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Biological features gene expression profile and mechanisms of drug resistance of two‐ and three‐dimensional hepatocellular carcinoma cell cultures

机译:两维肝细胞癌细胞培养物的生物特征基因表达谱和耐药机制

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摘要

Hepatocellular carcinoma (HCC) is a common malignant tumor with insidious onset and rapid progression. Its treatment is often difficult owing to tumor resistance. In this study, we aimed to understand the different biological characteristics, gene expression profiles, and drug resistance mechanisms of HCC cells cultured under different conditions. A conventional adherence method and a liquid overlay technique were used to prepare two‐ and three‐dimensional cultures of Bel‐7402 and 5‐fluorouracil (5‐Fu)‐resistant Bel‐7402 (Bel‐7402/5‐Fu) cells. Morphological characteristics were assessed via microscopy, and cell cycle distribution and apoptotic rate were obtained using flow cytometry. Cell sensitivity to different concentrations of drugs was detected with 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide assays. Gene expression profiles and signal transduction pathways of Bel‐7402 and Bel‐7402/5‐Fu cells under different culture conditions were determined using gene chips. Cells in three‐dimensional culture were suspended and they grew into dense multicellular spheroid (MCS) structures, aggregating with each other. In contrast to cells in the two‐dimensional culture, cell cycle arrest was observed in MCSs. The sensitivity of Bel‐7402 cells in the two‐dimensional culture to drugs at high concentrations was significantly higher than that of cells in the three‐dimensional culture (p < .05). The apoptotic rate of Bel‐7402 and Bel‐7402/5‐Fu cells was also higher in the two‐dimensional culture (p < .05). Signal transduction pathway analysis showed that after Bel‐7402 cells acquired resistance to 5‐Fu, CCND1, MCM2, and MCM3 gene expression was upregulated in the G1 to S cell cycle control signal transduction pathway, CDKN1C and CCNG2 gene expression was downregulated, and MCM2 and MCM3 gene expression was upregulated in the DNA replication signal transduction pathway. Therefore, the liquid overlay technique is a simple, low‐cost procedure to successfully construct three‐dimensional culture models of HCC. This study provides new information and methods for exploring the molecular mechanisms of liver cancer resistance, clinical treatment, development of molecular information, and interventional prevention.
机译:肝细胞癌(HCC)是一种常见的恶性肿瘤,具有阴险发作和快速进展。由于肿瘤抗性,其治疗往往难以。在这项研究中,我们旨在了解在不同条件下培养的HCC细胞的不同生物学特征,基因表达谱和耐药机制。使用常规的粘附方法和液体覆盖技术来制备Bel-7402和5-氟尿嘧啶(5-FU)-Resistant Bel-7402(Bel-7402/5-FU)单元的三维培养物。通过显微镜评估形态学特性,使用流式细胞术获得细胞周期分布和凋亡率。用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化铵测定检测对不同浓度药物的细胞敏感性。使用基因芯片测定Bel-7402和Bel-7402/5-Fu细胞的基因表达谱和信号转导途径。悬浮三维培养物中的细胞,它们成长为致密的多细胞球体(MCS)结构,彼此聚集。与二维培养中的细胞相反,在MCSS中观察到细胞周期停留。在高浓度下对二维培养物中的Bel-7402细胞对药物的敏感性显着高于三维培养中细胞(P <.05)。二维培养的Bel-7402和Bel-7402/5-FU细胞的凋亡率也较高(P <.05)。信号转导通路分析显示,在G1至S细胞周期控制信号转导途径中升高了Bel-7402细胞,CCND1,MCM2和MCM3基因表达,下调CDKN1C和CCNG2基因表达和MCM2在DNA复制信号转导通路中上调MCM3基因表达。因此,液体覆盖技术是一种简单,低成本的过程,用于成功构建HCC的三维培养模型。本研究提供了探索肝癌抗性,临床治疗,分子信息的发展和介入预防的新信息和方法。

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