Department of Gastroenterology, Second Affiliated Hospital, Shantou University Medical College, Shantou, Guangdong 515041, P.R. China.
Department of Information, Second Affiliated Hospital, Shantou University Medical College, Shantou, Guangdong 515041, P.R. China.
Oncol Rep. 2020 Nov;44(5):2130-2142. doi: 10.3892/or.2020.7754. Epub 2020 Sep 7.
Esophageal squamous cell carcinoma (ESCC) is the main subtype of esophageal cancer in China, and the prognosis of patients remains poor mainly due to the occurrence of lymph node and distant metastasis. The long non‑coding RNA (lncRNA) maternally expressed gene 3 (MEG3) has been shown to have tumor‑suppressive properties and to play an important role in epithelial‑to‑mesenchymal transition (EMT) in some solid tumors. However, whether MEG3 is involved in EMT in ESCC remains unclear. In the present study, the MEG3 expression level and its association with tumorigenesis were determined in 43 tumor tissues of patients with ESCC and in ESCC cells using reverse transcription‑quantitative PCR analysis. Gene microarray analysis was performed to detect differentially expressed genes (DEGs). Based on the functional annotation results, the effects of ectopic expression of MEG3 on cell growth, migration, invasion and EMT were assessed. MEG3 expression level was found to be markedly lower in tumor tissues and cells. Statistical analysis revealed that MEG3 expression was significantly negatively associated with lymph node metastasis and TNM stage in ESCC. Fluorescence in situ hybridization assay demonstrated that MEG3 was expressed mainly in the nucleus. Ectopic expression of MEG3 inhibited cell proliferation, migration, invasion and cell cycle progression in EC109 cells. Gene microarray results demonstrated that 177 genes were differentially expressed ≥2.0 fold in MEG3‑overexpressing cells, including 23 upregulated and 154 downregulated genes. Functional annotation revealed that the DEGs were mainly involved in amino acid biosynthetic process, mitogen‑activated protein kinase signaling, and serine and glycine metabolism. Further experiments indicated that the ectopic expression of MEG3 significantly suppressed cell proliferation, migration, invasion and EMT by downregulating phosphoserine aminotransferase 1 (PSAT1). In pathological tissues, PSAT1 and MEG3 were significantly negatively correlated, and high expression of PSAT1 predicted poor survival. Taken together, these results suggest that MEG3 may be a useful prognostic biomarker and may suppress EMT by inhibiting the PSAT1‑dependent glycogen synthase kinase‑3β/Snail signaling pathway in ESCC.
食管鳞状细胞癌(ESCC)是中国食管癌的主要亚型,患者的预后仍然较差,主要是由于发生淋巴结和远处转移。长链非编码 RNA(lncRNA)母系表达基因 3(MEG3)已被证明具有肿瘤抑制特性,并在某些实体瘤的上皮-间充质转化(EMT)中发挥重要作用。然而,MEG3 是否参与 ESCC 的 EMT 仍然不清楚。在本研究中,通过逆转录-定量 PCR 分析,检测了 43 例 ESCC 患者肿瘤组织和 ESCC 细胞中的 MEG3 表达水平及其与肿瘤发生的关系。进行基因微阵列分析以检测差异表达基因(DEGs)。根据功能注释结果,评估了异位表达 MEG3 对细胞生长、迁移、侵袭和 EMT 的影响。结果发现,肿瘤组织和细胞中的 MEG3 表达水平明显降低。统计分析显示,MEG3 的表达与 ESCC 的淋巴结转移和 TNM 分期显著负相关。荧光原位杂交试验表明,MEG3 主要表达于细胞核内。EC109 细胞中异位表达 MEG3 可抑制细胞增殖、迁移、侵袭和细胞周期进程。基因微阵列结果表明,MEG3 过表达细胞中有 177 个基因差异表达≥2.0 倍,其中上调基因 23 个,下调基因 154 个。功能注释表明,差异表达基因主要参与氨基酸生物合成过程、丝裂原激活蛋白激酶信号转导以及丝氨酸和甘氨酸代谢。进一步的实验表明,MEG3 异位表达通过下调磷酸丝氨酸转氨酶 1(PSAT1)显著抑制细胞增殖、迁移、侵袭和 EMT。在病理组织中,PSAT1 和 MEG3 呈显著负相关,PSAT1 高表达预示着预后不良。综上所述,这些结果表明,MEG3 可能是一种有用的预后生物标志物,通过抑制 PSAT1 依赖性糖原合酶激酶-3β/Snail 信号通路,抑制 EMT。