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Dual-positive CTCs in patients with advanced breast cancer show metastatic potential and prognostic value

医学 循环肿瘤细胞 恶性肿瘤 肿瘤科 转移 乳腺癌 内科学 转移性乳腺癌 队列 癌症 肺癌 生物标志物 CA15-3号 临床意义 远处转移 总体生存率 疾病 液体活检 癌细胞 癌症研究 比例危险模型 生存分析 基因型
作者
Carolina Reduzzi,E. Nicolo,Lorenzo Gerratana,Lauren L. Ozimski,Marco Silvestri,Youbin Zhang,David Scholten,Mara Serena Serafini,M. Manai,Paolo D’Amico,E. Molteni,Nadia Bayou,Brenno Pastò,Massimo Saini,A. A. Davis,Serena Di Cosimo,Vera Cappelletti,Huiping Liu,William J. Gradishar,Nicola Aceto
出处
期刊:Science Translational Medicine [American Association for the Advancement of Science]
卷期号:18 (840): eadw7698-eadw7698
标识
DOI:10.1126/scitranslmed.adw7698
摘要

Metastasis is the leading cause of death in patients with breast cancer (BC), but the mechanisms underlying metastasis formation are still poorly understood. Circulating tumor cells (CTCs) are considered the main seed of metastasis with demonstrated prognostic impact in patients with BC. They are conventionally identified as cells positive for epithelial markers and lacking leukocyte markers. Nonetheless, circulating cells expressing both markers [dual-positive cells (DPcells)] have been reported but poorly investigated. Here, we evaluated, in a cohort of 340 patients with advanced BC, the prognostic impact of DPcells, showing their association with worse survival, particularly in patients with less than five CTCs. Their prognostic value varied among BC subtypes, with greater relevance observed in triple-negative and HER2-positive BC. Moreover, by performing single-cell genomic profiling of DPcells isolated from patients, we detected genomic aberrations in 28 and 93% of analyzed DPcells and CTCs, respectively. In vivo, DPcells were detected only in the blood of immunocompetent but not immunodeficient mice and no differences in the lung metastatic colonization ability of DPcells versus control cancer cells were observed. Our findings highlight the importance of studying this overlooked subpopulation of CTCs as a prognostic biomarker in BC, which might be particularly important in specific BC subtypes. Moreover, our results support the malignancy and metastasis-forming capability of DPcells and underline the need for future studies better defining the origin of these cells.
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