School of Life Sciences, Hebei University, Baoding 071002, Hebei, China; Postdoctoral Research Station of Biology, Hebei University, Baoding 071002, Hebei, China.
School of Life Sciences, Hebei University, Baoding 071002, Hebei, China.
Biomed Pharmacother. 2022 Sep;153:113392. doi: 10.1016/j.biopha.2022.113392. Epub 2022 Jul 11.
Chemotherapy is one of the main methods for malignant lung cancer treatment. However, the side effects of chemotherapy drugs are serious and it is prone to drug resistance. Therefore, multi-drug combination chemotherapy is popular in lung cancer treatment. This study found that tracheloside (TCS) was a novel inhibitor of TMEM16A which was specific high expressed in lung cancer tissues. TCS concentration dependently inhibited TMEM16A with an IC of 3.09 ± 0.21 μM. It inhibited lung cancer cells proliferation, migration, and induced cells apoptosis targeting TMEM16A. In addition, molecular docking combined with site-directed mutagenesis confirmed that the binding sites of TCS to TMEM16A were S387, E623, E624. Subsequently, multi-target combined drug administration was conducted based on the different drug targets of TCS and doxorubicin (DOX). Both in vitro and in vivo experiments indicated that the combined administration of low concentration of TCS and DOX achieved satisfactory anticancer effect, and it offset the side effects caused by high concentration of DOX. Therefore, TCS is a safe and efficient anticancer lead compound which can enhance the effect of DOX.
化疗是治疗恶性肺癌的主要方法之一。然而,化疗药物的副作用严重,且容易产生耐药性。因此,多药联合化疗在肺癌治疗中较为流行。本研究发现,獐牙菜苦苷(TCS)是一种新型的 TMEM16A 抑制剂,在肺癌组织中特异性高表达。TCS 浓度依赖性抑制 TMEM16A,其 IC 为 3.09±0.21μM。它通过靶向 TMEM16A 抑制肺癌细胞增殖、迁移,并诱导细胞凋亡。此外,分子对接结合定点突变证实 TCS 与 TMEM16A 的结合位点为 S387、E623、E624。随后,基于 TCS 和多柔比星(DOX)的不同药物靶点进行了多靶点联合药物给药。体外和体内实验均表明,低浓度 TCS 和 DOX 的联合给药达到了令人满意的抗癌效果,并且抵消了高浓度 DOX 引起的副作用。因此,TCS 是一种安全有效的抗癌先导化合物,可增强 DOX 的疗效。