miR-21 modulates resistance of HR-HPV positive cervical cancer cells to radiation through targeting LATS1

被引:65
作者
Liu, Shikai [1 ]
Song, Lili [1 ]
Zhang, Liang [1 ]
Zeng, Saitian [1 ]
Gao, Fangyuan [1 ]
机构
[1] Cangzhou Cent Hosp, Cangzhou 061001, Hebei, Peoples R China
关键词
miR-21; HR-HPV; Cervical cancer; Radioresistance; HUMAN HOMOLOG; EXPRESSION; MICRORNAS; SIGNATURE;
D O I
10.1016/j.bbrc.2015.03.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Although multiple miRNAs are found involved in radioresistance development in HR-HPV positive (+) cervical cancer, only limited studies explored the regulative mechanism of the miRNAs. miR-21 is one of the miRNAs significantly upregulated in HR-HPV (+) cervical cancer is also significantly associated with radioresistance. However, the detailed regulative network of miR-21 in radioresistance is still not clear. In this study, we confirmed that miR-21 overexpression was associated with higher level of radioresistance in HR-HPV (+) cervical cancer patients and thus decided to further explore its role. Findings of this study found miR-21 can negatively affect radiosensitivity of HR-HPV (+) cervical cancer cells and decrease radiation induced G2/M block and increase S phase accumulation. By using dual luciferase assay, we verified a binding site between miR-21 and 3'-UTR of large tumor suppressor kinase 1 (LATS1). Through direct binding, miR-21 can regulate LATS1 expression in cervical cancer cells. LATS1 overexpression can reverse miR-21 induced higher colony formation rate and also reduced miR-21 induced S phase accumulation and G2/M phase block reduction under radiation treatment. These results suggested that miR-21-LATS1 axis plays an important role in regulating radiosensitivity. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:679 / 685
页数:7
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