Sohn Eun Jung, Won Gunho, Lee Jihyun, Yoon Sang Wook, Lee Ilho, Kim Hee Jeong, Kim Sung-Hoon
College of Korean Medicine, Kyung Hee University, Seoul, 130-701, Republic of Korea.
Int J Biol Sci. 2016 Oct 18;12(11):1279-1288. doi: 10.7150/ijbs.13453. eCollection 2016.
Malignant pleural mesothelioma (MPN), which is caused by asbestos exposure, is one of aggressive lung tumors. In the present study, we elucidated the anti-tumor mechanism of ursolic acid in malignant mesotheliomas. Ursolic acid significantly exerted cytotoxicity in a time and dose dependent manner in H28, H2452 and MSTO-211H mesothelioma cells and inhibited cell proliferation by colony formation assay in a dose-dependent fashion. Also, ursolic acid treatment accumulated the sub-G1 population, attenuated the expression of procapase 9, cyclin D1, pAKT, p-glycogen synthase kinase 3-alpha/beta (pGSK3α/β), β-catenin and nuclear factor kappa-light-chain-enhancer of activated B cells (NFkB) and also cleaved caspase 3 and poly (ADP-ribose) polymerase (PARP) in mesothelioma cells. Furthermore, ursolic acid treatment blocked epithelial and mesenchymal transition (EMT) molecules by activating E-cadherin as an epithelial marker and attenuating Vimentin, and Twist as mesenchymal molecules. Interestingly, miRNA array revealed that 23 miRNAs (>2 folds) including let-7b and miRNA3613-5p, miRNA134 and miRNA196b were significantly upregulated while 33 miRNAs were downregulated in ursolic acid treated H2452 cells. Furthermore, overexpression of let 7b using let-7b mimics enhanced the antitumor effect of ursolic acid to attenuate the expression of procaspases 3, pro-PARP, pAKT, β-catenin and Twist and increase sub-G1 accumulation in H2452 mesothelioma cells. Overall, our findings suggest that ursolic acid induces apoptosis via inhibition of EMT and activation of let7b in mesothelioma cells as a potent chemotherapeutic agent for treatment of malignant mesotheliomas.
恶性胸膜间皮瘤(MPN)是一种侵袭性肺部肿瘤,由接触石棉引起。在本研究中,我们阐明了熊果酸在恶性间皮瘤中的抗肿瘤机制。熊果酸在H28、H2452和MSTO-211H间皮瘤细胞中以时间和剂量依赖性方式显著发挥细胞毒性,并通过集落形成试验以剂量依赖性方式抑制细胞增殖。此外,熊果酸处理使亚G1期细胞群体积聚,减弱了原半胱天冬酶9、细胞周期蛋白D1、磷酸化AKT(pAKT)、磷酸化糖原合成酶激酶3α/β(pGSK3α/β)、β-连环蛋白和活化B细胞核因子κB(NFκB)的表达,还在间皮瘤细胞中切割了半胱天冬酶3和聚(ADP-核糖)聚合酶(PARP)。此外,熊果酸处理通过激活作为上皮标志物的E-钙黏蛋白并减弱波形蛋白和Twist(作为间充质分子)来阻断上皮-间质转化(EMT)分子。有趣的是,miRNA芯片显示,在熊果酸处理的H2452细胞中,包括let-7b、miRNA3613-5p、miRNA134和miRNA196b在内的23种miRNA(>2倍)显著上调,而33种miRNA下调。此外,使用let-7b模拟物过表达let 7b增强了熊果酸的抗肿瘤作用,以减弱H2452间皮瘤细胞中原半胱天冬酶3、原PARP、pAKT、β-连环蛋白和Twist的表达,并增加亚G1期积聚。总体而言,我们的研究结果表明,熊果酸作为一种治疗恶性间皮瘤的有效化疗药物,通过抑制EMT和激活let7b在间皮瘤细胞中诱导凋亡。