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ZIC2 通过激活 Notch 信号通路上调 lncRNA SNHG12 的表达,促进子宫内膜癌细胞的增殖和迁移。

ZIC2 upregulates lncRNA SNHG12 expression to promote endometrial cancer cell proliferation and migration by activating the Notch signaling pathway.

机构信息

Department of Obstetrics and Gynecology, Dongguan People's Hospital, Dongguan, Guangdong 523000, P.R. China.

Department of Obstetrics and Gynecology, Midwifery Profession, Shanxi Health Vocational College, Jinzhong, Shanxi 030600, P.R. China.

出版信息

Mol Med Rep. 2021 Sep;24(3). doi: 10.3892/mmr.2021.12271. Epub 2021 Jul 19.

Abstract

It was previously reported that long non‑coding RNA (lncRNA) small nucleolar RNA host gene 12 (SNHG12) promoted the proliferation, invasion and migration of endometrial cancer (EC) cells; however, the upstream underlying mechanism remains unclear. The present study aimed to determine the possible underlying mechanism of SNHG12 regulating EC. The Encyclopedia of RNA Interactomes database was used to analyze whether SNHG12 could bind to Zic family member 2 (ZIC2) and the expression levels of ZIC2 in patients with EC. ZIC2 expression levels in EC cell lines were analyzed using western blotting and reverse transcription‑quantitative PCR. RL95‑2 cells were subsequently transfected with short hairpin RNA targeting ZIC2, or ZIC2 or SNHG12 overexpression plasmids. Cell proliferation, migration and invasion were analyzed using Cell Counting Kit‑8, colony formation, wound healing and Transwell assays, respectively. The binding between ZIC2 and SHNG12 was verified using dual luciferase reporter and chromatin immunoprecipitation assays. The results of the present study revealed that the expression levels of ZIC2 were upregulated in the tissues of patients with EC and EC cell lines. ZIC2 knockdown inhibited RL95‑2 cell proliferation, migration and invasion. The protein expression levels of Ki67, proliferating cell nuclear antigen, MMP2 and MMP9 were also downregulated following the knockdown of ZIC2. ZIC2 was predicted to bind to SNHG12 and positively regulate SNHG12 expression. Further experiments demonstrated that the effects of the knockdown of ZIC2 on RL95‑2 cells were partially reversed by SNHG12 overexpression. In addition, ZIC2 knockdown inhibited Notch signaling activation, while SNHG12 overexpression reversed this effect. In conclusion, the findings of the present study indicated that ZIC2 may upregulate SNHG12 expression to promote EC cell proliferation and migration by activating the Notch signaling pathway.

摘要

先前有研究报道称,长链非编码 RNA(lncRNA)小核仁 RNA 宿主基因 12(SNHG12)可促进子宫内膜癌(EC)细胞的增殖、侵袭和迁移;然而,其上游潜在机制尚不清楚。本研究旨在探讨 SNHG12 调节 EC 的潜在机制。本研究利用 RNA 相互作用组百科全书数据库分析 SNHG12 是否与锌指蛋白家族成员 2(ZIC2)结合,以及 ZIC2 在 EC 患者中的表达水平。采用 Western blot 法和逆转录-定量 PCR 法检测 EC 细胞系中 ZIC2 的表达水平。随后用靶向 ZIC2 的短发夹 RNA、ZIC2 或 SNHG12 过表达质粒转染 RL95-2 细胞。采用细胞计数试剂盒-8 法、集落形成实验、划痕愈合实验和 Transwell 实验分别分析细胞增殖、迁移和侵袭。采用双荧光素酶报告基因和染色质免疫沉淀实验验证 ZIC2 与 SHNG12 的结合。本研究结果表明,ZIC2 在 EC 组织和 EC 细胞系中表达上调。ZIC2 敲低抑制 RL95-2 细胞的增殖、迁移和侵袭。ZIC2 敲低后 Ki67、增殖细胞核抗原、MMP2 和 MMP9 的蛋白表达水平也下调。预测 ZIC2 与 SNHG12 结合并正向调节 SNHG12 表达。进一步的实验表明,SNHG12 过表达部分逆转了 ZIC2 敲低对 RL95-2 细胞的影响。此外,ZIC2 敲低抑制 Notch 信号通路的激活,而过表达 SNHG12 逆转了这一效应。综上所述,本研究结果表明,ZIC2 可能通过激活 Notch 信号通路上调 SNHG12 表达,促进 EC 细胞的增殖和迁移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/762a/8281313/b2f3fc093daf/mmr-24-03-12271-g00.jpg

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