Tan Yan, Xiang Junyu, Huang Zixian, Wang Lin, Huang Yiling
Department of Pulmonary and Critical Care Medicine, the First People's Hospital of Yunnan Province (The Affiliated Hospital of Kunming University of Science and Technology), Kunming, China.
Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges University, Yichang, China.
J Thorac Dis. 2022 Apr;14(4):1193-1202. doi: 10.21037/jtd-22-282.
A number of studies have demonstrated that trichosanthin (TCS) can induce apoptosis in numerous types of tumor cell lines. However, whether TCS can induce pyroptosis has not yet been reported. This study aimed to investigate the role of TCS and its inhibitory effect on tumor growth by modulating pyroptosis in non-small cell lung cancer (NSCLC).
Effects of different concentrations of TCS on the cell viability, proliferation, migration and invasion of NSCLC were detected by Cell Counting Kit-8 (CCK-8), colony formation, migration, and invasion assays. Immunofluorescence was used to detect the effect of TCS on the expression of pyroptosis marker protein gasdermin-D (GSDMD)-N in A549 cells. A tumor xenograft animal model was established by injecting A549 cells into nude mice.
In the present study, we found that TCS significantly inhibited the proliferation, migration, and invasion of A549 cells in a concentration-dependent manner. In addition, TCS at a high concentration (40 µg/mL) significantly promoted the expression of pyroptosis-related proteins [GSDMD-N, NLR family pyrin domain containing 3 (NLRP3), apoptosis-associated speck-like protein containing a CARD (ASC), caspase-1, and GSDMD], which showed an inhibitory effect on the pyroptosis of A549 cells. Additionally, we found that necrosulfonamide (NSA) significantly reversed the inhibitory effect of high concentrations of TCS on the pyroptosis of A549 cells. The in vivo experiments showed that TCS effectively reduced the tumor volume and inhibited the expression of Ki-67, whereas it increased the expression of GSDMD-N.
Taken together, these results indicated that TCS could inhibit the progression of NSCLC by promoting pyroptosis. These findings provide further information on the possible underlying mechanism of TCS in the treatment of NSCLC.
多项研究表明,天花粉蛋白(TCS)可诱导多种肿瘤细胞系发生凋亡。然而,TCS是否能诱导细胞焦亡尚未见报道。本研究旨在探讨TCS通过调节非小细胞肺癌(NSCLC)中的细胞焦亡对肿瘤生长的作用及其抑制效果。
采用细胞计数试剂盒-8(CCK-8)、集落形成、迁移和侵袭实验检测不同浓度TCS对NSCLC细胞活力、增殖、迁移和侵袭的影响。采用免疫荧光法检测TCS对A549细胞中细胞焦亡标志物蛋白gasdermin-D(GSDMD)-N表达的影响。通过将A549细胞注射到裸鼠体内建立肿瘤异种移植动物模型。
在本研究中,我们发现TCS以浓度依赖性方式显著抑制A549细胞的增殖、迁移和侵袭。此外,高浓度(40μg/mL)的TCS显著促进细胞焦亡相关蛋白[GSDMD-N、含NLR家族pyrin结构域3(NLRP3)、含CARD的凋亡相关斑点样蛋白(ASC)、半胱天冬酶-1和GSDMD]的表达,这对A549细胞的细胞焦亡具有抑制作用。此外,我们发现坏死磺酰胺(NSA)显著逆转了高浓度TCS对A549细胞细胞焦亡的抑制作用。体内实验表明,TCS有效减小了肿瘤体积并抑制了Ki-67的表达,而增加了GSDMD-N的表达。
综上所述,这些结果表明TCS可通过促进细胞焦亡抑制NSCLC的进展。这些发现为TCS治疗NSCLC的潜在机制提供了进一步的信息。