Gastrointestinal Surgery, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Jiangxi Medical College of Nanchang University, Nanchang, China.
Aging (Albany NY). 2020 Jun 6;12(12):11653-11666. doi: 10.18632/aging.103331.
Increasing evidence suggests long non-coding RNAs (lncRNAs) are distinctively expressed in several cancers. However, the functions of these lncRNAs in cancer development remain unknown. In the current study, we report high expression of a novel lncRNA, RP11-59H7.3, and its association with prognosis in colorectal cancer (CRC) patients. Functional analyses of this lncRNA revealed its role in promoting proliferation and progression of the cell cycle, as well as enhancement of cell migration and invasion. Furthermore, our results revealed that knockdown of RP11-59H7.3 promoted cell apoptosis, with luciferase reporter assays showing that it directly binds to miR-139-5p. Knockdown of this lncRNA significantly reduced expression of NOTCH1, a direct target of miR-139-5p. Additionally, we show that suppression NOTCH1 by miR-139-5p could be partially rescued by overexpressing RP11-59H7.3. Analysis of the relationship between RP11-59H7.3 and miR-139-5p, in CRC tissues, showed a negative correlation while a positive association was observed between the RP11-59H7.3 expression and levels of NOTCH1. Taken together, these results demonstrated that the RP11-59H7.3/miR-139-5p/NOTCH1 axis functions as a key regulator in CRC metastasis. RP11-59H7.3 represents a potential biomarker for CRC diagnosis and could be an important target for development of novel therapies to manage the disease.
越来越多的证据表明,长非编码 RNA(lncRNA)在几种癌症中特异性表达。然而,这些 lncRNA 在癌症发展中的功能仍然未知。在本研究中,我们报告了一种新型 lncRNA,RP11-59H7.3 的高表达及其与结直肠癌(CRC)患者预后的关系。对这种 lncRNA 的功能分析表明,它在促进细胞增殖和细胞周期进展,以及增强细胞迁移和侵袭方面发挥作用。此外,我们的结果表明,敲低 RP11-59H7.3 可促进细胞凋亡,荧光素酶报告实验表明,它可直接与 miR-139-5p 结合。敲低这种 lncRNA 可显著降低 NOTCH1 的表达,NOTCH1 是 miR-139-5p 的直接靶标。此外,我们还表明,通过 miR-139-5p 抑制 NOTCH1 可部分通过过表达 RP11-59H7.3 得到挽救。对 CRC 组织中 RP11-59H7.3 和 miR-139-5p 的关系进行分析,显示两者呈负相关,而 RP11-59H7.3 的表达与 NOTCH1 水平呈正相关。综上所述,这些结果表明,RP11-59H7.3/miR-139-5p/NOTCH1 轴在 CRC 转移中作为关键调节剂发挥作用。RP11-59H7.3 代表了 CRC 诊断的潜在生物标志物,并且可能是开发新型疗法来治疗该疾病的重要靶点。