Department of Medical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi Province, People's Republic of China.
Pharmacol Res Perspect. 2021 Feb;9(1):e00715. doi: 10.1002/prp2.715.
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.
肝细胞癌(HCC)是一种常见的恶性肿瘤,起病隐匿,进展迅速。由于肿瘤耐药,其治疗往往较为困难。本研究旨在了解不同条件下培养的 HCC 细胞的不同生物学特性、基因表达谱和耐药机制。采用常规贴壁法和液体覆盖技术,制备 Bel-7402 细胞的二维和三维培养物以及 5-氟尿嘧啶(5-Fu)耐药 Bel-7402 细胞(Bel-7402/5-Fu)。通过显微镜评估形态特征,通过流式细胞术获得细胞周期分布和凋亡率。使用 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法检测细胞对不同浓度药物的敏感性。通过基因芯片检测不同培养条件下 Bel-7402 和 Bel-7402/5-Fu 细胞的基因表达谱和信号转导通路。三维培养的细胞悬浮并生长成密集的多细胞球体(MCS)结构,彼此聚集。与二维培养的细胞相比,MCS 中观察到细胞周期停滞。二维培养的 Bel-7402 细胞对高浓度药物的敏感性明显高于三维培养的细胞(p<0.05)。二维培养的 Bel-7402 和 Bel-7402/5-Fu 细胞的凋亡率也较高(p<0.05)。信号转导通路分析表明,Bel-7402 细胞获得 5-Fu 耐药后,G1 到 S 细胞周期控制信号转导通路中 CCND1、MCM2 和 MCM3 基因表达上调,CDKN1C 和 CCNG2 基因表达下调,DNA 复制信号转导通路中 MCM2 和 MCM3 基因表达上调。因此,液体覆盖技术是一种简单、低成本的方法,可以成功构建 HCC 的三维培养模型。本研究为探索肝癌耐药的分子机制、临床治疗、分子信息开发和介入性预防提供了新的信息和方法。