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紫苏醇及其生物转化代谢产物对A549和HepG2癌细胞系的细胞毒性、抗增殖和凋亡作用。

Cytotoxic, Antiproliferative and Apoptotic Effects of Perillyl Alcohol and Its Biotransformation Metabolite on A549 and HepG2 Cancer Cell Lines.

作者信息

Oturanel Ceren E, Kıran İsmail, Özşen Özge, Çiftçi Gülşen A, Atlı Özlem

机构信息

Department of Chemistry, Faculty of Science and Letters, Eskisehir Osmangazi University, 26480 Eskisehir. Turkey.

Department of Biochemistry, Faculty of Pharmacy, Anadolu University, 26470 Eskisehir. Turkey.

出版信息

Anticancer Agents Med Chem. 2017;17(9):1243-1250. doi: 10.2174/1871520617666170103093923.

Abstract

BACKGROUND

A monoterpene, perillyl alcohol, has attracted attention in medicinal chemistry since it exhibited chemo-preventive and therapeutic properties against a variety of cancers.

OBJECTIVE

In the present work, it was aimed to obtain derivatives of perillyl alcohol through microbial biotransformation and investigate their anticancer activities against A549 and HepG2 cancer cell lines.

METHOD

Biotransformation studies were carried out in a α-medium for 7 days at 25oC. XTT assay was performed to investigate the anticancer activities of perillyl alcohol and its biotransformation metabolite, dehydroperillic acid, against A549 and HepG2 cell lines and their selectivity using healthy cell line, NIH/3T3. Cell proliferation ELISA, BRDU (colorimetric) assay was used for measurement of proliferation in replicative cells in which DNA synthesis occurs. Flow cytometric analyses were also carried out for measuring apoptotic cell percentages, caspase 3 activation and mitochondrial membrane potential.

RESULTS

Biotransformation of perillyl alcohol with Fusarium culmorum yielded dehydroperillic acid in a yield of 20.4 %. In in vitro anticancer studies, perillyl alcohol was found to exert cytotoxicity against HepG2 cell line with an IC50 value of 409.2 μg/mL. However, this effect was not found to be selective because of its higher IC50 (250 μg/mL) value against NIH/3T3 cell line. On the other hand, dehydroperillic acid was found to be effective and also selective against A549 cell line with an IC50 value of 125 μg/mL and a selectivity index (SI) value of 400. Apoptosis inducing effects of dehydroperillic acid was better in A549 cell line.

CONCLUSION

Dehydroperillic acid may be a good candidate for therapy of lung adenocarcinoma and may show this anticancer activity by inducing apoptosis.

摘要

背景

单萜紫苏醇自展现出对多种癌症的化学预防和治疗特性以来,在药物化学领域引起了关注。

目的

在本研究中,旨在通过微生物生物转化获得紫苏醇的衍生物,并研究它们对A549和HepG2癌细胞系的抗癌活性。

方法

在α培养基中于25℃进行7天的生物转化研究。采用XTT法研究紫苏醇及其生物转化代谢产物脱氢紫苏酸对A549和HepG2细胞系的抗癌活性以及使用健康细胞系NIH/3T3的选择性。细胞增殖ELISA、BRDU(比色)测定法用于测量发生DNA合成的复制细胞中的增殖情况。还进行了流式细胞术分析以测量凋亡细胞百分比、半胱天冬酶3激活和线粒体膜电位。

结果

用禾谷镰刀菌对紫苏醇进行生物转化,脱氢紫苏酸的产率为20.4%。在体外抗癌研究中,发现紫苏醇对HepG2细胞系具有细胞毒性,IC50值为409.2μg/mL。然而,由于其对NIH/3T3细胞系的IC50值较高(250μg/mL),这种作用没有选择性。另一方面,发现脱氢紫苏酸对A549细胞系有效且具有选择性,IC50值为125μg/mL,选择性指数(SI)值为400。脱氢紫苏酸在A549细胞系中的凋亡诱导作用更好。

结论

脱氢紫苏酸可能是肺腺癌治疗的良好候选药物,并且可能通过诱导凋亡显示这种抗癌活性。

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