Department of Health Sciences, Biomedical Program College of Arts and Sciences, Qatar University, Doha, Qatar; Biochemistry Department, Faculty of Science, Alexandria University, Alexandria, Egypt.
Department of Chemistry & Biochemistry, Edison Biotechnology Institute, Ohio University, Athens, OH 45701, USA.
Bioorg Med Chem Lett. 2014 Feb 15;24(4):1184-7. doi: 10.1016/j.bmcl.2013.12.103. Epub 2014 Jan 6.
Lung cancer is one of the most common malignancies worldwide. In this Letter, novel MOM-ether analogs of isosteviol were designed and synthesized to be tested for anticancer activities against H1299 lung cancer cell lines. The effects of these derivatives were studied in H1299 human large cell lung carcinoma cells that are null for p53 and compared to normal counterparts NL-20 normal lung epithelial cells. The initial screening of twelve MOM-ether analogs of isosteviol derivatives on H1299 lung cancer cells by MTT assay revealed that two derivatives (an ester and a carbamate) were the most potent in reducing cell viability. The IC50 values for these derivatives were determined to be 14 and 21 μM respectively. We compared the cytotoxicity of the best derivatives in H1299 lung cancer cells and NL-20 normal lung epithelial cells. Both derivatives showed lower cytotoxic effects on NL-20 normal lung epithelial cells. Moreover, both derivatives induced apoptosis in H1299 lung cancer cells more than NL-20 normal lung epithelial cells.
肺癌是世界上最常见的恶性肿瘤之一。在这封信件中,我们设计并合成了新型 MOM-醚异甜菊醇类似物,以测试它们对 H1299 肺癌细胞系的抗癌活性。这些衍生物的作用在 p53 缺失的 H1299 人大型肺癌细胞和正常对照 NL-20 正常肺上皮细胞中进行了研究。通过 MTT 分析对 12 种 MOM-醚异甜菊醇衍生物对 H1299 肺癌细胞的初步筛选表明,两种衍生物(酯和氨基甲酸酯)在降低细胞活力方面最为有效。这些衍生物的 IC50 值分别为 14 和 21 μM。我们比较了这两种最佳衍生物在 H1299 肺癌细胞和 NL-20 正常肺上皮细胞中的细胞毒性。两种衍生物对 NL-20 正常肺上皮细胞的细胞毒性较低。此外,两种衍生物在 H1299 肺癌细胞中诱导的细胞凋亡均多于 NL-20 正常肺上皮细胞。