Wang Sumei, Peng Zhiwei, Li Wenjuan, Long Shunqin, Xiao Shujing, Wu Wanyin
Department of Oncology, Clinical and Basic Research Team of TCM Prevention and Treatment of NSCLC, Guangdong Provincial Hospital of Chinese Medicine, The Second Clinical Medical College of Guangzhou University of Chinese Medicine, No. 111, Dade Road, Guangzhou, 510120 Guangdong People's Republic of China.
The Postdoctoral Research Station, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, 510120 Guangdong People's Republic of China.
Cancer Cell Int. 2020 May 24;20:185. doi: 10.1186/s12935-020-01270-3. eCollection 2020.
Our previous clinical study has shown that Chinese herbal medicine (CHM) Fuzheng Kang-Ai (FZKA) decoction is effective in treating advanced lung cancer patients through prolonging the drug resistance to Gefitinib (GFTN). Our basic study found that FZKA decoction could enhance the inhibition effect of GFTN in lung cancer by inactivating PI3K/Akt pathway. Moreover, our recent work showed that FZKA induced lung cancer cell apoptosis via STAT3/Bcl-2/Caspase-3 pathway. Thus in this study, we aim to elucidate how FZKA enhances the effect of GFTN in lung cancer from the perspective of cell apoptosis.
Cell proliferation and colony formation assay were performed to detect the cell growth inhibition. Flow cytometry and TUNEL assay were carried out to test the cell apoptosis. Mitochondrial membrane potential (MMP) assay was done to measure the alteration of MMP. Caspase-3/-9 activity assay was used to test the activity of caspase-3/-9. Western blot and qRT-PCR were done to detect the expression of STAT3 and Bcl-2 family as well as Caspase-3/-9 and Cyt- at protein and mRNA levels, respectively. Transient transfection was performed to silence STAT3 using siSTAT3. Animal model was done to validate the molecular mechanisms in vivo and immunohistochemistry was done to detect the expression of Bax and Caspase-3.
Firstly, our results showed that FZKA enhanced the inhibition effect of GFTN in lung cancer both in vitro and in vivo. Secondly, cell apoptosis was enhanced when treating lung cancer cells with both FZKA and GFTN, a process involving the mitochondria and the Bcl-2 family. And Bcl-2 family was involved in this process. Interestingly, STAT3 plays a critical role on mediating the above process. Last but not the least, the enhanced effect of cell apoptosis induction of GFTN by FZKA was validated in animal model.
Our findings conclude that Fuzheng Kang-Ai decoction enhances the effect of GFTN-induced cell apoptosis in lung cancer through the mitochondrial pathway, providing a novel molecular mechanism by which FZKA sensitizes to GFTN by delaying drug resistance in treating lung cancer patients.
我们之前的临床研究表明,中药扶正抗癌(FZKA)汤通过延长对吉非替尼(GFTN)的耐药性,对晚期肺癌患者有效。我们的基础研究发现,FZKA汤可通过使PI3K/Akt通路失活来增强GFTN对肺癌的抑制作用。此外,我们最近的研究表明,FZKA通过STAT3/Bcl-2/Caspase-3通路诱导肺癌细胞凋亡。因此,在本研究中,我们旨在从细胞凋亡的角度阐明FZKA如何增强GFTN对肺癌的疗效。
进行细胞增殖和集落形成试验以检测细胞生长抑制。进行流式细胞术和TUNEL试验以检测细胞凋亡。进行线粒体膜电位(MMP)试验以测量MMP的变化。使用Caspase-3/-9活性试验检测Caspase-3/-9的活性。分别进行蛋白质印迹法和qRT-PCR以检测STAT3和Bcl-2家族以及Caspase-3/-9和Cyt-在蛋白质和mRNA水平的表达。使用siSTAT3进行瞬时转染以沉默STAT3。建立动物模型以在体内验证分子机制,并进行免疫组织化学检测Bax和Caspase-3的表达。
首先,我们的结果表明,FZKA在体外和体内均增强了GFTN对肺癌的抑制作用。其次,用FZKA和GFTN处理肺癌细胞时,细胞凋亡增强,这一过程涉及线粒体和Bcl-2家族。并且Bcl-2家族参与了这一过程。有趣的是,STAT3在介导上述过程中起关键作用。最后但同样重要的是,FZKA增强GFTN诱导细胞凋亡的作用在动物模型中得到了验证。
我们的研究结果表明,扶正抗癌汤通过线粒体途径增强GFTN诱导的肺癌细胞凋亡,为FZKA在治疗肺癌患者中通过延迟耐药性使对GFTN敏感提供了一种新的分子机制。