scholarly journals A serum-circulating long noncoding RNA signature can discriminate between patients with clear cell renal cell carcinoma and healthy controls

Oncogenesis ◽  
2016 ◽  
Vol 5 (2) ◽  
pp. e192-e192 ◽  
Author(s):  
Y Wu ◽  
Y-Q Wang ◽  
W-W Weng ◽  
Q-Y Zhang ◽  
X-Q Yang ◽  
...  
2019 ◽  
Vol Volume 12 ◽  
pp. 4729-4740 ◽  
Author(s):  
Junyao Duan ◽  
Xin Ma ◽  
Jing Shi ◽  
Yundong Xuan ◽  
Hanfeng Wang ◽  
...  

2018 ◽  
Vol Volume 11 ◽  
pp. 5631-5646 ◽  
Author(s):  
Changlin Wang ◽  
Gang Wang ◽  
Zijian Zhang ◽  
Zichun Wang ◽  
Minghua Ren ◽  
...  

2017 ◽  
Vol 21 (1) ◽  
pp. 55-63 ◽  
Author(s):  
Xu Bao ◽  
Junyao Duan ◽  
Yongji Yan ◽  
Xin Ma ◽  
Yu Zhang ◽  
...  

2020 ◽  
Vol 2020 ◽  
pp. 1-13
Author(s):  
Zhanxin Liu ◽  
Zichun Wang ◽  
Xiaoxiong Wang ◽  
Meisong Lu ◽  
Guang Chen

Several studies have indicated that HOXA transcript at the distal tip (HOTTIP) play important roles in the tumorigenesis and development of various cancers. We aim to investigate the expression and prognostic value of HOTTIP in clear cell renal cell carcinoma (ccRCC). A systematic review of PubMed, Embase, Medline, and Web of Science databases was performed to select eligible literatures relevant to the correlation between HOTTIP expression and clinical outcome of different cancers. The association between the HOTTIP level and overall survival (OS), lymph node metastasis (LNM), or clinical stage was subsequently analyzed. Survival analyses were performed in a large cohort of more than 500 patients with ccRCC from The Cancer Genome Atlas (TCGA) using bioinformatic methods. Seventeen studies with a total of 1594 patients with thirteen kinds of carcinomas were included in this analysis. The result showed that high HOTTIP expression could predict worse outcome in cancer patients, with the pooled hazard ratio (HR) of 2.34 (95% confidence interval (CI) 1.96–2.79, p<0.0001). The result also showed that elevated HOTTIP expression was correlated with more LNM (OR=2.61, 95% CI 1.91-3.58, p<0.0001) and advanced clinical stage (OR=3.57, 95% CI 2.58-4.93, p<0.0001). We further validated that ccRCC patients with higher HOTTIP expression tend to have unsatisfactory outcomes both in the entire TCGA dataset and different clinical stratums, like age, grade, and stage. The tumor of those patients was associated with a larger size, easier to metastasis, advanced clinical stage, and a higher pathological grade. These findings suggested that increased HOTTIP expression might act as a novel prognostic marker for ccRCC patients.


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