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RETRACTED: Long non-coding RNA HULC promotes bladder cancer cells proliferation but inhibits apoptosis via regulation of ZIC2 and PI3K/AKT signaling pathway (Retracted article. See vol. 35, pg. 345, 2022)
被引:59
|作者:
Wang, Jintao
[1
]
Ma, Weimin
[2
]
Liu, Yidong
[3
]
机构:
[1] 4 Peoples Hosp Hengshui, Dept Urol, Hengshui 053000, Hebei, Peoples R China
[2] Binzhou City Cent Hosp, Dept Urol, Binzhou 251700, Shandong, Peoples R China
[3] Taian City Cent Hosp, Dept Urol, 29 Longtan Rd, Tai An 271000, Shandong, Peoples R China
关键词:
Bladder cancer;
lncRNA HULC;
cell proliferation;
cell apoptosis;
ZIC2;
PI3K/AKT;
LNCRNA HULC;
EXPRESSION;
INVASION;
REVEALS;
DISEASE;
SINGLE;
D O I:
10.3233/CBM-170188
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
BACKGROUND: Bladder cancer is the fourth most common malignancy among men urinary system and it is a complex disease caused by genetic and environmental factors. OBJECTIVE: This study aimed to evaluate the effects of hepatocellular carcinoma up-regulated long non-coding RNA ( lncRNA HULC) on bladder cancer and to reveal the potential mechanisms. METHODS: The expression level of HULC in 276 bladder cancer patients was detected. The association of HULC level with patient recurrence was performed by Kaplan-Meier and log-rank test. Moreover, T24 and RT4 cells were transfected with HULC and ZIC2 targeted siRNAs, HULC expressing vector and corresponding controls. Subsequently, cell viability, apoptosis and tumorigenesis were examined. RESULTS: The expression level of HULC was increased in bladder cancer tissues. High expression of HULC was correlated with advanced clinical stage and lower recurrence-free rate. HULC was remarkably promoted cell viability but inhibited apoptosis, meanwhile conspicuously increased the expression of Cyclin A/D1/E and Bcl-2. Xenograft tumor model showed that HULC promoted tumor weights in vivo. CONCLUSIONS: LncRNA HULC promoted bladder cancer cells proliferation and inhibited apoptosis.
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页码:425 / 434
页数:10
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