a Department of Cardiology , China-Japan Union Hospital of Jilin University , Jilin , China.
b Jilin Provincial Precision Medicine Key Laboratory for Cardiovascular Genetic Diagnosis , Jilin , China.
Cell Cycle. 2018;17(10):1268-1278. doi: 10.1080/15384101.2018.1475829. Epub 2018 Jul 23.
This study was aimed to explore the effects of miR-29a-5p expression and its target gene TPX2 (target protein for Xenopus kinesin-like protein 2) on endometrial cancer (EC) devel on EC development and to assess the prognostic impacts of TPX2. Microarray-based GEO and TCGA (the Cancer Genome Atlas) EC expression data were used to identify differentially expressed miRNAs and mRNAs. The observed potential target relationship between miR-29a-5p and TPX2 was verified using TargetScan and luciferase reporter assays. The mRNA and protein expression levels of miR-29a-5p and TPX2 were confirmed by qRT-PCR and western blot, respectively. Associations between TPX2 expression and patient prognosis were assessed using Kaplan-Meier and log-rank assays. Changes in EC-derived cell proliferation, invasion and apoptosis after exogenous miR-29a-5p and TPX2 over-expression and/or silencing were assessed using CCK-8 (cell counting kit-8), colony formation, Transwell and flow cytometry assays, respectively. We found that in primary EC tissues the expression of miR-29a-5p was down-regulated and the expression of TPX2 was up-regulated. We also found that low expression of TPX2 were associated with a better prognosis, and vice versa. Subsequent exogenous miR-29a-5p over-expression and TPX2 silencing could inhibit EC-derived cell proliferation and invasion, and to induce apoptosis. We also found that miR-29a-5p might target and repress TPX2, thereby inhibiting EC-derived cell proliferation and invasion and enhancing apoptosis. We conclude that miR-29a-5p could inhibit the proliferation and invasion of EC-derived cells and enhance the apoptosis of EC-derived cells via TPX2 down-regulation. A high TPX2 expression in primary EC tissues was found to be associated with a poor prognosis. As such, these biomarkers may serve as promising prognostic indicators.
EC: Endometrial cancer; 3'-UTR: 3'-untranslated regions; TPX2: target protein for Xenopus kinesin-like protein 2; TCGA: the Cancer Genome Atlas; UCEC: uterine corpus endometrial carcinoma; CCK-8: cell counting kit-8; OD: optical density; FCM: flow cytometry; EMT: epithelial-mesenchymal transition.
本研究旨在探讨 miR-29a-5p 表达及其靶基因 TPX2(Xenopus kinesin-like protein 2 的靶蛋白)对子宫内膜癌(EC)发展的影响,并评估 TPX2 的预后影响。基于微阵列的 GEO 和 TCGA(癌症基因组图谱)EC 表达数据用于鉴定差异表达的 miRNAs 和 mRNAs。使用 TargetScan 和荧光素酶报告基因测定验证 miR-29a-5p 与 TPX2 之间观察到的潜在靶关系。通过 qRT-PCR 和 Western blot 分别确认 miR-29a-5p 和 TPX2 的 mRNA 和蛋白表达水平。使用 Kaplan-Meier 和对数秩检验评估 TPX2 表达与患者预后的关系。通过 CCK-8(细胞计数试剂盒-8)、集落形成、Transwell 和流式细胞术分别评估外源性 miR-29a-5p 和 TPX2 过表达和/或沉默后 EC 衍生细胞增殖、侵袭和凋亡的变化。我们发现,在原发性 EC 组织中,miR-29a-5p 的表达下调,而 TPX2 的表达上调。我们还发现,TPX2 的低表达与更好的预后相关,反之亦然。随后外源性 miR-29a-5p 过表达和 TPX2 沉默可抑制 EC 衍生细胞的增殖和侵袭,并诱导凋亡。我们还发现,miR-29a-5p 可能靶向并抑制 TPX2,从而抑制 EC 衍生细胞的增殖和侵袭,增强凋亡。我们的结论是,miR-29a-5p 可通过下调 TPX2 抑制 EC 衍生细胞的增殖和侵袭,并增强 EC 衍生细胞的凋亡。原发性 EC 组织中高表达 TPX2 与预后不良相关。因此,这些生物标志物可能成为有前途的预后指标。
EC:子宫内膜癌;3'-UTR:3'-非翻译区;TPX2:Xenopus kinesin-like protein 2 的靶蛋白;TCGA:癌症基因组图谱;UCEC:子宫体子宫内膜癌;CCK-8:细胞计数试剂盒-8;OD:光密度;FCM:流式细胞术;EMT:上皮-间充质转化。