Yang Zhijing, Liu Da, Zhou Hengzong, Tao Boqiang, Chang Lu, Liu Huimin, Luo Haoming, Wang Dongxu, Liu Weiwei
Department of Oral and Maxillofacial Surgery, Hospital of Stomatology, Jilin University, Changchun, China.
Laboratory Animal Center, College of Animal Science, Jilin University, Changchun, China.
Front Bioeng Biotechnol. 2021 Nov 26;9:766380. doi: 10.3389/fbioe.2021.766380. eCollection 2021.
Although the therapeutic strategy showed significant improvement, the therapeutic effect was poor on metastases in tongue squamous cell carcinoma (TSCC) which is the most malignant tumor found in the head and neck. Chrysin, similar to the flavonoids, plays an antitumor role by regulating the expression of ncRNAs in many kinds of cancers. Compared to flavonoids, gold nanoparticles (AuNPs) provide a novel insight into inhibiting cancer cell growth via photothermal therapy (PPT) which is irradiated by near-infrared radiation (NIR). However, most flavonoids and AuNPs lack specificity of tumor . The extracellular vesicles (EVs) which were abundant with ncRNAs are isolated from the cellular supernatant fluid and have the ability to carry drugs or nanoparticles to improve specificity. In the present study, we aimed to synthesize a new nanomaterial based on EVs containing chrysin and analyzed cell apoptosis in TSCC cells. Our results demonstrated that EVs-chrysin were isolated from SCC9 cells that were treated with chrysin. To improve the therapeutic effect, AuNPs were carried by EVs-chrysin (Au-EVs). Compared to BGC823 and HCC-LM3 cells, the uptake of Au-EVs was specific in SCC9 cells. Moreover, Au-EVs combined with NIR enhanced cell apoptosis in TSCC cells. To confirm the role of miRNAs in cell apoptosis, the differentially expressed miRNAs between EVs-Con and EVs-chrysin were screened by RNA-seq. The results revealed that the let-7a-3p family, which acts as the tumor suppressor, was upregulated in EVs-chrysin compared to EVs-Con. Thus, let-7a-3p was screened in the apoptosis pathway that was associated with the p53 protein. Furthermore, compared to the Con group, Au-EVs combined with the NIR group effectively inhibited tumor growth via increasing the expression of let-7a-3p. Together, as a new nanomaterial, Au-EVs induced cell apoptosis and inhibited tumor growth by regulating let-7a-3p expression in TSCC.
尽管该治疗策略显示出显著改善,但对头颈部最恶性的肿瘤——舌鳞状细胞癌(TSCC)的转移灶治疗效果不佳。与类黄酮类似,白杨素通过调节多种癌症中ncRNAs的表达发挥抗肿瘤作用。与类黄酮相比,金纳米颗粒(AuNPs)通过近红外辐射(NIR)照射的光热疗法(PPT)为抑制癌细胞生长提供了新的见解。然而,大多数类黄酮和AuNPs缺乏肿瘤特异性。从细胞上清液中分离出富含ncRNAs的细胞外囊泡(EVs),其具有携带药物或纳米颗粒以提高特异性的能力。在本研究中,我们旨在合成一种基于含有白杨素的EVs的新型纳米材料,并分析TSCC细胞中的细胞凋亡。我们的结果表明,EVs-白杨素是从用白杨素处理的SCC9细胞中分离出来的。为了提高治疗效果,AuNPs由EVs-白杨素携带(Au-EVs)。与BGC823和HCC-LM3细胞相比,Au-EVs在SCC9细胞中的摄取具有特异性。此外,Au-EVs与NIR联合增强了TSCC细胞中的细胞凋亡。为了证实miRNAs在细胞凋亡中的作用,通过RNA测序筛选了EVs-Con和EVs-白杨素之间差异表达的miRNAs。结果显示,作为肿瘤抑制因子的let-7a-3p家族在EVs-白杨素中相对于EVs-Con上调。因此,在与p53蛋白相关的凋亡途径中筛选了let-7a-3p。此外,与对照组相比,Au-EVs联合NIR组通过增加let-7a-3p的表达有效抑制了肿瘤生长。总之,作为一种新型纳米材料,Au-EVs通过调节TSCC中let-7a-3p的表达诱导细胞凋亡并抑制肿瘤生长。