• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

唾液腺黏液表皮样癌中OCT4和MENA的免疫分析

OCT4 and MENA immunoprofiling in salivary mucoepidermoid carcinoma.

作者信息

Samir Omnia, Farag Doaa A, Ali Khadiga M, Ismail Lawahez El M

机构信息

Department of Oral Pathology, Faculty of Dentistry, Mansoura University, Mansoura, Egypt.

Department of Pathology, Faculty of Medicine, Mansoura University, Mansoura, Egypt.

出版信息

Diagn Pathol. 2025 May 27;20(1):67. doi: 10.1186/s13000-025-01665-8.

DOI:10.1186/s13000-025-01665-8
PMID:40426241
Abstract

BACKGROUND

Mucoepidermoid carcinoma (MEC) emblematizes the predominant malignant salivary gland neoplasm, characterized by its heterogeneous morphological features and diverse clinical representations. The expression patterns and prognostic significance of Octamer transcription factor 4 (OCT4) and Mammalian-enabled (MENA) protein in MEC perdure are incompletely described.

METHODS

Immunohistochemical analysis was performed on 46 archival MEC specimens and 5 normal salivary-gland controls. OCT4 and MENA staining were assessed histomorphometrically and correlated with clinicopathological parameters. Statistical analysis comprised Monte Carlo and Spearman's correlation tests.

RESULTS

OCT4 revealed selective cytoplasmic immunoreactivity in intermediate and epidermoid cells, without nuclear positivity. Strong OCT4 expression predominated in low-grade (66.7%), while high-grade MEC exhibited variable immunoreactivity, with 53% showing weak expression. No significant correlation was found between OCT4 expression and clinical or pathological data. MENA showed cytoplasmic and membranous immunolocalization, with expression patterns correlated significantly with age (p = 0.015), tumor size (p = 0.012), clinical stage (p = 0.004), and histological grading (p = 0.001). Spearman's correlation analysis revealed a weak, non-significant association between OCT4 and MENA expression (r = 0.05, p = 0.744).

CONCLUSIONS

The differential expression patterns of OCT4 and MENA in MEC prognosticate distinct regulatory mechanisms. While OCT4 cytoplasmic expression may presage early involvement in carcinogenesis, MENA cellular expression portends potentially independent molecular pathways, possibly encompassing subnetworks in the Wnt/β-catenin and TGF-β signaling cascades. MENA may serve as a biomarker for predicting the aggressive behavior of MEC.

摘要

背景

黏液表皮样癌(MEC)是主要的恶性唾液腺肿瘤,其形态特征多样,临床表现各异。八聚体转录因子4(OCT4)和哺乳动物 Enabled 蛋白(MENA)在 MEC 中的表达模式及预后意义尚未完全阐明。

方法

对46例存档的 MEC 标本和5例正常唾液腺对照进行免疫组织化学分析。采用组织形态计量学方法评估 OCT4 和 MENA 染色情况,并与临床病理参数进行相关性分析。统计分析包括蒙特卡洛检验和 Spearman 相关性检验。

结果

OCT4 在中间细胞和表皮样细胞中显示出选择性的细胞质免疫反应性,无核阳性。OCT4 强表达在低级别 MEC 中占主导(66.7%),而高级别 MEC 表现出不同的免疫反应性,53%表现为弱表达。未发现 OCT4 表达与临床或病理数据之间存在显著相关性。MENA 显示出细胞质和细胞膜免疫定位,其表达模式与年龄(p = 0.015)、肿瘤大小(p = 0.012)、临床分期(p = 0.004)和组织学分级(p = 0.001)显著相关。Spearman 相关性分析显示 OCT4 和 MENA 表达之间存在微弱且无统计学意义的关联(r = 0.05,p = 0.744)。

结论

OCT4 和 MENA 在 MEC 中的差异表达模式预示着不同的调控机制。虽然 OCT4 的细胞质表达可能预示着早期参与致癌过程,但 MENA 的细胞表达预示着潜在的独立分子途径,可能包括 Wnt/β-连环蛋白和 TGF-β 信号级联中的子网络。MENA 可能作为预测 MEC 侵袭性行为的生物标志物。

相似文献

1
OCT4 and MENA immunoprofiling in salivary mucoepidermoid carcinoma.唾液腺黏液表皮样癌中OCT4和MENA的免疫分析
Diagn Pathol. 2025 May 27;20(1):67. doi: 10.1186/s13000-025-01665-8.
2
Embryonic stem cells markers Oct4 and Nanog correlate with perineural invasion in human salivary gland mucoepidermoid carcinoma.胚胎干细胞标志物Oct4和Nanog与人类涎腺黏液表皮样癌的神经周浸润相关。
J Oral Pathol Med. 2017 Feb;46(2):112-120. doi: 10.1111/jop.12449. Epub 2016 May 1.
3
Immunohistochemical expression of epithelial cell adhesion molecule (EpCAM) in mucoepidermoid carcinoma compared to normal salivary gland tissues.与正常唾液腺组织相比,黏液表皮样癌中上皮细胞黏附分子(EpCAM)的免疫组化表达。
Arch Oral Biol. 2017 Jul;79:87-94. doi: 10.1016/j.archoralbio.2017.03.014. Epub 2017 Mar 21.
4
Bcl-2 protein expression in mucoepidermoid carcinoma of salivary glands: a single institution experience.唾液腺黏液表皮样癌中Bcl-2蛋白表达:单机构经验
Hematol Oncol Stem Cell Ther. 2012;5(2):96-100. doi: 10.5144/1658-3876.2012.96.
5
Immunohistochemical expression profiles of mucin antigens in salivary gland mucoepidermoid carcinoma: MUC4- and MUC6-negative expression predicts a shortened survival in the early postoperative phase.涎腺黏液表皮样癌中黏蛋白抗原的免疫组化表达谱:MUC4和MUC6阴性表达预示术后早期生存期缩短。
Histol Histopathol. 2018 Feb;33(2):201-213. doi: 10.14670/HH-11-913. Epub 2017 Jun 26.
6
Expression of Mucins in Salivary Gland Mucoepidermoid Carcinoma.涎腺黏液表皮样癌中黏蛋白的表达。
Head Neck Pathol. 2021 Jun;15(2):491-502. doi: 10.1007/s12105-020-01226-z. Epub 2020 Sep 21.
7
Molecular differences in mucoepidermoid carcinoma and adenoid cystic carcinoma of the major salivary glands.大唾液腺黏液表皮样癌和腺样囊性癌的分子差异
Laryngoscope. 2001 Aug;111(8):1373-8. doi: 10.1097/00005537-200108000-00011.
8
The Utility of BSND Immunohistochemistry in the Differential Diagnosis of Oncocytic and Warthin-like Mucoepidermoid Carcinoma of Salivary Gland.BSND 免疫组化在涎腺嗜酸细胞性和沃辛样黏液表皮样癌鉴别诊断中的应用。
Head Neck Pathol. 2024 Nov 26;18(1):123. doi: 10.1007/s12105-024-01728-0.
9
"Pancreatic Mucoepidermoid Carcinoma" Is not a Pancreatic Counterpart of CRTC1/3-MAML2 Fusion Gene-related Mucoepidermoid Carcinoma of the Salivary Gland, and May More Appropriately be Termed Pancreatic Adenosquamous Carcinoma With Mucoepidermoid Carcinoma-like Features.“胰腺黏液表皮样癌”并非唾液腺 CRTC1/3-MAML2 融合基因相关黏液表皮样癌的胰腺对应物,而更恰当地称为具有黏液表皮样癌样特征的胰腺腺鳞癌。
Am J Surg Pathol. 2018 Nov;42(11):1419-1428. doi: 10.1097/PAS.0000000000001135.
10
Pathologic grading of mucoepidermoid carcinomas of the salivary gland and its effect on clinicopathologic follow-up: an institutional experience.涎腺黏液表皮样癌的病理分级及其对临床病理随访的影响:机构经验。
Hum Pathol. 2020 Apr;98:89-97. doi: 10.1016/j.humpath.2020.02.001. Epub 2020 Feb 6.

本文引用的文献

1
Transcriptional regulation of cancer stem cell: regulatory factors elucidation and cancer treatment strategies.癌症干细胞的转录调控:调控因子的阐明和癌症治疗策略。
J Exp Clin Cancer Res. 2024 Apr 2;43(1):99. doi: 10.1186/s13046-024-03021-y.
2
Expression of isoforms is reduced in primary colorectal cancer.原发性结直肠癌中同工型的表达降低。
Front Oncol. 2023 Jun 20;13:1166835. doi: 10.3389/fonc.2023.1166835. eCollection 2023.
3
Overexpression of Mena is associated with tumor progression and poor prognosis in oral squamous cell carcinoma EMT.
Mena的过表达与口腔鳞状细胞癌EMT中的肿瘤进展和不良预后相关。
Front Oncol. 2022 Dec 23;12:1052375. doi: 10.3389/fonc.2022.1052375. eCollection 2022.
4
Actin Cytoskeleton and Regulation of TGFβ Signaling: Exploring Their Links.肌动蛋白细胞骨架与 TGFβ 信号转导的调控:探索它们之间的联系。
Biomolecules. 2021 Feb 23;11(2):336. doi: 10.3390/biom11020336.
5
Prognostic value of OCT4 in colorectal cancer: analysis using immunohistochemistry and bioinformatics validation.OCT4 在结直肠癌中的预后价值:免疫组织化学分析和生物信息学验证。
Biomark Med. 2020 Oct;14(15):1473-1484. doi: 10.2217/bmm-2020-0069. Epub 2020 Oct 14.
6
Relative Expression of SOX2 and OCT4 in Oral Squamous Cell Carcinoma and Oral Epithelial Dysplasia.SOX2和OCT4在口腔鳞状细胞癌及口腔上皮发育异常中的相对表达
Rep Biochem Mol Biol. 2020 Jul;9(2):171-179. doi: 10.29252/rbmb.9.2.171.
7
Prognostic Significance of ALDH1, Bmi1, and OCT4 Expression in Oral Epithelial Dysplasia and Oral Squamous Cell Carcinoma.ALDH1、Bmi1 和 OCT4 表达在口腔上皮异型增生和口腔鳞状细胞癌中的预后意义。
Cancer Control. 2020 Jan-Dec;27(1):1073274820904959. doi: 10.1177/1073274820904959.
8
Expression patterns and clinical significance of the potential cancer stem cell markers OCT4 and NANOG in colorectal cancer patients.潜在癌症干细胞标志物OCT4和NANOG在结直肠癌患者中的表达模式及临床意义
Mol Cell Oncol. 2020 Jul 14;7(5):1788366. doi: 10.1080/23723556.2020.1788366. eCollection 2020.
9
The Role and Specific Mechanism of OCT4 in Cancer Stem Cells: A Review.OCT4在癌症干细胞中的作用及具体机制:综述
Int J Stem Cells. 2020 Nov 30;13(3):312-325. doi: 10.15283/ijsc20097.
10
Mucoepidermoid carcinoma. An update and review of the literature.黏液表皮样癌。文献回顾与更新。
J Stomatol Oral Maxillofac Surg. 2020 Dec;121(6):713-720. doi: 10.1016/j.jormas.2020.06.003. Epub 2020 Jun 18.