Abnormal expression of TRIB3 in colorectal cancer: a novel marker for prognosis

被引:71
|
作者
Miyoshi, N. [1 ]
Ishii, H. [1 ,2 ]
Mimori, K. [2 ]
Takatsuno, Y. [2 ]
Kim, H. [1 ]
Hirose, H. [1 ]
Sekimoto, M. [1 ]
Doki, Y. [1 ]
Mori, M. [1 ,2 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Surg Gastroenterol, Suita, Osaka 5650871, Japan
[2] Kyushu Univ, Med Inst Bioregulat, Dept Mol & Cellular Biol, Div Mol & Surg Oncol, Beppu, Oita 8740838, Japan
关键词
TRIB3; prognosis; metastasis; colorectal cancer; COLON-CANCER; RANDOMIZED-TRIAL; OPEN COLECTOMY; BREAST-CANCER; CELL-LINES; ASSISTED COLECTOMY; INSULIN-RESISTANCE; TRIBBLES ORTHOLOG; KINASE-ACTIVITY; TRB3;
D O I
10.1038/sj.bjc.6605361
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: TRIB3 is a human homologue of Drosophila tribbles. Previous studies have shown that TRIB3 controls the cell growth through ubiquitination-dependent degradation of other proteins, whereas its significance in the prognosis of colorectal cancer (CRC) is not yet fully understood. MATERIALS: This study comprised 202 patients who underwent surgery for CRC, as well as 22 cell lines derived from human gastrointestinal cancer. The correlation of gene expression with clinical parameters in patients was assessed. The biological significance was evaluated by knockdown experiments in seven colorectal cancer cell lines. RESULTS: A total of 20 cancer cell lines (90.9%) expressed the TRIB3 gene. The assessment in surgical specimens indicated that the gene expression was significantly higher in the cancerous region than in the marginal non-cancerous region. Patients with high TRIB3 expression were statistically susceptible to a recurrence of the disease, and showed poorer overall survival than those with low expression. The assessment of TRIB3 knockdown in five cell lines showed that small interfering RNA (siRNA) inhibition resulted in a statistically significant reduction in cell growth. CONCLUSION: These data strongly suggest the usefulness of TRIB3 as a marker for predicting the prognosis of CRC patients, showing a basis for the development of effective treatments for CRC. British Journal of Cancer (2009) 101, 1664-1670. doi: 10.1038/sj.bjc.6605361 www.bjcancer.com (C) 2009 Cancer Research UK
引用
收藏
页码:1664 / 1670
页数:7
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