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Red Blood Cells Protein Profile Is Modified in Breast Cancer Patients.
Pereira-Veiga, Thais; Bravo, Susana; Gómez-Tato, Antonio; Yáñez-Gómez, Celso; Abuín, Carmen; Varela, Vanesa; Cueva, Juan; Palacios, Patricia; Dávila-Ibáñez, Ana B; Piñeiro, Roberto; Vilar, Ana; Chantada-Vázquez, María Del Pilar; López-López, Rafael; Costa, Clotilde.
Afiliação
  • Pereira-Veiga T; Roche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain.
  • Bravo S; Proteomic Unit, Instituto de Investigaciones Sanitarias-IDIS, Complejo Hospitalario Universitario de Santiago de Compostela (CHUS), Santiago de Compostela, Spain.
  • Gómez-Tato A; CITMAga, University of Santiago de Compostela (Campus Vida), Santiago de Compostela, Spain.
  • Yáñez-Gómez C; Roche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain.
  • Abuín C; Roche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain.
  • Varela V; Department of Oncology, University Hospital of Santiago de Compostela (SERGAS), Santiago de Compostela, Spain.
  • Cueva J; Department of Oncology, University Hospital of Santiago de Compostela (SERGAS), Santiago de Compostela, Spain.
  • Palacios P; Department of Oncology, University Hospital of Santiago de Compostela (SERGAS), Santiago de Compostela, Spain.
  • Dávila-Ibáñez AB; Roche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain; CIBERONC, Centro de Investigación Biomédica en Red Cáncer, Madrid, Spain.
  • Piñeiro R; Roche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain; CIBERONC, Centro de Investigación Biomédica en Red Cáncer, Madrid, Spain.
  • Vilar A; Department of Gynecology, University Hospital of Santiago de Compostela (SERGAS), Santiago de Compostela, Spain.
  • Chantada-Vázquez MDP; Proteomic Unit, Instituto de Investigaciones Sanitarias-IDIS, Complejo Hospitalario Universitario de Santiago de Compostela (CHUS), Santiago de Compostela, Spain.
  • López-López R; Roche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain; Department of Oncology, University Hospital of Santiago de Compostela (SERGAS), Santiago de Compostela, Spain; CIBERONC, Centro de Investig
  • Costa C; Roche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain; CIBERONC, Centro de Investigación Biomédica en Red Cáncer, Madrid, Spain. Electronic address: clotilde.costa.nogueira@sergas.es.
Mol Cell Proteomics ; 21(12): 100435, 2022 12.
Article em En | MEDLINE | ID: mdl-36519745
ABSTRACT
Metastasis is the primary cause of death for most breast cancer (BC) patients who succumb to the disease. During the hematogenous dissemination, circulating tumor cells interact with different blood components. Thus, there are microenvironmental and systemic processes contributing to cancer regulation. We have recently published that red blood cells (RBCs) that accompany circulating tumor cells have prognostic value in metastatic BC patients. RBC alterations are related to several diseases. Although the principal known role 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 BC patients from stages I to III and IV, compared with 33 cancer-free controls. In this work, we observed that RBCs from BC patients showed a different proteomic profile compared to cancer-free controls and between different tumor stages. The differential proteins were mainly related to extracellular components, proteasome, and metabolism. Embryonic hemoglobins, not expected in adults' RBCs, were detected in BC patients. Besides, lysosome-associated membrane glycoprotein 2 emerge as a new RBCs marker with diagnostic and prognostic potential for metastatic BC patients. Seemingly, RBCs are acquiring modifications in their proteomic composition that probably represents the systemic cancer disease, conditioned by the tumor microenvironment.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Células Neoplásicas Circulantes Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Células Neoplásicas Circulantes Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article