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毛霉属多形孢变种微生物转化的一种新的倍半萜香豆素诱导人胃癌细胞系 MGC-803 凋亡。

A new terpene coumarin microbial transformed by Mucor polymorphosporus induces apoptosis of human gastric cancer cell line MGC-803.

机构信息

Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, 100193, People's Republic of China.

Shenzhen Luohu People's Hospital, The Third Affiliated Hospital of Shenzhen University, Shenzhen, 518035, People's Republic of China.

出版信息

Arch Pharm Res. 2018 Jun;41(6):646-654. doi: 10.1007/s12272-018-1028-0. Epub 2018 Apr 4.

Abstract

2'-Z auraptene (1) is a synthesized monoterpene coumarin with anticancer activity against human gastric cancer cells. In order to find new potential anticancer agent, Mucor polymorphosporus was used to transform cis-auraptene. Four new terpene coumarins with notable changes in the skeletal backbone, 2'-Z auraptene A-D (2-5), were obtained and evaluated for their antiproliferative effects against human normal gastric epithelium cells and human gastric cancer cells. These new compounds showed selective cytotoxic activity against MGC-803 cells with IC values from 0.78 ± 0.13 to 10.78 ± 1.83 μM and the therapeutic index could also be significantly improved (TI = 59.0) compared with that of 1 (TI = 5.5). The structures of these metabolites were elucidated through extensive spectroscopic methods, and the possible biotransformation pathway of 1 by Mucor polymorphosporus was also proposed. Furthermore, the mechanism of the antiproliferative effects against MGC-803 cells of the most potent compound, 2'-Z auraptene A (2), was characterized. Annexin V/PI staining and abnormal expression of apoptosis-related protein suggested that compound 2 induces apoptosis in gastric cancer MGC-803 cells. Therefore, it is possible that compound 2 has the potential to be applied in gastric cancer therapy.

摘要

2'-Z 奥瑞他汀(1)是一种具有抗癌活性的合成单萜香豆素,可抑制人胃癌细胞。为了寻找新的潜在抗癌药物,采用多形被孢霉转化顺式奥瑞他汀。从转化产物中分离得到四个新的骨架发生显著变化的倍半萜香豆素 2'-Z 奥瑞他汀 A-D(2-5),并对其对人正常胃上皮细胞和人胃癌细胞的增殖抑制作用进行了评价。这些新化合物对 MGC-803 细胞表现出选择性细胞毒性,IC 值为 0.78±0.13 至 10.78±1.83 μM,治疗指数(TI)也显著提高(TI=59.0),与化合物 1(TI=5.5)相比。通过广泛的光谱方法阐明了这些代谢物的结构,并提出了多形被孢霉转化 1 的可能生物转化途径。此外,还对活性最强的化合物 2'-Z 奥瑞他汀 A(2)对 MGC-803 细胞的增殖抑制作用机制进行了研究。Annexin V/PI 染色和凋亡相关蛋白的异常表达表明,化合物 2 诱导胃癌 MGC-803 细胞凋亡。因此,化合物 2 有可能应用于胃癌的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72fe/6028838/f86c2971f07b/12272_2018_1028_Fig1_HTML.jpg

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