Long noncoding RNA HOTTIP is a significant indicator of ovarian cancer prognosis and enhances cell proliferation and invasion.

IF 1.9
Ting Zou, Ping Ling Wang, Yan Gao, Wen Tong Liang
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引用次数: 28

Abstract

Long noncoding RNAs (LncRNAs) are involved in the occurrence and progression of human tumors including ovarian cancer (OC). Long noncoding RNA HOTTIP has been found to be involved in several human tumors development. However, the role of HOTTIP in OC remains large unknown. In the present study, our results observed that lncRNA HOTTIP expression levels were notably higher in ovarian cancer tissue samples compared to adjacent normal tissue samples. Increased lncRNA HOTTIP expression levels were significantly associated with advanced FIGO stage and lymph node metastasis of ovarian cancer patients. Survival plots analysis results showed high lncRNA HOTTIP expression levels in ovarian cancer patients showed a poor prognosis compared to patients with low lncRNA HOTTIP expression levels. Function assays showed that lncRNA HOTTIP knockdown in ovarian cancer cells decreased cell proliferation and cell invasion capacities. Furthermore, we demonstrated that inhibition of lncRNA HOTTIP suppressed Wnt/β-catenin signaling by downregulating β-catenin expression. Thus, these results suggest that aberrant HOTTIP expression level could serve as a promising biomarker for monitoring ovarian cancer and potential target of ovarian cancer treatment.

长链非编码RNA HOTTIP是卵巢癌预后的重要指标,可促进细胞增殖和侵袭。
长链非编码rna (LncRNAs)参与了包括卵巢癌(OC)在内的人类肿瘤的发生和发展。长链非编码RNA HOTTIP已被发现参与了几种人类肿瘤的发展。然而,HOTTIP在OC中的作用仍然是未知的。在本研究中,我们的研究结果发现,lncRNA HOTTIP在卵巢癌组织样本中的表达水平明显高于邻近的正常组织样本。lncRNA HOTTIP表达水平升高与卵巢癌晚期FIGO分期及淋巴结转移显著相关。生存图分析结果显示,与lncRNA HOTTIP低表达的患者相比,lncRNA HOTTIP高表达的卵巢癌患者预后较差。功能分析显示,lncRNA HOTTIP敲低可降低卵巢癌细胞的增殖和细胞侵袭能力。此外,我们证明了lncRNA HOTTIP的抑制通过下调β-catenin的表达来抑制Wnt/β-catenin信号传导。因此,这些结果表明,HOTTIP的异常表达水平可以作为卵巢癌监测的生物标志物和卵巢癌治疗的潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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