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

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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Publication Details

Journal
Science Translational Medicine
Published
2026-03-11
DOI
https://doi.org/10.1126/scitranslmed.adw7698
Primary Topic
Cancer Cells and Metastasis
Type
article
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article

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

Serena Di Cosimo, Youbin Zhang, Vera Cappelletti, Lauren L. Ozimski et al.
Science Translational Medicine
Cancer Cells and Metastasis
article

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

Serena Di Cosimo, Youbin Zhang, Vera Cappelletti, Lauren L. Ozimski, Huiping Liu, Mara Serena Serafini, Lorenzo Gerratana, Paolo D’Amico, David Scholten, Massimo Saini, Nicola Aceto, Nadia Bayou, M. Manai, A. A. Davis, E. Nicolo, E. Molteni, Carolina Reduzzi, William J. Gradishar, Brenno Pastò, Marco Silvestri, Massimo Cristofanilli
article en

Abstract

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.

Science Translational MedicineVol. 18(840)
Northwestern University (US), University of Udine (IT), Washington University in St. Louis (US), Cornell University (US), ETH Zurich (CH), Chan Zuckerberg Initiative (United States) (US), National Cancer Institute (UA), Institut Pasteur de Tunis (TN), Fondazione IRCCS Istituto Nazionale dei Tumori (IT), Weill Cornell Medicine (US), Chan Zuckerberg Biohub Chicago, École Polytechnique Fédérale de Lausanne (CH), Tunis El Manar University (TN)
Good health and well-being
Openalex Percentile: Top 24%
Cancer Cells and Metastasis
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