鸢尾蒿属植物Arjunolic Acid具有体内外抗乳腺癌作用

IF 1.9 Q4 ONCOLOGY
Cancer reports Pub Date : 2025-09-04 DOI:10.1002/cnr2.70337
Muriel Angounou Akamse, Vigny Diembo Kamgo, Patrick Yves Ango, Marthe Carine Djuidje Fotsing, Boris Hugor Pehuie Fomat, Edwin Mmutlane, Ghislain Wabo Fotso, Deccaux Wabo Fotso Gilbert Kapche, Stephane Zingué, Derek Tantoh Ndinteh
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引用次数: 0

摘要

乳腺癌是一个重大的公共卫生问题。2022年,喀麦隆报告了大约4 207例新病例和2 285例死亡。鉴于有限的可及性和与传统治疗相关的各种问题,草药已成为一种有希望的替代方案。目的:研究鸢尾草天然化合物的潜在抗癌活性。方法与结果采用常规色谱技术,对白毛犀醇提物进行分离纯化。然后,对粗提物及其5个分离物进行体外MTT生物测定,以评估其对人(MCF-7和MDA-MB-231)和小鼠(4T1)乳腺癌细胞株的杀伤能力。此外,还测试了最有效的化合物(arjunolic acid)减轻dba诱导的大鼠乳腺癌的潜力。治疗持续121天;将arjunolic acid (1 mg/kg)给药组与他莫昔芬3.3 mg/kg(标准)给药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、肿瘤负荷、细胞因子谱以及血液学、肝脏和肾脏功能。5个分离物[鹿皮醇(1)、白桦酸(2)、Arjunolic酸(3)、3,3′-二-O-甲基鞣花酸-4′-O-β- d-葡萄糖吡喃苷(4)3,3′,4′-三-O-甲基鞣花酸-4-O-β-二葡萄糖吡喃苷(5)]中,化合物(3)对乳腺癌细胞生长的抑制作用最显著,平均CC50为20 μg/mL。在体内,观察到肿瘤负荷显著减少(约89%)和炎症的有利调节,其特征是促炎细胞因子(TNF-α, IFN-γ, IL-6, VEGF)的减少和抗炎IL-10的增加。此外,用arjunolic酸治疗可以改善生存和维持体重,没有引起任何明显的不良反应。结论Arjunolic acid是一种结合抗癌和抗炎作用的有效治疗方案,值得关注。我们鼓励对该化合物的进一步研究,以更好地了解其作用方式和机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Arjunolic Acid From Terminalia ivorensis A. Chev (Combretaceae) Possesses Anti-Breast Cancer Effects In Vitro and In Vivo

Arjunolic Acid From Terminalia ivorensis A. Chev (Combretaceae) Possesses Anti-Breast Cancer Effects In Vitro and In Vivo

Background

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. Aims: This study aimed to evaluate the potential anticancer activity of naturally occurring compounds isolated from Terminalia ivorensis A. Chev.

Methods and Results

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.

Conclusion

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.

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来源期刊
Cancer reports
Cancer reports Medicine-Oncology
CiteScore
2.70
自引率
5.90%
发文量
160
审稿时长
17 weeks
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