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将肿瘤免疫浸润与无复发生存期乳腺癌患者的长寿增强联系起来。

Linking tumor immune infiltration to enhanced longevity in recurrence-free breast cancer.

作者信息

Angelats L, Paré L, Rubio-Perez C, Sanfeliu E, González A, Seguí E, Villacampa G, Marín-Aguilera M, Pernas S, Conte B, Albarrán-Fernández V, Martínez-Sáez O, Aguirre Á, Galván P, Fernandez-Martinez A, Cobo S, Rey M, Martínez-Romero A, Walbaum B, Schettini F, Vidal M, Buckingham W, Muñoz M, Adamo B, Agrawal Y, Guedan S, Pascual T, Agudo J, Grzelak M, Borcherding N, Heyn H, Vivancos A, Parker J S, Villagrasa P, Perou C M, Prat A, Brasó-Maristany F

机构信息

Translational Genomics and Targeted Therapies in Solid Tumors group, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain; Institute of Cancer and Blood Diseases, Hospital Clinic of Barcelona, Barcelona, Spain; Department of Medicine, University of Barcelona, Barcelona, Spain.

Reveal Genomics, Barcelona, Spain.

出版信息

ESMO Open. 2025 Jan;10(1):104109. doi: 10.1016/j.esmoop.2024.104109. Epub 2025 Jan 6.

Abstract

BACKGROUND

The infiltration of tumor-infiltrating B cells and plasma cells in early-stage breast cancer has been associated with a reduced risk of distant metastasis. However, the influence of B-cell tumor infiltration on overall patient survival remains unclear.

MATERIALS AND METHODS

This study explored the relationship between an antitumor immune response, measured by a 14-gene B-cell/immunoglobulin (IGG) signature, and mortality risk in 9638 breast cancer patients across three datasets. Associations with tumor subtype, stage, and age were examined. IGG was characterized using spatial GeoMx profiling and single-cell RNA sequencing, and its relationship with tertiary lymphoid structures (TLSs) was evaluated. The predictive value of each of the 14 IGG genes for B-cell receptor (BCR) and T-cell receptor (TCR) clonality and longevity was also assessed, along with its association with longevity in other cancer types.

RESULTS

High IGG signature expression was significantly associated with a 41%-47% reduction in death risk in breast cancer survivors (P < 0.001), regardless of age, tumor stage, or subtype. Similar associations were observed in other cancers, including melanoma. In breast cancer, the IGG signature was significantly linked to overall survival without relapse in patients aged 41-70 years at diagnosis. Additionally, IGG expression correlated with the presence of TLSs and higher B- and T-cell polyclonality. A specific subset of seven IGG genes strongly correlated with BCR and TCR clonality, with predictive power for identifying clonality and improved longevity, especially when combining two of these genes.

CONCLUSIONS

This study uncovers a significant link between immune gene expression in tumors and extended longevity in breast cancer survivors, even in the absence of recurrence. The IGG signature, particularly its key gene subset, emerges as a powerful marker of sustained antitumor immunity and overall patient fitness. These findings pave the way for personalized treatment strategies that enhance both survival and long-term health outcomes.

摘要

背景

早期乳腺癌中肿瘤浸润性B细胞和浆细胞的浸润与远处转移风险降低有关。然而,B细胞肿瘤浸润对患者总体生存的影响仍不清楚。

材料与方法

本研究通过一个14基因的B细胞/免疫球蛋白(IGG)特征来衡量抗肿瘤免疫反应,并探讨其与来自三个数据集的9638例乳腺癌患者死亡风险之间的关系。研究了其与肿瘤亚型、分期和年龄的相关性。使用空间GeoMx分析和单细胞RNA测序对IGG进行表征,并评估其与三级淋巴结构(TLS)的关系。还评估了14个IGG基因中每个基因对B细胞受体(BCR)和T细胞受体(TCR)克隆性及持久性的预测价值,以及其与其他癌症类型中持久性的关联。

结果

无论年龄、肿瘤分期或亚型如何,高IGG特征表达均与乳腺癌幸存者死亡风险显著降低41%-47%相关(P<0.001)。在包括黑色素瘤在内的其他癌症中也观察到了类似的关联。在乳腺癌中,IGG特征与诊断时年龄在41-70岁患者的无复发生存期显著相关。此外,IGG表达与TLS的存在以及更高的B细胞和T细胞多克隆性相关。七个IGG基因的特定子集与BCR和TCR克隆性密切相关,具有识别克隆性和改善持久性的预测能力,尤其是将其中两个基因结合使用时。

结论

本研究揭示了肿瘤中的免疫基因表达与乳腺癌幸存者延长生存期之间的显著联系,即使在无复发的情况下也是如此。IGG特征,尤其是其关键基因子集,成为持续抗肿瘤免疫和患者总体健康状况的有力标志物。这些发现为提高生存率和长期健康结局的个性化治疗策略铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4954/11758579/f9c199d658f0/gr1.jpg

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