SPLUNC1 Regulates Cell Progression and Apoptosis through the miR-141-PTEN/p27 Pathway, but Is Hindered by LMP1

被引:19
作者
Chen, Pan [1 ,2 ,3 ,4 ]
Guo, Xiaofang [3 ,4 ]
Zhou, Houde [3 ,4 ]
Zhang, Wenling [3 ,4 ]
Zeng, Zhaoyang [1 ,2 ,3 ,4 ,5 ,6 ]
Liao, Qianjin [3 ,4 ]
Li, Xiayu [5 ,6 ]
Xiang, Bo [1 ,2 ,3 ,4 ,5 ]
Yang, Jianbo [6 ,7 ,8 ]
Ma, Jian [1 ,2 ,3 ,4 ,5 ,6 ]
Zhou, Ming [1 ,2 ,3 ,4 ,5 ,6 ]
Peng, Shuping [1 ,2 ,3 ,4 ,5 ,6 ]
Xiang, Juanjuan [1 ,2 ,3 ,4 ,5 ,6 ]
Li, Xiaoling [1 ,2 ,3 ,4 ,5 ]
Le, Colvin Wanshura [7 ,8 ]
Xiong, Wei [1 ,2 ,3 ,4 ,5 ,6 ]
McCarthy, James B. [7 ,8 ]
Li, Guiyuan [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Cent S Univ, Hunan Prov Tumor Hosp, Changsha, Hunan, Peoples R China
[2] Cent S Univ, Xiangya Med Sch, Affiliated Tumor Hosp, Changsha, Hunan, Peoples R China
[3] Cent S Univ, Key Lab Carcinogenesis, Minist Hlth, Canc Res Inst, Changsha, Hunan, Peoples R China
[4] Cent S Univ, Key Lab Carcinogenesis & Canc Invas, Canc Res Inst, Minist Educ, Changsha, Hunan, Peoples R China
[5] Cent S Univ, Xiangya Hosp 3, Hunan Key Lab Nonresolving Inflammat, Changsha, Hunan, Peoples R China
[6] Cent S Univ, Xiangya Hosp 3, Canc & Dis Genome Res Ctr, Changsha, Hunan, Peoples R China
[7] Univ Minnesota, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
[8] Univ Minnesota, Masonic Canc Ctr, Minneapolis, MN 55455 USA
来源
PLOS ONE | 2013年 / 8卷 / 03期
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
EPSTEIN-BARR-VIRUS; NF-KAPPA-B; NASOPHARYNGEAL CARCINOMA; SUSCEPTIBILITY LOCUS; CDNA MICROARRAY; INHERITED BREAST; CHROMOSOME; 3P21; HOST-DEFENSE; PROTEIN; GENE;
D O I
10.1371/journal.pone.0056929
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Little is known about the role of the host defensive protein short palate, lung and nasal epithelium clone 1 (SPLUNC1) in the carcinogenesis of nasopharyngeal carcinoma (NPC). Here we report that SPLUNC1 plays a role at a very early stage of NPC carcinogenesis. SPLUNC1 regulates NPC cell proliferation, differentiation and apoptosis through miR-141, which in turn regulates PTEN and p27 expression. This signaling axis is negatively regulated by the EBV-coded gene LMP1. Therefore we propose that SPLUNC1 suppresses NPC tumor formation and its inhibition by LMP1 provides a route for NPC tumorigenesis.
引用
收藏
页数:12
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