Su Wen, Wang Yu-Fan, Wang Feng, Yang Hui-Jun, Yang Hong-Yu
Dept. of Oral and Maxillofacial Surgery, Peking University Shenzhen Hospital, Shenzhen 518036,China.
Hua Xi Kou Qiang Yi Xue Za Zhi. 2019 Oct 1;37(5):509-515. doi: 10.7518/hxkq.2019.05.011.
To investigate the effect of circular RNA hsa_circ_0002203 on the malignant biological behavior of oral squamous cell carcinoma (OSCC) cell lines.
METHODS: Forty patients with oral squamous cell carcinoma were included. Real-time fluorescent polymerase chain reaction (PCR) was used to detect the expression level of circular RNA hsa_circ_ 0002203 in OSCC and corresponding adjacent tissues, OSCC cell lines, and human oral keratinocytes (HOK). SCC15 and CAL27 cells were transfected with lenti-virus. The expression level of circular RNA hsa_circ_0002203 was detected by real-time fluorescent PCR. Cell proliferation was detected by cell counting assay (CCK-8). Cell migration and invasion ability was detected by scratch assay and Transwell migration and invasion assay. Apoptosis level was detected by flow cytometry. The expression of corresponding protein was detected by Western blot. Murine tumor formation experiments were performed to observe the effect of hsa_circ_0002203 on the tumorigenesis of SCC15 cells in vivo.
RESULTS: The expression of circular RNA hsa_circ_0002203 in OSCC tissues was lower than that in adjacent tissues (P<0.01), and the expression in OSCC cell lines was lower than that in HOK (P<0.001). Hsa_circ_ 0002203 expression increased after the lentiviral infection of SCC15 and CAL27. The proliferation, migration, and invasion of SCC15 and CAL27 reduced, and apoptosis level was promoted. The tumor volume, weight decreased, and growth rate of nude mice decreased.
The low expression of circular RNA hsa_circ_0002203 in oral squamous cell carcinoma can enhance the proliferation, migration, and invasion of cancer cells and inhibit tumor cell apoptosis.
探讨环状RNA hsa_circ_0002203对口腔鳞状细胞癌(OSCC)细胞系恶性生物学行为的影响。
纳入40例口腔鳞状细胞癌患者。采用实时荧光聚合酶链反应(PCR)检测环状RNA hsa_circ_0002203在OSCC组织及其相应癌旁组织、OSCC细胞系和人正常口腔角质形成细胞(HOK)中的表达水平。用慢病毒转染SCC15和CAL27细胞。采用实时荧光PCR检测环状RNA hsa_circ_0002203的表达水平。采用细胞计数试剂盒(CCK-8)检测细胞增殖情况。采用划痕实验及Transwell迁移和侵袭实验检测细胞迁移和侵袭能力。采用流式细胞术检测细胞凋亡水平。采用蛋白质免疫印迹法检测相应蛋白的表达。进行小鼠肿瘤形成实验,观察hsa_circ_0002203对SCC15细胞体内成瘤的影响。
环状RNA hsa_circ_0002203在OSCC组织中的表达低于癌旁组织(P<0.01),在OSCC细胞系中的表达低于HOK(P<0.001)。慢病毒感染SCC15和CAL27细胞后,hsa_circ_0002203表达增加。SCC15和CAL27细胞的增殖、迁移和侵袭能力降低,细胞凋亡水平升高。裸鼠肿瘤体积、重量减小,生长速度减慢。
环状RNA hsa_circ_0002203在口腔鳞状细胞癌中低表达可增强癌细胞的增殖、迁移和侵袭能力,并抑制肿瘤细胞凋亡。