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上调的环状RNA circ-UBE2D2通过海绵化miR-1236和miR-1287预测不良预后并促进乳腺癌进展。

Upregulated Circular RNA circ-UBE2D2 Predicts Poor Prognosis and Promotes Breast Cancer Progression by Sponging miR-1236 and miR-1287.

作者信息

Wang Yan, Li Jingruo, Du Chuang, Zhang Linfeng, Zhang Yingying, Zhang Jianhua, Wang Liuxing

机构信息

Department of Breast Surgery, The first affiliated hospital of Zhengzhou University. Zhengzhou 450003, PR China.

Department of Medical oncology, The first affiliated hospital of Zhengzhou University. Zhengzhou 450003, PR China.

出版信息

Transl Oncol. 2019 Oct;12(10):1305-1313. doi: 10.1016/j.tranon.2019.05.016. Epub 2019 Jul 20.

Abstract

Emerging evidence suggests that circular RNAs (circRNAs) are linked to the development and progression of human cancers. Nevertheless, their contribution to breast cancer (BC) is still largely unknown. In the current study, we screened and identified a novel circRNA, circ-UBE2D2, which was highly expressed in BC cell lines and tissues and was closely related to aggressive clinical features and dismal prognosis. Small interfering RNA (siRNA)-mediated circ-UBE2D2 silencing notably inhibited the proliferation, migration and invasion of BC cells, whereas circ-UBE2D2 overexpression displayed opposite effects. Mechanistically, circ-UBE2D2 was able to simultaneously function as molecular sponges of miR-1236 and miR-1287 to regulate the expression of their respective target genes. Moreover, circ-UBE2D2-induced tumor-promoting effects could be effectively blocked by miR-1236 or miR-1287 in BC cells. More importantly, therapeutic delivery of cholesterol-conjugated si-circ-UBE2D2 oligonucleotides significantly delayed tumor growth in vivo. Overall, our findings indicate that circ-UBE2D2 plays an essential oncogenic role in BC, and targeting circ-UBE2D2 may be a feasible treatment for BC patients.

摘要

新出现的证据表明,环状RNA(circRNAs)与人类癌症的发生和发展有关。然而,它们对乳腺癌(BC)的作用仍 largely unknown。在本研究中,我们筛选并鉴定了一种新的环状RNA,即circ-UBE2D2,它在乳腺癌细胞系和组织中高表达,且与侵袭性临床特征和不良预后密切相关。小干扰RNA(siRNA)介导的circ-UBE2D2沉默显著抑制了乳腺癌细胞的增殖、迁移和侵袭,而circ-UBE2D2过表达则表现出相反的效果。机制上,circ-UBE2D2能够同时作为miR-1236和miR-1287的分子海绵,以调节它们各自靶基因的表达。此外,在乳腺癌细胞中,miR-1236或miR-1287可有效阻断circ-UBE2D2诱导的肿瘤促进作用。更重要的是,胆固醇偶联的si-circ-UBE2D2寡核苷酸的治疗性递送显著延迟了体内肿瘤的生长。总体而言,我们的研究结果表明,circ-UBE2D2在乳腺癌中起着至关重要的致癌作用,靶向circ-UBE2D2可能是乳腺癌患者的一种可行治疗方法。

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