The regulating role of miR-494 on HCCR1 in cervical cancer cells.

Ziwen Zheng, Xiaorong Yang, Qinde Yu, Ling Li, Li Qiao
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引用次数: 1

Abstract

This study focused on miR-494 inhibiting the proliferation, migration and invasion of cervical cancer cells by regulating HCCR1. During the study, 30 pairs of primary cervical cancer tissues and adjacent tissues diagnosed by pathology were collected, and then placed in a cryopreservation tube, immediately placed in liquid nitrogen to freeze, and then moved to a -80 °C refrigerator for storage until use. They were dipped with crystal violet staining solution for 20 minutes, washed 3 times with PBS, and dried at room temperature. The polycarbonate film on the chamber was gently cut, placed on a glass slide, and covered with neutral resin. The number of cells in 5 random fields was counted under a microscope, and the differences between the groups were compared. The qRT-PCR results showed that compared with the normal cervical tissue cell line HCCR1, the expression levels of miR-494 in cervical cancer cell lines HCCR1 and C-33A were significantly reduced. Compared with the transfection of mimics NC, the level of HCCR1mRNA and protein decreased significantly when transfected with miRNA-494mimics (P <0.05); compared with the transfection of inhibitor NC, the level of HCCR1 mRNA and protein increased significantly when transfected with miRNA-494 inhibitor (P <0.05).

miR-494在宫颈癌细胞中对HCCR1的调控作用
本研究关注miR-494通过调控HCCR1抑制宫颈癌细胞的增殖、迁移和侵袭。研究过程中,收集经病理诊断的原发性宫颈癌组织及癌旁组织30对,置于低温保存管中,立即置于液氮中冷冻,移至-80℃冰箱保存备用。用结晶紫染色液浸泡20分钟,PBS洗涤3次,室温干燥。将腔室上的聚碳酸酯薄膜轻轻切割,放在玻璃载玻片上,并用中性树脂覆盖。在显微镜下计数5个随机场的细胞数,比较各组间的差异。qRT-PCR结果显示,与正常宫颈组织细胞系HCCR1相比,miR-494在宫颈癌细胞系HCCR1和C-33A中的表达水平明显降低。与转染mimics NC相比,转染miRNA-494mimics后,HCCR1mRNA和蛋白水平显著降低(P
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