RETRACTED: Interaction between miR-572 and PPP2R2C, and their effects on the proliferation, migration, and invasion of nasopharyngeal carcinoma (NPC) cells (Retracted article. See MAR, 2023)

被引:14
作者
Yan, Lei [1 ]
Cai, Kerui [1 ]
Liang, Jun [1 ]
Liu, Haifeng [2 ]
Liu, Yang [3 ]
Gui, Jinqiu [3 ]
机构
[1] Mudanjiang Med Univ, Dept Histol & Embryol, Mudanjiang 157011, Heilongjiang, Peoples R China
[2] Mudanjiang Med Univ, Heilongjiang Key Lab Antifibrosis Biotherapy, Mudanjiang 157011, Heilongjiang, Peoples R China
[3] Mudanjiang Med Univ, Dept Pathogen Microbiol & Immunol, 3 Tongxiang St, Mudanjiang 157011, Heilongjiang, Peoples R China
关键词
nasopharyngeal carcinoma (NPC); miR-572; PPP2R2C; UP-REGULATION; CANCER; EXPRESSION; MICRORNAS; METASTASIS; ACTIVATION; MECHANISM; GROWTH; RNAS;
D O I
10.1139/bcb-2016-0237
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We investigated the how miR-572 regulates PPP2R2C, and studied the effects of miR-572 and PPP2R2C on proliferation and migration as well as invasion of nasopharyngeal carcinoma (NPC) cells. NPC tissues and normal tissues were collected, and the expressions of miR-572 and PPP2R2C were detected by real-time PCR. Western blot was applied to detect the expression of PPP2R2C protein. The target relationship between miR-572 and PPP2R2C was confirmed by dual luciferase reporter gene assay. MTT assay and flow cytometry were applied to investigate the viability and apoptosis levels of NPC cells. Transwell as well as wound healing assays were used, respectively, to detect the invasiveness and migration of NPC cells. MiR-572 was highly expressed in NPC tissues as well as NPC cells, and there was lower expression of PPP2R2C in NPC tissues compared with normal samples. MiR-572 could bind to the 3'UTR of PPP2R2C and decrease its expression. Over-expressed miR-572 and decreased PPP2R2C expression could both inhibit proliferation and invasion and induce apoptosis of NPC cells. Thus, miR-572 promotes the proliferation and invasion of NPC by directly down-regulating PPP2R2C.
引用
收藏
页码:578 / 584
页数:7
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