生物标志物
结直肠癌
医学
肿瘤科
癌基因
恶性肿瘤
癌症
癌变
内科学
小核仁RNA
临床意义
克拉斯
转移
癌症研究
长非编码RNA
细胞周期
生物
下调和上调
生物化学
基因
作者
Yoshinaga Okugawa,Yuji Toiyama,Shusuke Toden,Hiroki Mitoma,Takeshi Nagasaka,Koji Tanaka,Yasuhiro Inoue,Masato Kusunoki,Clement Richard Boland,Ajay Goel
出处
期刊:Gut
[BMJ]
日期:2015-10-15
卷期号:66 (1): 107-117
被引量:150
标识
DOI:10.1136/gutjnl-2015-309359
摘要
PURPOSE: Despite recent advances in colorectal cancer (CRC) treatment, the prognosis of patients suffering from this malignancy still remains substandard, and metastatic recurrence following curative surgery is the leading cause of mortality. Therefore, it is imperative to identify prognostic markers to predict the clinical outcome of CRC patients. Recent evidence revealed the new role of small nucleolar RNAs (snoRNAs) in oncogenesis. Herein, we systematically evaluated dysregulation of snoRNAs in CRC and clarified their biomarker potential and biological significance in CRC. EXPERIMENTAL DESIGN: We analysed expression levels of 4 snoRNAs in 274 colorectal tissues from 3 independent cohorts and 6 colon cancer cell lines. The functional characterisation for the role of SNORA42 in CRC was investigated through a series of in vitro and in vivo experiments. RESULTS: In the screening phase, expression levels of all four snoRNAs were significantly elevated in CRC tissues than in corresponding normal mucosa. In the clinical validation cohort, increased SNORA42 expression was an independent prognostic factor for overall survival and disease-free survival, and was a risk factor for distant metastasis. SNORA42 expression negatively correlated with overall survival in an additional independent cohort and identified the patients with high risk for recurrence and poor prognosis in stage II CRC. Furthermore, in vitro and in vivo analyses showed that SNORA42 overexpression resulted in enhanced cell proliferation, migration, invasion, anoikis resistance and tumorigenicity. CONCLUSIONS: SNORA42 appears to be a novel oncogene and could serve as a promising predictive biomarker for recurrence and prognosis in patients with CRC.
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