Department of Experimental Research, Sun Yat-sen University Cancer Center, State Key Laboratory Oncology in South China, Guangzhou, China.
The First Affiliated Hospital of Zhengzhou University, Zhengzhou University, Zhengzhou, China.
Theranostics. 2018 Mar 8;8(8):2202-2216. doi: 10.7150/thno.24003. eCollection 2018.
Metastasis is the leading cause of disease-related death among patients with nasopharyngeal carcinoma (NPC). Mounting evidence suggest that epithelial-mesenchymal transition (EMT) is crucial for cancer cells to acquire metastatic ability. In this study, we aim to clarify the extent to which EMT is involved in various cancer properties and identify novel markers for predicting the prognosis of NPC patients. Two cellular models derived from the same NPC cell line with distinct metastasis ability were used for microarray analysis to identify key transcriptional factors that drive metastasis. Cell migration and invasion were analyzed by wound healing and Transwell analysis. Lung metatasis was determined by tail vein injection assay. Cancer stemness was analyzed using colony formation and xenograft assay. The EMT extent was evaluated using immunoblotting, RT-qPCR and immunofluorescence of EMT markers. The value of OVOL2 in prognosis was determined by immunohistochemistry in NPC biopsies. OVOL2 was the most significantly down-regulated EMT transcription factor (EMT-TF) in cellular models of NPC metatasis. Low levels of OVOL2 were associated with poor overall survival of NPC patients and the reduced expression is partly due to promoter methylation and epithelial dedifferentiation. Knockout of OVOL2 in epithelial-like NPC cells partially activates EMT program and significantly promotes cancer stemness and metastatic phenotypes. Conversely, ectopically expression of OVOL2 in mesenchymal-like cells leads to a partial transition to an epithelial phenotype and reduced malignancy. Reversing EMT by depleting ZEB1, a major target of OVOL2, does not eliminate the stemness advantage of OVOL2-deficient cells but does reduce their invasion capacity. A comparison of subpopulations at different stages of EMT revealed that the extent of EMT is positively correlated with metastasis and drug resistance; however, only the intermediate EMT state is associated with cancer stemness. Distinct from other canonical EMT-TFs, OVOL2 only exhibits modest effect on EMT but has a strong impact on both metastasis and tumorigenesis. Therefore, OVOL2 could serve as a prognostic indicator for cancer patients.
转移是鼻咽癌(NPC)患者疾病相关死亡的主要原因。越来越多的证据表明,上皮-间充质转化(EMT)对于癌细胞获得转移能力至关重要。在这项研究中,我们旨在阐明 EMT 在各种癌症特性中的参与程度,并确定预测 NPC 患者预后的新标志物。
使用源自具有不同转移能力的同一 NPC 细胞系的两种细胞模型进行微阵列分析,以鉴定驱动转移的关键转录因子。通过划痕愈合和 Transwell 分析分析细胞迁移和侵袭。通过尾静脉注射测定肺转移。使用集落形成和异种移植测定分析癌症干细胞特性。通过 EMT 标志物的免疫印迹、RT-qPCR 和免疫荧光评估 EMT 程度。通过 NPC 活检的免疫组化确定 OVOL2 在预后中的价值。
在 NPC 转移的细胞模型中,OVOL2 是最显著下调的 EMT 转录因子(EMT-TF)。低水平的 OVOL2 与 NPC 患者的总体生存不良相关,并且表达减少部分归因于启动子甲基化和上皮去分化。在上皮样 NPC 细胞中敲除 OVOL2 部分激活 EMT 程序,并显著促进癌症干细胞特性和转移表型。相反,在间充质样细胞中异位表达 OVOL2 导致部分向上皮表型转化并降低恶性程度。通过耗尽 OVOL2 的主要靶标 ZEB1 逆转 EMT 并不能消除 OVOL2 缺陷细胞的干细胞优势,但会降低其侵袭能力。对 EMT 不同阶段亚群的比较表明,EMT 的程度与转移和耐药性呈正相关;然而,只有中间 EMT 状态与癌症干细胞特性相关。
与其他经典 EMT-TFs 不同,OVOL2 仅对 EMT 表现出适度的影响,但对转移和肿瘤发生有很强的影响。因此,OVOL2 可以作为癌症患者的预后指标。