ETV4/CDHP轴在甲状腺乳头状癌发生发展中的作用机制研究
作者:
通讯作者:
作者单位:

1.新疆医科大学第二临床学院,新疆 乌鲁木齐 830000;2.中南大学湘雅医院 甲状腺外科,湖南 长沙 410008;3.新疆医科大学第二附属医院 肿瘤外科,新疆 乌鲁木齐 830000

作者简介:

付国德,新疆医科大学第二临床学院住院医师,主要从事甲状腺疾病基础方面的研究。

基金项目:

国家自然科学基金资助项目(82260585);国家青年科学基金资助项目(82203834)。


The oncogenic role of the ETV4/CDHP axis in papillary thyroid carcinoma
Author:
Affiliation:

1.The Second Clinical School, Xinjiang Medical University, Urumqi 830000, China;2.Department of Thyroid Surgery, Xiangya Hospital, Central South University, Changsha 410008, China;3.Department of Surgical Oncology, the Second Affiliated Hospital of Xinjiang Medical University, Urumqi 830000, China

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 音频文件
  • |
  • 视频文件
    摘要:

    背景与目的 甲状腺乳头状癌(PTC)是最常见的内分泌系统恶性肿瘤,其侵袭与转移机制尚不完全清楚。本研究旨在探讨转录因子E26转化特异性变体4(ETV4)在PTC中的作用及其与细胞黏附蛋白CDHP(CDH3)的调控关系。方法 利用TCGA与GTEx数据库分析ETV4和CDHP在PTC中的表达差异及相关性;在正常甲状腺细胞和多种PTC细胞系中检测两者的表达水平;通过siRNA构建ETV4敲低模型,采用qRT-PCR、Western blot、CCK-8、划痕及Transwell实验评估其对CDHP表达及细胞功能的影响。结果 数据库分析显示,ETV4和CDHP在PTC组织中呈高表达,癌组织与癌旁对比差异均具有统计学意义(P<0.001)。相关性分析提示ETV4与CDHP表达呈明显正相关(R2>0.5,P<0.01)。细胞实验进一步证实,四种PTC细胞系中ETV4和CDHP的mRNA及蛋白水平均高于正常甲状腺细胞(P<0.05)。在ETV4敲低模型中,CDHP表达明显下调(P<0.05),同时CCK-8法检测显示细胞增殖率下降,划痕及Transwell实验结果提示迁移和侵袭能力均明显减弱(均P<0.05)。结论 ETV4可能通过转录调控上调CDHP的表达,促进PTC细胞的增殖、迁移与侵袭。ETV4/CDHP轴有望成为PTC新的分子标志物和潜在治疗靶点。

    Abstract:

    Background and Aims Papillary thyroid carcinoma (PTC) is the most common endocrine malignancy, yet the molecular mechanisms underlying its invasion and metastasis remain unclear. This study aimed to investigate the role of the transcription factor ETV4 in PTC and its regulatory relationship with cadherin-3 (CDHP/CDH3).Methods Expression levels of ETV4 and CDHP were analyzed using TCGA and GTEx databases, and further validated in normal thyroid cells and multiple PTC cell lines by qRT-PCR and Western blot analysis. ETV4-knockdown models were established using siRNA, and changes in CDHP expression and cellular behaviors were assessed by qRT-PCR, Western blot, CCK-8, wound healing, and Transwell assays.Results Bioinformatics analysis revealed significantly higher expression of ETV4 and CDHP in PTC tissues compared to normal thyroid tissues (P<0.001). Correlation analysis demonstrated a strong positive association between ETV4 and CDHP expression (R2>0.5, P<0.01). In vitro assays confirmed that both ETV4 and CDHP were upregulated in all tested PTC cell lines at the mRNA and protein levels (all P<0.05). Knockdown of ETV4 led to marked reduction of CDHP expression (P<0.05), accompanied by decreased cell proliferation, migration, and invasion as demonstrated by CCK-8, wound healing, and Transwell assays (all P<0.05).Conclusion ETV4 may transcriptionally upregulates CDHP to promote proliferation, migration, and invasion of PTC cells. The ETV4/CDHP axis may serve as a novel biomarker and potential therapeutic target in PTC.

    图1 差异基因的筛选和验证 A:TCGA数据库筛选出高表达基因;B:TCGA数据库中50个样本进一步分析表达水平;C:正常个体与肿瘤个体ETV4表达差异比较;D:正常个体与肿瘤个体CDHP表达差异比较;E:48对癌与癌旁组织ETV4 mRNA表达水平比较;F:48对癌与癌旁组织CDHP mRNA表达水平比较Fig.1 Screening and validation of differentially expressed genes A: Identification of highly expressed genes from the TCGA database; B: Further analysis of expression levels in 50 TCGA samples; C: Comparison of ETV4 expression between normal and tumor tissues; D: Comparison of CDHP expression between normal and tumor tissues; E: Comparison of ETV4 mRNA expression levels between 48 paired tumor and adjacent normal tissues; F: Comparison of CDHP mRNA expression levels between 48 paired tumor and adjacent normal tissues
    图2 细胞水平验证ETV4及CDHP表达 A:ETV4 mRNA的表达水平;B:CDHP mRNA的表达水平;C:ETV4蛋白表达水平;D:CDHP蛋白表达水平Fig.2 Validation of ETV4 and CDHP expression at the cellular level A: Expression level of ETV4 mRNA; B: Expression level of CDHP mRNA; C: Expression level of ETV4 protein; D: Expression level of CDHP protein
    图3 ETV4与CDHP的调控关系 A:ETV4与CDHP的相关性分析;B:ETV4的motif序列;C:构建ETV4敲低模型后mRNA表达水平;D:CDHP在ETV4敲低模型中的表达Fig.3 Regulatory relationship between ETV4 and CDHP A: Correlation analysis between ETV4 and CDHP; B: Motif sequence of ETV4; C: mRNA expression levels after constructing the ETV4 knockdown model; D: CDHP expression in the ETV4 knockdown mode
    图4 ETV4对PTC细胞增殖、侵袭、迁移的影响 A:敲低ETV4对PTC细胞增殖的影响;B:敲低ETV4对PTC细胞迁移的影响(×40);C:敲低ETV4对PTC细胞侵袭的影响(×100)Fig.4 Effects of ETV4 on proliferation, invasion, and migration of PTC cells A: Effect of ETV4 knockdown on PTC cell proliferation; B: Effect of ETV4 knockdown on PTC cell migration (×40); C: Effect of ETV4 knockdown on PTC cell invasion (×100)
    表 1 引物序列Table 1 Primer sequences
    表 2 siRNA序列Table 2 siRNA sequences
    表 3 Table 3
    参考文献
    相似文献
    引证文献
引用本文

付国德,欧阳锡武,慕世纪,桂若彤,白宁. ETV4/CDHP轴在甲状腺乳头状癌发生发展中的作用机制研究[J].中国普通外科杂志,2025,34(7):1430-1439.
DOI:10.7659/j. issn.1005-6947.250069

复制
文章指标
  • 点击次数:
  • 下载次数:
历史
  • 收稿日期:2025-02-12
  • 最后修改日期:2025-07-22
  • 录用日期:
  • 在线发布日期: 2025-09-02