Akamse Muriel Angounou, Kamgo Vigny Diembo, Ango Patrick Yves, Fotsing Marthe Carine Djuidje, Fomat Boris Hugor Pehuie, Mmutlane Edwin, Fotso Ghislain Wabo, Kapche Deccaux Wabo Fotso Gilbert, Zingué Stephane, Ndinteh Derek Tantoh
Department of Organic Chemistry, Faculty of Science, University of Yaoundé 1, Yaoundé, Cameroon.
Department of Pharmacotoxicology and Pharmacokinetics, Faculty of Medicine and Biomedical Sciences, University of Yaoundé 1, Yaoundé, Cameroon.
Cancer Rep (Hoboken). 2025 Sep;8(9):e70337. doi: 10.1002/cnr2.70337.
Breast cancer is a major public health issue. In 2022, approximately 4,207 new cases and 2,285 deaths were reported in Cameroon. Given the limited accessibility and various issues associated with conventional treatments, herbal medicine has emerged as a promising alternative.
This study aimed to evaluate the potential anticancer activity of naturally occurring compounds isolated from Terminalia ivorensis A. Chev.
This was done by fractionating the methanolic extract of T. ivorensis and purifying the constituents obtained using conventional chromatographic techniques. Thereafter, the crude extract and its 5 isolates were subjected to in vitro MTT bioassay to assess their potential to kill human (MCF-7 and MDA-MB-231) and murine (4T1) breast cancer cell lines. Furthermore, the potential of the most active compound (arjunolic acid) to mitigate DMBA-induced breast cancer in rats was tested. Treatments were administered for a period of 121 days; the group of rats treated with arjunolic acid (1 mg/kg) was compared to the group that received tamoxifen at 3.3 mg/kg (standard), as well as to the normal and negative control groups. Key parameters assessed included survival, tumor burden, cytokine profiles, as well as hematological, hepatic, and renal functions. Out of the 5 isolates [lupeol (1), betulinic acid (2), Arjunolic acid (3), 3,3'-Di-O-methylellagic acid-4'-O-β-D-glucopyranoside (4) 3,3',4'-Tri-O-methylellagic acid-4-O-β-Dglucopyranoside (5)] from T. ivorensis, compound (3) had the most significant inhibitory effect against breast cancer cells growth with an average CC50 of 20 μg/mL. In vivo, a significant reduction (~89%) in tumor burden and favorable modulation of inflammation, characterized by a decrease in pro-inflammatory cytokines (TNF-α, IFN-γ, IL-6, VEGF) and an increase in anti-inflammatory IL-10 was observed. Moreover, treatment with arjunolic acid led to improved survival and maintenance of body weight, without inducing any notable adverse effects.
Arjunolic acid should receive more attention as a candidate for an effective therapeutic option, combining anticancer effects with beneficial anti-inflammatory activity. We encourage further studies on this compound to better understand its mode and mechanism of action.
乳腺癌是一个重大的公共卫生问题。2022年,喀麦隆报告了约4207例新发病例和2285例死亡病例。鉴于传统治疗方法的可及性有限且存在各种问题,草药已成为一种有前景的替代方法。
本研究旨在评估从象牙楝(Terminalia ivorensis A. Chev.)中分离出的天然化合物的潜在抗癌活性。
通过将象牙楝的甲醇提取物进行分馏,并使用传统色谱技术纯化所得成分来实现这一目的。此后,对粗提物及其5种分离物进行体外MTT生物测定,以评估它们杀死人(MCF-7和MDA-MB-231)和小鼠(4T1)乳腺癌细胞系的潜力。此外,还测试了最具活性的化合物(阿朱诺酸)减轻二甲基苯并蒽(DMBA)诱导的大鼠乳腺癌的潜力。治疗持续121天;将用阿朱诺酸(1毫克/千克)治疗的大鼠组与接受3.3毫克/千克他莫昔芬(标准)治疗的组以及正常对照组和阴性对照组进行比较。评估的关键参数包括生存率、肿瘤负荷、细胞因子谱以及血液学、肝脏和肾脏功能。从象牙楝的5种分离物[羽扇豆醇(1)、桦木酸(2)、阿朱诺酸(3)、3,3'-二-O-甲基鞣花酸-4'-O-β-D-吡喃葡萄糖苷(4)、3,3',4'-三-O-甲基鞣花酸-4-O-β-D-吡喃葡萄糖苷(5)]中,化合物(3)对乳腺癌细胞生长的抑制作用最为显著,平均半数细胞毒性浓度(CC50)为20微克/毫升。在体内,观察到肿瘤负荷显著降低(约89%),炎症得到有利调节,表现为促炎细胞因子(肿瘤坏死因子-α、干扰素-γ、白细胞介素-6、血管内皮生长因子)减少,抗炎性白细胞介素-10增加。此外,用阿朱诺酸治疗可提高生存率并维持体重,且未引起任何明显的不良反应。
阿朱诺酸作为一种有效的治疗选择候选物,兼具抗癌作用和有益的抗炎活性,应受到更多关注。我们鼓励对该化合物进行进一步研究,以更好地了解其作用方式和机制。