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7-异戊烯氧基香豆素类化合物和蛇床子素对MCF-7细胞系细胞毒性作用的比较分析

Comparative analysis of the cytotoxic effect of 7-prenyloxycoumarin compounds and herniarin on MCF-7 cell line.

作者信息

Mousavi Seyed Hadi, Davari Atiyeh-Sadat, Iranshahi Mehrdad, Sabouri-Rad Sarvenaz, Tayarani Najaran Zahra

机构信息

Medical Toxicology Research Centre, Mashhad, University of Medical Sciences, Mashhad, Iran. ; Pharmacological Research Centre of Medicinal Plants, School of Medicine, Mashhad, University of Medical Sciences, Mashhad, Iran.

Medical Toxicology Research Centre, Mashhad, University of Medical Sciences, Mashhad, Iran.

出版信息

Avicenna J Phytomed. 2015 Nov-Dec;5(6):520-30.

Abstract

OBJECTIVE

7-prenyloxycoumarins are a group of secondary metabolites that are found mainly in plants belonging to the Rutaceae and Umbelliferae families. This study was designed to evaluate and compare the cytotoxic and apoptotic activity of 7-prenyloxycoumarin compounds and herniarin on MCF-7, a breast carcinoma cell line.

MATERIALS AND METHODS

Cells were cultured in RPMI medium and incubated with different concentrations of auraptene, herniarin, umbelliferone, and umbelliprenin. Cell viability was quantified by MTT assay. Apoptotic cells were determined using propidium iodide staining of DNA fragmentation by flow cytometry (sub-G1peak). Bax protein expression was detected by western blot to investigate the underlying mechanism.

RESULTS

Doses which induced 50% cell growth inhibition (IC50) against MCF-7 cells with auraptene, herniarin, umbelliferone, and umbelliprenin were calculated (59.7, 207.6, 476.3, and 73.4 µM), respectively. Auraptene induced a sub-G1 peak in the flow cytometry histogram of treated cells compared to control cells, and DNA fragmentation suggested the induction of apoptosis. Western blot analysis showed that auraptene significantly up-regulated Bax expression in MCF-7 cells compared to untreated controls.

CONCLUSION

Auraptene exerts cytotoxic and apoptotic effects in breast carcinoma cell line and can be considered for further mechanistic evaluations in human cancer cells. These results candidate auraptene for further studies to evaluate its biosafety and anti-cancer effects.

摘要

目的

7-异戊烯氧基香豆素是一类次生代谢产物,主要存在于芸香科和伞形科植物中。本研究旨在评估并比较7-异戊烯氧基香豆素类化合物和蛇床子素对乳腺癌细胞系MCF-7的细胞毒性和凋亡活性。

材料与方法

细胞在RPMI培养基中培养,并与不同浓度的金合欢醇、蛇床子素、伞形花内酯和异戊烯基伞形花内酯孵育。通过MTT法对细胞活力进行定量。使用碘化丙啶染色通过流式细胞术(亚G1峰)测定凋亡细胞。通过蛋白质免疫印迹法检测Bax蛋白表达以研究潜在机制。

结果

计算出金合欢醇、蛇床子素、伞形花内酯和异戊烯基伞形花内酯对MCF-7细胞诱导50%细胞生长抑制(IC50)的剂量分别为(59.7、207.6、476.3和73.4 μM)。与对照细胞相比,金合欢醇在处理细胞的流式细胞术直方图中诱导了一个亚G1峰,DNA片段化表明诱导了凋亡。蛋白质免疫印迹分析表明,与未处理的对照相比,金合欢醇在MCF-7细胞中显著上调了Bax表达。

结论

金合欢醇在乳腺癌细胞系中发挥细胞毒性和凋亡作用,可考虑在人类癌细胞中进行进一步的机制评估。这些结果使金合欢醇成为进一步研究以评估其生物安全性和抗癌作用的候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11c5/4678497/bbb6279a8557/AJP-5-520-g001.jpg

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