Tomizawa Minoru, Shinozaki Fuminobu, Motoyoshi Yasufumi, Sugiyama Takao, Yamamoto Shigenori, Ishige Naoki
Department of Gastroenterology, National Hospital Organization, Shimoshizu Hospital, Yotsukaido, Chiba 284-0003, Japan.
Department of Radiology, National Hospital Organization, Shimoshizu Hospital, Yotsukaido, Chiba 284-0003, Japan.
Oncol Lett. 2017 Jul;14(1):899-902. doi: 10.3892/ol.2017.6239. Epub 2017 May 24.
Tissues surrounding hepatocellular carcinomas (HCCs) lack glucose. Hepatocyte selection medium (HSM) is deficient in glucose and is supplemented with galactose. HCC cells were cultured in HSM to investigate the stem cell markers α-fetoprotein (AFP) and cluster of differentiation 44 (CD44). HCC cells (HLF and PLC/PRF/5 cells) were cultured in HSM. Viable cell numbers were determined on days 0 and 7 following culture in HSM. RNA was isolated and subjected to reverse transcription-quantitative PCR (RT-qPCR) to analyze the mRNA expression levels of AFP and CD44. Immunostaining was performed to analyze the protein levels of AFP and CD44. The number of viable cells was significantly decreased on day 7 following culture in HSM. The expression levels of AFP and CD44 increased on day 7 as assessed using RT-qPCR. Immunostaining confirmed the results of RT-qPCR analysis. The number of viable HCC cells was decreased in HSM, whereas the expression levels of AFP and CD44 increased. Therefore, HSM is potentially useful for the enrichment of HCC cells with cancer stem cell characteristics.
肝细胞癌(HCC)周围的组织缺乏葡萄糖。肝细胞选择培养基(HSM)不含葡萄糖,并添加了半乳糖。将HCC细胞培养在HSM中,以研究干细胞标志物甲胎蛋白(AFP)和分化簇44(CD44)。将HCC细胞(HLF和PLC/PRF/5细胞)培养在HSM中。在HSM中培养0天和7天后测定活细胞数量。分离RNA并进行逆转录定量PCR(RT-qPCR),以分析AFP和CD44的mRNA表达水平。进行免疫染色以分析AFP和CD44的蛋白水平。在HSM中培养7天后,活细胞数量显著减少。使用RT-qPCR评估,AFP和CD44的表达水平在第7天增加。免疫染色证实了RT-qPCR分析的结果。在HSM中,活的HCC细胞数量减少,而AFP和CD44的表达水平增加。因此,HSM可能有助于富集具有癌症干细胞特征的HCC细胞。