RETRACTED: APRIL Induces Tumorigenesis and Metastasis of Colorectal Cancer Cells via Activation of the PI3K/Akt Pathway (Retracted Article)

被引:34
|
作者
Wang, Guihua [1 ]
Wang, Feng [1 ]
Ding, Weifeng [1 ]
Wang, Jingchun [1 ]
Jing, Rongrong [1 ]
Li, Haiquan [1 ]
Wang, Xudong [1 ]
Wang, Yueguo [1 ]
Ju, Shaoqing [1 ]
Wang, Huimin [1 ]
机构
[1] Nantong Univ, Sch Publ Hlth, Affiliated Hosp, Dept Clin Lab Ctr, Nantong, Jiangsu, Peoples R China
来源
PLOS ONE | 2013年 / 8卷 / 01期
基金
中国国家自然科学基金;
关键词
NECROSIS-FACTOR FAMILY; KAPPA-B; PHOSPHOINOSITIDE; 3-KINASE; UP-REGULATION; MEMBER APRIL; C-MYC; PROLIFERATION; EXPRESSION; MATRIX-METALLOPROTEINASE-9; INHIBITION;
D O I
10.1371/journal.pone.0055298
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
A proliferation-inducing ligand (APRIL) is highly expressed in colorectal cancer (CRC) tissues and cell lines. However, the biological functions and precise signals elicited by APRIL in CRC have not been fully understood. Here, we used small interfering RNA to selectively deplete APRIL and to determine its tumorigenic effects in a CRC cell line SW480 both in vitro and in vivo. Knockdown of APRIL in SW480 cells was associated with modulation of cell proliferation as well as reduction of cell migration and invasion in vitro. Moreover APRIL-knockdown SW480 cells displayed markedly inhibited tumor growth and decreased metastasis to the liver in immunodeficient mice upon subcutaneous injection. Importantly, we observed that downregulation of APRIL in SW480 cells resulted in greatly decreased activity of phosphoinositide 3-kinase (PI3K)/Akt pathway. In addition, we observed that recombinant human APRIL mediated activation of the PI3K/Akt pathway in CRC cells resulting in induced expression of important cell cycle proteins and matrix metalloproteinases in a PI3K/Akt dependent manner. This was concurrent with marked cell growth viability as well as increased cell migration and invasion. Together, these compelling data suggest that APRIL-induced tumorigenesis and metastasis of CRC cells may be accomplished through activation of the PI3K/Akt pathway. These findings may lead to a better understanding of the biological effects of APRIL and may provide clues for identifying novel therapeutic and preventive molecular markers for CRC.
引用
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页数:14
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