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三阴性乳腺癌进展和转移中的上皮-间质转化指数

英文原题:Epithelial-Mesenchymal Transition Indexes in Triple-Negative Breast Cancer Progression and Metastases.

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Epithelial-Mesenchymal Transition Indexes in Triple-Negative Breast Cancer Progression and Metastases.

PubMed 2024/09/06(内容时间) Cureus

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中文摘要

背景 三阴性乳腺癌(TNBC)是一种高度侵袭性的乳腺癌亚型,其特征为缺乏雌激素受体和孕激素受体的表达,且不存在HER2蛋白过表达或基因扩增。TNBC在分子水平上如何变得如此具有侵袭性,目前尚未完全清楚。上皮-间充质转化(EMT)已被越来越多地认为在癌症进展和转移中发挥关键作用。

本研究旨在阐明TNBC进展与EMT相关标志物(包括vimentin、beta-catenin和E-cadherin)之间的联系。方法 采用严格的免疫组化分析,评估137例2018年至2024年间诊断的浸润性导管癌三阴性表型病例的原发肿瘤、肿瘤出芽和淋巴结转移(LNMs)中vimentin、beta-catenin和E-cadherin的表达。EMT指数在我们的工作中尤为重要,其为vimentin和beta-catenin表达之和除以E-cadherin表达。采用估计的Pearson相关性、多元线性回归和Kruskal-Wallis检验来确定EMT指数与肿瘤出芽和TIL(肿瘤浸润淋巴细胞)(TILs)的关系。结果 Vimentin在不同感兴趣区域之间高度相关,Pearson相关系数为0.90至0.92(p < 0.001)。E-cadherin与vimentin之间呈强负相关(r = -0.81至-0.89,p < 0.001),表明其在维持上皮表型中的作用。

肿瘤出芽、聚集或从原发肿瘤肿块脱落并侵入结缔组织的癌细胞簇的存在与EMT指数呈非常强的关联(r = 0.91,p < 0.001)。它的存在提示侵袭性疾病,并可能识别出可能受益于更积极监测或辅助治疗的高风险亚群。同样,TILs 与 EMT 指数呈负相关(r = -0.90,p < 0.001)。EMT 指数最显著的预测因子,即 vimentin,在回归分析中模型 R-squared 值为 1.000。结论 本研究揭示了 EMT 相关标志物在 TNBC 进展中的重要性,特别强调肿瘤出芽可能作为侵袭性疾病的预后指标。TILs 与 EMT 指数的负相关表明,有效的免疫反应可能拮抗 EMT 介导的肿瘤进展。这些结果提示,TNBC 中基于 EMT 的治疗应从多标志物角度设计,纳入多个标志物之间的相互作用,以优化预测和治疗。这些结果具有潜力为未来研究方向和有影响力的结局设定方向,并可能影响 TNBC 斗争中的临床效用。

展开英文摘要原文

Background Triple-negative breast cancer (TNBC) is a highly aggressive subtype of breast cancer characterized by the lack of expression of estrogen and progesterone receptors and the absence of HER2 protein overexpression or gene amplification. How TNBC becomes so aggressive at the molecular level is not yet fully understood. The epithelial-mesenchymal transition (EMT) has been increasingly recognized as playing a pivotal role in cancer progression and metastasis.

This study aimed to elucidate the connection between TNBC progression with EMT-related markers, including vimentin, beta-catenin, and E-cadherin. Methodology Rigorous immunohistochemical analysis was employed to assess the expression of vimentin, beta-catenin, and E-cadherin in primary tumors, tumor buds, and lymph node metastases (LNMs) from 137 cases with an invasive ductal carcinoma triple-negative phenotype diagnosed between 2018 and 2024. The EMT index, which was especially important in our work, is the sum of vimentin and beta-catenin expression divided by that of E-cadherin. Estimated Pearson correlation, multiple linear regression, and Kruskal-Wallis tests were used to determine the relationships of the EMT index with tumor buds and tumor-infiltrating lymphocytes (TILs). Results Vimentin highly correlated within separate regions of interest with Pearson correlation ranging from 0. 90 to 0. 92 (p < 0. 001). Strong negative correlations between E-cadherin and vimentin (r = -0. 81 to - 0. 89, p < 0. 001) showed its role in preserving the epithelial phenotype. The presence of tumor buds, aggregates, or clusters of cancer cells shed from the primary tumor mass invading the connective tissue showed very strong associations with the EMT index (r = 0.

91, p < 0. 001). Its presence is suggestive of aggressive disease and may identify a high-risk subpopulation that may benefit from more active surveillance or adjuvant treatment. Similarly, TILs correlated inversely with the EMT index (r = -0. 90, p < 0. 001). The most significant predictor of the EMT index, i. e. , vimentin, had a model R-squared value of 1. 000 in the regression analysis. Conclusions This study brings to light the importance of EMT-related markers in TNBC progression, with special emphasis on tumor buds as possible prognostic indicators for aggressive disease.

The negative correlation of TILs with the EMT index indicates that an effective immune response could antagonize EMT-mediated tumor progression. These results suggest that EMT-based treatments in TNBC should be designed from a multimarker perspective by including interactions among several markers to optimize predictions and therapeutics. The results hold the potential to set future research directions and actionable outcomes that could influence clinical utility in the battle against TNBC.

论文信息

作者
Kepuladze S、Burkadze G、Kokhreidze I
第一作者单位
Pathology and Oncology, Tbilisi State Medical University, Tbilisi, GEO.Georgia
通讯作者单位
Oncology, Tbilisi State Medical University, Tbilisi, GEO.Georgia
期刊
Cureus2024 Sep
原文标识
PubMed 39371729 · DOI 10.7759/cureus.68761