Proteomic landscape of decellularized breast carcinomas identifies C-type lectin domain family 3 member A as a driver of cancer aggressiveness

An extracellular matrix (ECM) gene expression pattern (ECM3) distinguished truly aggressive grade III breast carcinomas (BCs). Here, we examined the biomechanical characteristics of the ECM in human BCs to identify the molecules that mediate the aggressiveness of ECM3/grade III (E3G3) tumors. By shotgun proteomics of decellularized human BCs, we found a significant enrichment in proteins involved in tumor-ECM interaction in E3G3 tumors. These tumors were characterized by high dense collagen deposition, a fibrillary cytoskeleton network and the highest stiffness. CLEC3A, a secreted C-type lectin domain family 3 member, was found unique of E3G3 tumors and was validated to be more expressed in these tumors by immunohistochemistry in 2 human BC cohorts, associating significantly with worse prognosis. Ectopic CLEC3A overexpression in MDA-MB-231, MDA-MB-361, and MDA-MB-468 BC cells increased intracellular mediators of tumor adhesion to the ECM, actin-stress fibers and YAP activation, and tumor migration. Accordingly, levels of the YAP/TAZ gene signature were higher in CLEC3A-positive ECM3-enriched tumors and correlated with tumor stiffness. These results implicate CLEC3A in mediating the ability of E3G3 BCs to sense cues in the surrounding ECM, accelerating tumor progression.

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Publication Details

Journal
npj Breast Cancer
Published
2025-06-06
DOI
https://doi.org/10.1038/s41523-025-00769-0
Citations
2
Primary Topic
Cell Adhesion Molecules Research
Type
article
Field-Weighted Citation Impact
3.24

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article

Proteomic landscape of decellularized breast carcinomas identifies C-type lectin domain family 3 member A as a driver of cancer aggressiveness

Sabina Pozzi, Lucia Sfondrini, Marco Sandri, Giovanni Vozzi et al.
2 citations
npj Breast Cancer
Cell Adhesion Molecules Research
3.24
article

Proteomic landscape of decellularized breast carcinomas identifies C-type lectin domain family 3 member A as a driver of cancer aggressiveness

Sabina Pozzi, Lucia Sfondrini, Marco Sandri, Giovanni Vozzi, Serenella M. Pupa, Viola Regondi, Ewelina Lorenc, Cesare Valenti, Marta Giussani, Valeria Cancila, Alessandro Podestà, Tiziana Triulzi, Elisa Maffioli, Valeria Arlotta, Elda Tagliabue, Francesca Bianchi, Gabriella Tedeschi, M. T. Varricchio
article en
2 citations

Abstract

An extracellular matrix (ECM) gene expression pattern (ECM3) distinguished truly aggressive grade III breast carcinomas (BCs). Here, we examined the biomechanical characteristics of the ECM in human BCs to identify the molecules that mediate the aggressiveness of ECM3/grade III (E3G3) tumors. By shotgun proteomics of decellularized human BCs, we found a significant enrichment in proteins involved in tumor-ECM interaction in E3G3 tumors. These tumors were characterized by high dense collagen deposition, a fibrillary cytoskeleton network and the highest stiffness. CLEC3A, a secreted C-type lectin domain family 3 member, was found unique of E3G3 tumors and was validated to be more expressed in these tumors by immunohistochemistry in 2 human BC cohorts, associating significantly with worse prognosis. Ectopic CLEC3A overexpression in MDA-MB-231, MDA-MB-361, and MDA-MB-468 BC cells increased intracellular mediators of tumor adhesion to the ECM, actin-stress fibers and YAP activation, and tumor migration. Accordingly, levels of the YAP/TAZ gene signature were higher in CLEC3A-positive ECM3-enriched tumors and correlated with tumor stiffness. These results implicate CLEC3A in mediating the ability of E3G3 BCs to sense cues in the surrounding ECM, accelerating tumor progression.

npj Breast CancerVol. 11(1)
University of Pisa (IT), Piaggio (Italy) (IT), University of Milan (IT), IRCCS Policlinico San Donato (IT), Fondazione IRCCS Istituto Nazionale dei Tumori (IT), University of Palermo (IT)
Ministero della Salute, Associazione Italiana per la Ricerca sul Cancro, Fondazione Italiana per la Ricerca sul Cancro
Good health and well-being
Openalex Percentile: Top 10%
Cell Adhesion Molecules Research
3.24
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