miR-374a-CCND 1-pPI3KJAKT-c-JUN feedback loop modulated by PDCD4 suppresses cell growth, metastasis, and sensitizes nasopharyngeal carcinoma to cisplatin

被引:94
|
作者
Zhen, Y. [1 ,2 ,3 ]
Fang, W. [1 ,3 ]
Zhao, M. [3 ]
Luo, R. [1 ]
Liu, Y. [3 ]
Fu, Q. [3 ]
Chen, Y. [3 ]
Cheng, C. [3 ]
Zhang, Y. [4 ]
Liu, Z. [3 ,4 ]
机构
[1] Southern Med Univ, TCM Integrated Hosp, Ctr Canc, Guangzhou, Guangdong, Peoples R China
[2] Guangdong Med Univ, Affiliated Hosp, Inst Resp Dis, Zhanjiang, Peoples R China
[3] Southern Med Univ, Canc Res Inst, Guangzhou 510515, Guangdong, Peoples R China
[4] Guangzhou Med Univ, Sch Basic Med, Dept Pathol, Guangzhou, Guangdong, Peoples R China
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; BREAST-CANCER CELLS; LUNG-CANCER; CYCLE PROGRESSION; GENE-EXPRESSION; DOWN-REGULATION; OVARIAN-CANCER; C-MYC; PROLIFERATION; PROMOTES;
D O I
10.1038/onc.2016.201
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
miR-374a has been reported to function as an oncogene during tumor pathogenesis. In this study, miR-374a is observed to reduce nasopharyngeal carcinoma (NPC) cell proliferation, migration, invasion, metastasis and cisplatin (DDP) resistance in vitro and in vivo. Mechanistic analyses indicate that miR-374a directly targets CCND1 to inactivate pPI3K/pAKT/c-JUN forming a negative feedback loop, as well as suppressing downstream signals related to cell cycle progression and epithelial mesenchymal transition (EMT). Interestingly, we also observed that miR-374a direct targeting of CCND1 is modulated by tumor suppressor PDCD4 via suppressing pPl3K/pAICT/c-JUN signaling. In clinical specimens, miR-374a was positively and negatively correlated with expression of PDCD4 and CCND1, respectively. Our studies are the first to demonstrate that the miR-374a-CCND1-pPl3K/AKT-c-JUN feedback loop induced by PDCD4 supresses NPC cell growth, metastasis and chemotherapy resistance.
引用
收藏
页码:275 / 285
页数:11
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