Ji Lili, Chen Wenying, Fan Xing, Zhou Feng, Deng Xuedong, Gu Jun
Department of Ultrasonography, The Affiliated Infectious Disease Hospital of Soochow University Suzhou, Jiangsu Province, PR China.
Center for Medical Ultrasound, The Affiliated Suzhou Hospital of Nanjing Medical University Suzhou, Jiangsu Province, PR China.
Am J Transl Res. 2020 Feb 15;12(2):531-540. eCollection 2020.
In previous studies, numerous differential lncRNAs were identified via RNA-sequencing. In this dysregulated lncRNAs, lincRNA02471 attracted our attention due to its highest fold change. The aims of our study mainly focused on the function and mechanism of lincRNA02471 in papillary thyroid cancer.
Overexpression and knockdown vectors were constructed to investigate the function of lincRNA02471. Proliferation, apoptosis, invasion and EMT were performed to assess the function of lincRNA02471. Dual-luciferase reporter assay was performed to explore the relationship between lincRNA02471 and miR-758.
We found that lincRNA02471 was manifestly upregulated in papillary cancer tissues. Overexpression of lincRNA02471 significantly promoted the cell proliferation, invasion and inhibited cell apoptosis. Knockdown of lincRNA02471 inhibited the cancer development. We also found that lincRNA02471 negatively regulate miR-758 in papillary thyroid cancer. miR-758 can restore the effect of lincRNA02471. Besides, we identified that HIPK3 was the direct target of miR-758.
we performed comprehensive study of lincRNA02471 and explore its function and mechanism in papillary thyroid cancer. lincRNA02471 can sponge miR-758 and positively regulate HIPK3 to promote papillary thyroid cancer development. Our study provides new target for clinical treatment and new clues for understanding the molecular mechanism of cancer development.
在先前的研究中,通过RNA测序鉴定了许多差异lncRNA。在这些失调的lncRNA中,lincRNA02471因其最大的倍数变化而引起我们的关注。我们研究的目的主要集中在lincRNA02471在甲状腺乳头状癌中的功能和机制。
构建过表达和敲低载体以研究lincRNA02471的功能。进行增殖、凋亡、侵袭和EMT实验以评估lincRNA02471的功能。进行双荧光素酶报告基因检测以探讨lincRNA02471与miR-758之间的关系。
我们发现lincRNA02471在乳头状癌组织中明显上调。lincRNA02471的过表达显著促进细胞增殖、侵袭并抑制细胞凋亡。敲低lincRNA02471可抑制癌症发展。我们还发现lincRNA02471在甲状腺乳头状癌中负向调节miR-758。miR-758可恢复lincRNA02471的作用。此外,我们确定HIPK3是miR-758的直接靶标。
我们对lincRNA02471进行了全面研究,并探讨了其在甲状腺乳头状癌中的功能和机制。lincRNA02471可结合miR-758并正向调节HIPK3以促进甲状腺乳头状癌的发展。我们的研究为临床治疗提供了新靶点,并为理解癌症发展的分子机制提供了新线索。