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间皮素(MSLN)在三阴性乳腺癌中高表达,并与细胞增殖增强和促炎性肿瘤微环境相关。

Mesothelin (MSLN) is Highly Expressed in Triple Negative Breast Cancer and is Associated with Enhanced Cell Proliferation and Proinflammatory Tumor Microenvironment.

作者信息

Hagerty Brendan L, Sato Takumi, Wu Rongrong, Ishikawa Takashi, Takabe Kazuaki

机构信息

Department of Surgical Oncology, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.

Department of Breast Surgery and Oncology, Tokyo Medical University, Tokyo, Japan.

出版信息

Ann Surg Oncol. 2025 Jun;32(6):4476-4486. doi: 10.1245/s10434-025-17117-y. Epub 2025 Mar 13.

Abstract

BACKGROUND

Mesothelin (MSLN), a cell surface glycoprotein, is commonly expressed in several cancers, including 40% of triple negative breast cancer (TNBC) cases. Although its cellular or physiologic functions remain unclear, MSLN has been leveraged as a target for molecular therapies. This study investigates MSLN's potential role in TNBC, the breast cancer (BC) subtype with poorest outcomes.

PATIENTS AND METHODS

The breast cancer (BC) cohorts from the Molecular Taxonomy of Breast Cancer International Consortium (METABRIC, n = 313), The Cancer Genome Atlas (TCGA, n = 160), and SCAN-B (n = 155) were used to obtain biological variables and gene expression data.

RESULTS

High MSLN expression was primarily observed in epithelial cells, and its expression was associated with reduced stromal adipocytes in the tumor microenvironment (TME), supporting its role as a TNBC surface marker. MSLN expression was also associated with the TNBC subtype and advanced N stages in BC. However, MSLN expression did not correlate with long-term survival outcomes, including overall survival (OS), disease-specific survival (DSS), or disease-free survival (DFS); nevertheless, it was still associated with favorable response to neoadjuvant chemotherapy (NAC). Indeed, MSLN-high tumors exhibited a proinflammatory microenvironment, higher cancer-testis antigen (CTA) scores, and increased immune cell activity, notably immature dendritic cells (iDCs) and M1 macrophages. Biologically, MSLN expression was linked to increased cellular proliferation, with gene set enrichment analysis (GSEA) showing enrichment in pathways related to rapid proliferation, such as G2M checkpoint and E2F targets.

CONCLUSIONS

MSLN-high TNBC is characterized by increased tumor grade, enhanced cell proliferation, and a proinflammatory microenvironment, showing better response to neoadjuvant chemotherapy without significant impact on long-term survival outcomes.

摘要

背景

间皮素(MSLN)是一种细胞表面糖蛋白,在多种癌症中普遍表达,包括40%的三阴性乳腺癌(TNBC)病例。尽管其细胞或生理功能尚不清楚,但MSLN已被用作分子治疗的靶点。本研究调查MSLN在TNBC(预后最差的乳腺癌亚型)中的潜在作用。

患者与方法

使用来自国际乳腺癌分子分类联盟(METABRIC,n = 313)、癌症基因组图谱(TCGA,n = 160)和SCAN-B(n = 155)的乳腺癌队列来获取生物学变量和基因表达数据。

结果

高MSLN表达主要见于上皮细胞,其表达与肿瘤微环境(TME)中基质脂肪细胞减少有关,支持其作为TNBC表面标志物的作用。MSLN表达还与TNBC亚型以及乳腺癌的晚期N分期相关。然而,MSLN表达与长期生存结果无关,包括总生存(OS)、疾病特异性生存(DSS)或无病生存(DFS);尽管如此,它仍与对新辅助化疗(NAC)的良好反应相关。事实上,高MSLN肿瘤表现出促炎微环境、更高的癌-睾丸抗原(CTA)评分以及免疫细胞活性增加,尤其是未成熟树突状细胞(iDCs)和M1巨噬细胞。在生物学上,MSLN表达与细胞增殖增加有关,基因集富集分析(GSEA)显示在与快速增殖相关的通路中富集,如G2M检查点和E2F靶点。

结论

高MSLN的TNBC的特征是肿瘤分级增加、细胞增殖增强和促炎微环境,对新辅助化疗表现出更好的反应,而对长期生存结果无显著影响。

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