对乳腺癌HCC70细胞的选择性细胞毒活性研究

IF 3 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Jane Busisiwe Ncongwane, Vuyelwa Jacqueline Tembu, Comfort Mduduzi Nkambule, Douglas Kemboi, Gerda Fouche, Nyeleti Vukea, Jo-Anne de la Mare
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引用次数: 0

摘要

背景:三阴性乳腺癌(TNBC)是一种侵袭性乳腺癌亚型,治疗选择有限。枸杞子是一种灌木,在传统医学中被广泛用于缓解癌症相关症状。为了从药用植物中寻找安全有效的治疗药物,本文研究了益母草(Leonotis ocymifolia)对TNBC具有抗癌活性的化合物。方法:利用IR、1D、2D NMR和MS等光谱数据对羊绒花化合物进行表征,并评估其对三阴性乳腺癌(HCC70)、激素受体阳性乳腺癌(MCF-7)和非致瘤性乳腺上皮细胞系(MCF-12A)的细胞毒活性。结果:从Leonotis属植物中分离到一种未见报道的双螺丹13S-nepetaefolin(1)和五种已知的双螺丹二萜类化合物nepetaefolin(2)、dubiin(3)、nepetaefuran(4)、leonotin(5)和leonotinin(6)。总体而言,labdane二萜对三阴性乳腺癌细胞(HCC70)具有选择性活性。其中,13S-nepetaefolin对HCC70细胞的细胞毒活性最强,IC50为24.65µM (SI = 1.08);然而,它对非致瘤性MCF-12A乳腺细胞具有同样的细胞毒性(IC50为26.55µM),而其同分异构体(2)则没有活性。这表明立体化学可能对双螺旋藻丹二萜的细胞毒活性有影响。所有化合物(1-6)均表现出吸附、分布、代谢和排泄特性(ADME),而leonotin(5)和leonotinin(6)表现出类似铅的特性和较高的合成可及性得分。结论:本研究的发现为进一步研究L. cyymifolia作为潜在的三阴性乳腺癌(TNBC)治疗药物提供了依据,包括潜在的双螺旋内酯二萜的化学衍生化(1),以提高对TNBC的选择性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Labdane Diterpenoids from Leonotis ocymifolia with Selective Cytotoxic Activity Against HCC70 Breast Cancer Cell Line.

Background: Triple-negative breast cancer (TNBC) is an aggressive subtype of breast cancer with limited therapeutic options. Leonotis ocymifolia is a shrub widely used in traditional medicine to alleviate cancer-related symptoms. In a search to find safe and efficacious therapeutic agents from medicinal plants, Leonotis ocymifolia was studied to find compounds with anticancer activity against TNBC.

Methods: Compounds from Leonotis ocymifolia were characterized using spectroscopic data such as IR, 1D and 2D NMR, and MS spectrometry and evaluated for cytotoxic activity against triple-negative breast cancer (HCC70), hormone receptor-positive breast cancer (MCF-7), and non-tumorigenic mammary epithelial cell lines (MCF-12A).

Results: A previously unreported bis-spirolabdane, 13S-nepetaefolin (1), together with five known labdane diterpenoids, namely nepetaefolin (2), dubiin (3), nepetaefuran (4), leonotin (5), and leonotinin (6), from the genus Leonotis were isolated. Overall, the labdane diterpenoids showed selective activity toward triple-negative breast cancer cells (HCC70). Of the compounds extracted, 13S-nepetaefolin demonstrated the greatest cytotoxic activity with an IC50 of 24.65 µM (SI = 1.08) against HCC70 cells; however, it was equally cytotoxic to non-tumorigenic MCF-12A breast cells (IC50 of 26.55 µM), whereas its isomer (2) showed no activity. This suggests that stereochemistry might have an effect on the cytotoxic activity of the bis-spirolabdane diterpenoids. All the compounds (1-6) demonstrated adsorption, distribution, metabolism, and excretion properties (ADME), while leonotin (5) and leonotinin (6) exhibited lead-like properties and high synthetic accessibility scores.

Conclusions: The findings from this study warrant further investigation of L. ocymifolia for potential triple-negative breast cancer (TNBC) therapeutic agents, including potential chemical derivatization of bis-spiro labdane diterpenoid (1) to improve selectivity to TNBC over non-cancer cells.

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