Takaoka Naohisa, Takayama Tatsuya, Ozono Seiichiro
Department of Urology, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu, Shizuoka, 431-3192, Japan.
Department of Urology, Jichi Medical University, 3311-1 Yakushiji, Shimotsuke, Tochigi, 329-0498, Japan.
BMC Cancer. 2017 Mar 14;17(1):192. doi: 10.1186/s12885-017-3184-x.
Renal cell carcinomas (RCCs) overexpress fatty acid binding protein 7 (FABP7). We chose to study the TUHR14TKB cell line, because it expresses higher levels of FABP7 than other cell lines derived from renal carcinomas (OS-RC-2, 786-O, 769-P, Caki-1, and ACHN).
FABP7 expression was detected using western blotting and real-time PCR. Cell proliferation was determined using an MTS assay and by directly by counting cells. The cell cycle was assayed using flow cytometry. Cell migration was assayed using wound-healing assays. An FABP7 expression vector was used to transfect RCC cell lines.
The levels of FABP7 expressed by TUHR14TKB cells and their doubling times decreased during passage. High-passage TUHR14TKB cells comprised fewer G0/G1-phase and more S-phase cells than low-passage cells. Cell proliferation differed among subclones isolated from cultures of low-passage TUHR14TKB cells. The proliferation of TUHR14TKB cells decreased when FABP7 was overexpressed, and the cell migration property of TUHR14TKB cells were decreased when FABP7 was overexpressed. High concentrations of docosatetraenoic acid and eicosapentaenoic acid accumulated in TUHR14TKB cells that overexpressed FABP7, and docosatetraenoic acid enhanced cell proliferation.
The TUHR14TKB cell line represents a heterogeneous population that does not express FABP7 when it rapidly proliferates. The differences in FABP7 function between RCC cell lines suggests that FABP7 affects cell proliferation depending on cell phenotype.
肾细胞癌(RCC)中脂肪酸结合蛋白7(FABP7)过表达。我们选择研究TUHR14TKB细胞系,因为它比其他源自肾癌的细胞系(OS-RC-2、786-O、769-P、Caki-1和ACHN)表达更高水平的FABP7。
使用蛋白质免疫印迹法和实时聚合酶链反应检测FABP7表达。使用MTS法并直接计数细胞来测定细胞增殖。使用流式细胞术分析细胞周期。使用伤口愈合试验分析细胞迁移。使用FABP7表达载体转染RCC细胞系。
TUHR14TKB细胞表达的FABP7水平及其倍增时间在传代过程中降低。高传代的TUHR14TKB细胞比低传代细胞包含更少的G0/G1期细胞和更多的S期细胞。从低传代TUHR14TKB细胞培养物中分离的亚克隆之间的细胞增殖有所不同。当FABP7过表达时,TUHR14TKB细胞的增殖降低,并且当FABP7过表达时,TUHR14TKB细胞的细胞迁移特性降低。高浓度的二十二碳四烯酸和二十碳五烯酸在过表达FABP7的TUHR14TKB细胞中积累,并且二十二碳四烯酸增强细胞增殖。
TUHR14TKB细胞系代表一个异质群体,当其快速增殖时不表达FABP7。RCC细胞系之间FABP7功能的差异表明FABP7根据细胞表型影响细胞增殖。