安全性、成本效益和可及性而受到欢迎。然而,选择合适的植物并确定能增强生物学效应的最佳组合仍然具有挑战性。为解决这一问题,开展了一项分子对接研究,以参与癌症发病机制的蛋白质为靶点。该研究鉴定出具有强结合能的生物活性化合物,为进一步实验选择多草药配方提供了指导。使用响应面法,筛选了植物提取物的各种组合的抗氧化特性和植物化学成分。在所测试的配方中,由70%刺果番荔枝叶、5%波罗蜜叶、5%橙皮、15%柑橘汁和5%苹果果实乙醇提取物组成的PHEE(多草药乙醇提取物)表现出最强的生物活性,其次是100%刺果番荔枝叶乙醇提取物SLEE(刺果番荔枝叶乙醇提取物)。Design Expert软件预测刺果番荔枝叶提取物是产生理想结果的关键因素,这归因于其丰富的植物化学成分。基于细胞的实验揭示了提取物对白血病细胞的不同细胞毒性作用,PHEE的效力最高(IC50 = 2.50μg/mL),紧随其后的是SLEE(IC50 = 2.90μg/mL)。这些作用可能是由于提取物中存在丰富的番荔枝内酯和黄酮类化合物。然而,对于它们对正常细胞的细胞毒性需谨慎对待。凋亡研究证实了PHEE和SLEE诱导程序性细胞死亡的能力,进一步支持了它们作为抗癌剂的潜力。这项研究强调了多草药配方中策略性植物组合的重要性,并突出了PHEE作为癌症治疗进一步研究的有前景候选物。