miR-24-3p promotes cell migration and proliferation in lung cancer by targeting SOX7

被引:94
作者
Yan, Liang [1 ,2 ]
Ma, Jinzhu [2 ]
Zhu, Yiping [3 ]
Zan, Jiawei [1 ]
Wang, Zhen [3 ]
Ling, Liefeng [2 ]
Li, Qiang [2 ]
Lv, Jun [2 ]
Qi, Shimei [2 ]
Cao, Yingya [3 ]
Liu, Ying [2 ]
Cao, Long [2 ]
Zhang, Yao [2 ]
Qi, Zhilin [2 ]
Nie, Liuwang [1 ]
机构
[1] Anhui Normal Univ, Sch Life Sci, Prov Key Lab Conservat & Exploitat Res Biol Resou, Wuhu, Anhui, Peoples R China
[2] Wannan Med Coll, Prov Key Lab Biol Macromol Res, Wuhu, Anhui, Peoples R China
[3] Wannan Med Coll, Affiliated Hosp 1, Wuhu, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
lung cancer; miR-24-3p; SOX7; TUMOR-SUPPRESSOR; INVASION; METASTASIS; CARCINOMA; APOPTOSIS; PATHWAY; GROWTH;
D O I
10.1002/jcb.26553
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
Lung cancer (LC) is one of the leading causes of cancer-related death in the world. miR-24-3p plays critical roles in many cancer types, including LC. In this study, we first investigated whether miR-24-3p promoted LC cell migration and proliferation in vitro. We used three bioinformatics algorithms to predict the miR-24-3p target gene to study the molecular mechanism by which miR-24-3p contributes to LC progression. Then, we used the luciferase reporter assay to identify whether SOX7 was a direct target of miR-24-3p. Moreover, Western blotting and a quantitative real time-polymerase chain reaction analysis showed that miR-24-3p downregulated SOX7 protein expression by a post-transcriptional mechanism. Finally, we determined that SOX7 had opposing effects to those of miR-24-3p on LC cell proliferation and migration, suggesting that miR-24-3p promotes cell proliferation and migration by directly targeting SOX7. Furthermore, miR-24-3p accelerated tumor growth in xenograft mice by targeting SOX7. These results provide the first clue that miR-24-3p could play a role as an oncomiR in LC by regulating SOX7.
引用
收藏
页码:3989 / 3998
页数:10
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