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Red blood cells protein profile is modified in breast cancer patients

Thais Pereira-Veiga, Susana Bravo, View ORCID ProfileAntonio Gómez-Tato, Celso Yáñez-Gómez, Carmen Abuín, Vanesa Varela, Juan Cueva, Patricia Palacios, Ana B. Dávila-Ibáñez, Roberto Piñeiro, Ana Vilar, María del Pilar Chantada-Vázquez, Rafael López-López, View ORCID ProfileClotilde Costa
doi: https://doi.org/10.1101/2022.01.04.474889
Thais Pereira-Veiga
1Roche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela (IDIS), Travesía da Choupana s/n, 15706 Santiago de Compostela, Spain
2Department of Tumor Biology, Center of Experimental Medicine, University Medical Center Hamburg-Eppendorf, 20246, Hamburg, Germany
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Susana Bravo
3Proteomic Unit, Instituto de Investigaciones Sanitarias-IDIS, Complejo Hospitalario Universitario de Santiago de Compostela (CHUS), 15706 Santiago de Compostela, Spain
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Antonio Gómez-Tato
4CITMAga, University of Santiago de Compostela (Campus Vida), 15782 Santiago de Compostela, Spain
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  • ORCID record for Antonio Gómez-Tato
Celso Yáñez-Gómez
1Roche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela (IDIS), Travesía da Choupana s/n, 15706 Santiago de Compostela, Spain
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Carmen Abuín
1Roche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela (IDIS), Travesía da Choupana s/n, 15706 Santiago de Compostela, Spain
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Vanesa Varela
5Department of Oncology, University Hospital of Santiago de Compostela (SERGAS), 15706 Santiago de Compostela, Spain
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Juan Cueva
5Department of Oncology, University Hospital of Santiago de Compostela (SERGAS), 15706 Santiago de Compostela, Spain
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Patricia Palacios
5Department of Oncology, University Hospital of Santiago de Compostela (SERGAS), 15706 Santiago de Compostela, Spain
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Ana B. Dávila-Ibáñez
1Roche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela (IDIS), Travesía da Choupana s/n, 15706 Santiago de Compostela, Spain
6CIBERONC, Centro de Investigación Biomédica en Red Cáncer, 28029 Madrid, Spain
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Roberto Piñeiro
1Roche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela (IDIS), Travesía da Choupana s/n, 15706 Santiago de Compostela, Spain
6CIBERONC, Centro de Investigación Biomédica en Red Cáncer, 28029 Madrid, Spain
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Ana Vilar
7Department of Gynecology, University Hospital of Santiago de Compostela (SERGAS), Spain
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María del Pilar Chantada-Vázquez
3Proteomic Unit, Instituto de Investigaciones Sanitarias-IDIS, Complejo Hospitalario Universitario de Santiago de Compostela (CHUS), 15706 Santiago de Compostela, Spain
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Rafael López-López
1Roche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela (IDIS), Travesía da Choupana s/n, 15706 Santiago de Compostela, Spain
5Department of Oncology, University Hospital of Santiago de Compostela (SERGAS), 15706 Santiago de Compostela, Spain
6CIBERONC, Centro de Investigación Biomédica en Red Cáncer, 28029 Madrid, Spain
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  • For correspondence: clotilde.costa.nogueira@sergas.es Rafael.lopez.lopez@sergas.es
Clotilde Costa
1Roche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela (IDIS), Travesía da Choupana s/n, 15706 Santiago de Compostela, Spain
6CIBERONC, Centro de Investigación Biomédica en Red Cáncer, 28029 Madrid, Spain
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  • ORCID record for Clotilde Costa
  • For correspondence: clotilde.costa.nogueira@sergas.es Rafael.lopez.lopez@sergas.es
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Abstract

Metastasis is the primary cause of death for most breast cancer patients who succumb to the disease. During the haematogenous dissemination, circulating tumor cells interact with different blood components. Thus, there are micro-environmental and systemic processes contributing to cancer regulation. We have published that Red Blood Cells (RBCs) that accompany circulating tumor cells have prognostic value in metastatic breast cancer patients. Although the principal known role of RBCs is gas transport, it has been recently assigned additional functions as regulatory cells on circulation. Hence, to explore their potential contribution to tumor progression, we characterized the proteomic composition of RBCs from 53 breast cancer patients, compared with 33 healthy donors. RBCs from breast cancer patients showed a different proteomic profile compared to healthy donors. The differential proteins were mainly related to extracellular components, proteasome, and metabolism. Besides, LAMP2 emerge as a new RBCs marker with diagnostic and prognostic potential for metastatic patients. Seemingly, RBCs are acquiring modifications in their proteomic composition that probably represents the systemic cancer disease, conditioned by the tumor microenvironment.

  • Abbreviations
    CTCs
    circulating tumor cells
    DTCs
    disseminated tumor cells
    RBCs
    red blood cells
    BC
    breast cancer
    HD
    healthy donor
    HB
    haemoglobin
    EE
    extramedullary erythropoiesis
    MS
    mass spectrometry
    PFS
    progression-free survival
    OS
    overall survival
    M0
    non-metastatic
    M1
    metastatic
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    Posted January 06, 2022.
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    Red blood cells protein profile is modified in breast cancer patients
    Thais Pereira-Veiga, Susana Bravo, Antonio Gómez-Tato, Celso Yáñez-Gómez, Carmen Abuín, Vanesa Varela, Juan Cueva, Patricia Palacios, Ana B. Dávila-Ibáñez, Roberto Piñeiro, Ana Vilar, María del Pilar Chantada-Vázquez, Rafael López-López, Clotilde Costa
    bioRxiv 2022.01.04.474889; doi: https://doi.org/10.1101/2022.01.04.474889
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    Red blood cells protein profile is modified in breast cancer patients
    Thais Pereira-Veiga, Susana Bravo, Antonio Gómez-Tato, Celso Yáñez-Gómez, Carmen Abuín, Vanesa Varela, Juan Cueva, Patricia Palacios, Ana B. Dávila-Ibáñez, Roberto Piñeiro, Ana Vilar, María del Pilar Chantada-Vázquez, Rafael López-López, Clotilde Costa
    bioRxiv 2022.01.04.474889; doi: https://doi.org/10.1101/2022.01.04.474889

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