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8-甲氧基-2,5-二甲基-5H-吲哚并[2,3-b]喹啉作为一种潜在的抗肿瘤剂通过 PI3K/AKT/mTOR 信号通路的生物学评价

Biological Evaluation of 8-Methoxy-2,5-dimethyl-5H-indolo[2,3-b] Quinoline as a Potential Antitumor Agent via PI3K/AKT/mTOR Signaling.

机构信息

School of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730000, China.

Faculty of Applied Science, Macao Polytechnic University, Macao, China.

出版信息

Int J Mol Sci. 2023 Oct 13;24(20):15142. doi: 10.3390/ijms242015142.

Abstract

Chemotherapy is commonly used clinically to treat colorectal cancer, but it is usually prone to drug resistance, so novel drugs need to be developed continuously to treat colorectal cancer. Neocryptolepine derivatives have attracted a lot of attention because of their good cytotoxic activity; however, cytotoxicity studies on colorectal cancer cells are scarce. In this study, the cytotoxicity of 8-methoxy-2,5-dimethyl-5H-indolo[2,3-b] quinoline (MMNC) in colorectal cells was evaluated. The results showed that MMNC inhibits the proliferation of HCT116 and Caco-2 cells, blocks the cell cycle in the G2/M phase, decreases the cell mitochondrial membrane potential and induces apoptosis. In addition, the results of western blot experiments suggest that MMNC exerts cytotoxicity by inhibiting the expression of PI3K/AKT/mTOR signaling pathway-related proteins. Based on these results, MMNC is a promising lead compound for anticancer activity in the treatment of human colorectal cancer.

摘要

化疗通常被临床用于治疗结直肠癌,但它通常容易产生耐药性,因此需要不断开发新的药物来治疗结直肠癌。新隐杯苋碱衍生物因其良好的细胞毒性活性而受到广泛关注;然而,对结直肠癌细胞的细胞毒性研究还很少。在这项研究中,评估了 8-甲氧基-2,5-二甲基-5H-吲哚并[2,3-b]喹啉(MMNC)在结直肠细胞中的细胞毒性。结果表明,MMNC 抑制 HCT116 和 Caco-2 细胞的增殖,将细胞周期阻滞在 G2/M 期,降低细胞线粒体膜电位并诱导细胞凋亡。此外,western blot 实验结果表明,MMNC 通过抑制 PI3K/AKT/mTOR 信号通路相关蛋白的表达发挥细胞毒性作用。基于这些结果,MMNC 是一种有前途的先导化合物,可用于治疗人类结直肠癌的抗癌活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e2/10606936/48d2eab89e61/ijms-24-15142-g001.jpg

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