INPP4B is an oncogenic regulator in human colon cancer

被引:50
作者
Guo, S. T. [1 ]
Chi, M. N. [2 ]
Yang, R. H. [1 ]
Guo, X. Y. [1 ]
Zan, L. K. [3 ]
Wang, C. Y. [1 ]
Xi, Y. F. [3 ]
Jin, L. [2 ]
Croft, A. [4 ]
Tseng, H-Y [5 ]
Yan, X. G. [2 ]
Farrelly, M. [5 ]
Wang, F. H. [1 ]
Lai, F. [2 ]
Wang, J. F. [3 ]
Li, Y. P. [6 ]
Ackland, S. [4 ]
Scott, R. [5 ]
Agoulnik, I. U. [7 ]
Hondermarck, H. [5 ]
Thorne, R. F. [8 ]
Liu, T. [9 ]
Zhang, X. D. [5 ]
Jiang, C. C. [2 ]
机构
[1] Shanxi Med Univ, Affiliated Hosp, Shanxi Canc Hosp & Inst, Dept Mol Biol, Taiyuan, Shanxi, Peoples R China
[2] Univ Newcastle, Sch Med & Publ Hlth, Newcastle, NSW 2308, Australia
[3] Shanxi Canc Hosp & Inst, Dept Pathol, Taiyuan, Shanxi, Peoples R China
[4] Calvary Mater Newcastle Hosp, Dept Med Oncol, Newcastle, NSW, Australia
[5] Univ Newcastle, Sch Biomed Sci & Pharm, Newcastle, NSW 2300, Australia
[6] Shanxi Canc Hosp & Inst, Dept Colorectal Surg, Taiyuan, Shanxi, Peoples R China
[7] Herbert Wertheim Coll Med, Dept Cellular Biol & Pharmacol, Miami, FL USA
[8] Univ Newcastle, Sch Environm & Life Sci, Callaghan, NSW 2308, Australia
[9] Univ New S Wales, Childrens Canc Inst Australia Med Res, Sydney, NSW, Australia
基金
英国医学研究理事会; 中国国家自然科学基金;
关键词
LASER CAPTURE MICRODISSECTION; TUMOR-SUPPRESSOR; HUMAN-MELANOMA; BREAST-CANCER; PHOSPHORYLATION; PROTEIN; ACTIVATION; EXPRESSION; PATHWAY; ETS-1;
D O I
10.1038/onc.2015.361
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
Inositol polyphosphate 4-phosphatase type II (INPP4B) negatively regulates phosphatidylinositol 3-kinase signaling and is a tumor suppressor in some types of cancers. However, we have found that it is frequently upregulated in human colon cancer cells. Here we show that silencing of INPP4B blocks activation of Akt and serum-and glucocorticoid-regulated kinase 3 (SGK3), inhibits colon cancer cell proliferation and retards colon cancer xenograft growth. Conversely, overexpression of INPP4B increases proliferation and triggers anchorage-independent growth of normal colon epithelial cells. Moreover, we demonstrate that the effect of INPP4B on Akt and SGK3 is associated with inactivation of phosphate and tensin homolog through its protein phosphatase activity and that the increase in INPP4B is due to Ets-1-mediated transcriptional upregulation in colon cancer cells. Collectively, these results suggest that INPP4B may function as an oncogenic driver in colon cancer, with potential implications for targeting INPP4B as a novel approach to treat this disease.
引用
收藏
页码:3049 / 3061
页数:13
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