Xia Xiao-Yang, Fang Fei, Liu Yan, Che Chao, Ke Jin-Juan, Jiang Sheng-Jun
Dept. of Stomatology, Hubei Integrated Traditional Chinese and Western Medicine Hospital, Wuhan 430015, China.
Dept. of Stomatology, Wuhan University People,s Hospital, Wuhan 430060, China.
Hua Xi Kou Qiang Yi Xue Za Zhi. 2021 Apr 1;39(2):164-169. doi: 10.7518/hxkq.2021.02.006.
To investigate the expression of cyclophilin A (CyPA) in oral squamous cell carcinoma (OSCC) and explore the effect of downregulating the expression of CyPA gene on the proliferation and invasion of SCC-25 cells.
A total of 77 cases of patients with OSCC were selected. The expression levels of CyPA proteins in OSCC and adjacent normal tissues were evaluated. SCC-25 cells were cultured and divided into the CyPA interference sequence group, negative control group, and blank group. The expression levels of CyPA mRNA and protein in cells were detected by using real-time fluorescent quantitative polymerase chain reaction and Western blot, respectively. Cell proliferation was detected by using methyl thiazolyl tetrazolium and plate colony formation assays. Cell invasion was detected by using Transwell assay.
The positive expression rate of CyPA protein in OSCC tissues was 76.62%, which was higher than that in adjacent tissues (<0.05). The positive expression rate of CyPA protein in TNM stage T+T, clinical stage Ⅲ+Ⅳ, moderately or poorly differentiated lymph node metastasis was increased (<0.05). Compared with the negative control and blank groups, the CyPA interference sequence group had decreased relative expression levels of CyPA mRNA and protein (<0.05); optical density va-lues of cells at 24, 48, 72, and 96 h (<0.05); and number of cell colonies and invasive cells (<0.05).
The CyPA protein is highly expressed in OSCC tissues, and the downregulation of CyPA gene expression in SCC-25 cells can reduce cell proliferation and inhibit cell invasion.
研究亲环素A(CyPA)在口腔鳞状细胞癌(OSCC)中的表达情况,并探讨下调CyPA基因表达对SCC - 25细胞增殖和侵袭的影响。
选取77例OSCC患者。评估OSCC组织及癌旁正常组织中CyPA蛋白的表达水平。培养SCC - 25细胞,分为CyPA干扰序列组、阴性对照组和空白组。分别采用实时荧光定量聚合酶链反应和蛋白质印迹法检测细胞中CyPA mRNA和蛋白的表达水平。采用噻唑蓝和平板克隆形成实验检测细胞增殖。采用Transwell实验检测细胞侵袭。
OSCC组织中CyPA蛋白阳性表达率为76.62%,高于癌旁组织(<0.05)。在TNM分期T3 + T4、临床分期Ⅲ + Ⅳ、中低分化及有淋巴结转移的患者中,CyPA蛋白阳性表达率升高(<0.05)。与阴性对照组和空白组相比,CyPA干扰序列组中CyPA mRNA和蛋白的相对表达水平降低(<0.05);24、48、72和96 h时细胞的光密度值降低(<0.05);细胞集落数和侵袭细胞数减少(<0.05)。
CyPA蛋白在OSCC组织中高表达,下调SCC - 25细胞中CyPA基因表达可降低细胞增殖并抑制细胞侵袭。