Fibrinolytic activity of circulating microvesicles is associated with progression of breast cancer


Por: Valente-Acosta, Benjamin, Flores-Garcia, Mirthala, Gonzalez-Zarate, Georgina, Gerson-Cwilich, Raquel, Maldonado-Mendez, Marai, Juarez-Vega, Guillermo, Angles-Cano, Eduardo, de la Peña-Díaz A.

Publicada: 1 ene 2020
Resumen:
The fibrinolytic system plays an important role in breast cancer, favoring progression through extracellular-matrix degradation, angiogenesis, apoptosis and cellular proliferation. The expression of urokinase-type plasminogen activator (uPA) in breast cancer tissue is widely recognized as an unfavorable prognostic factor. However, fibrinolytic activity associated with uPA cannot be reliably measured in the blood because of the rapid inhibition of uPA by plasminogen activator inhibitor-1 (PAI-1). By contrast, circulating microvesicles (Mvs) in peripheral blood protect bound enzymes from inhibition. Mvs are extracellular vesicles, released from various types of cells, and their size fluctuates between 100 and 1,000 nm. Mvs carry DNA, RNA, miRNA, and proteins, thereby serving as a source of horizontal communication between cells. We investigated whether fibrinolytic activity on circulating Mvs reflects breast cancer progression. The study population consisted of 13 patients with breast cancer and 13 healthy women. The cancer patients included 4 patients in remission, 3 patients with locally advanced cancer, and 6 with metastatic disease. Mvs were isolated from peripheral blood, quantified by a protein concentration method, and their fibrinolytic potential was measured by their capacity to generate plasmin. Although the quantity of Mvs found in patients with cancer and healthy individuals was similar, plasmin generated on Mvs was twice the amount in patients with metastasis than in healthy women (P < 0.05), underlying the value of this distinctive parameter. The data suggest that in breast cancer patients, higher fibrinolytic activity of circulating Mvs could be related to progression and metastasis of breast cancer. © 2020 Tohoku University Medical Press.

Filiaciones:
Valente-Acosta, Benjamin:
 Departamento de Medicina Interna y Centro de Cáncer, The American British Cowdray Medical Center, Ciudad de México, Mexico

 Amer British Cowdray Med Ctr, Dept Med Interna, Mexico City, DF, Mexico

 Amer British Cowdray Med Ctr, Ctr Canc, Mexico City, DF, Mexico

Flores-Garcia, Mirthala:
 Departamento de Biología Molecular, Instituto Nacional de Cardiología Ignacio Chávez, Ciudad de México, Mexico

 Inst Nacl Cardiol Ignacio Chavez, Dept Biol Mol, Mexico City, DF, Mexico

Gonzalez-Zarate, Georgina:
 Laboratorio Clínico, Hospital General Dr. Fernando Quiroz, ISSSTE, Ciudad de México, Mexico

 ISSSTE, Hosp Gen Dr Fernando Quiroz, Lab Clin, Mexico City, DF, Mexico

Gerson-Cwilich, Raquel:
 Departamento de Medicina Interna y Centro de Cáncer, The American British Cowdray Medical Center, Ciudad de México, Mexico

 Amer British Cowdray Med Ctr, Dept Med Interna, Mexico City, DF, Mexico

 Amer British Cowdray Med Ctr, Ctr Canc, Mexico City, DF, Mexico

Maldonado-Mendez, Marai:
 Laboratorio de Trombosis y Fibrinolisis, Departamento de Farmacología, Facultad de Medicina, Universidad Nacional Autónoma de México, Ciudad de México, Mexico

 Univ Nacl Autonoma Mexico, Fac Med, Dept Farmacol, Lab Trombosis & Fibrinolisis, Mexico City, DF, Mexico

Juarez-Vega, Guillermo:
 Unidad de Citometría de Flujo, Red de Apoyo a la Investigación, Coordinación de Investigación Científica, Universidad Nacional Autónoma de México, Ciudad de México, Mexico

 Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Ciudad de México, Mexico

 Univ Nacl Autonoma Mexico, Coordinac Invest Cient, Red Apoyo Invest, Unidad Citometria Flujo, Mexico City, DF, Mexico

 Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Mexico City, DF, Mexico

Angles-Cano, Eduardo:
 Université de Paris, Innovative Therapies in Haemostasis, INSERM, Paris, France

 Univ Paris, Innovat Therapies Haemostasis, INSERM, Paris, France

de la Peña-Díaz A.:
 Departamento de Biología Molecular, Instituto Nacional de Cardiología Ignacio Chávez, Ciudad de México, Mexico

 Laboratorio de Trombosis y Fibrinolisis, Departamento de Farmacología, Facultad de Medicina, Universidad Nacional Autónoma de México, Ciudad de México, Mexico

 Departamento de Farmacología, Facultad de Medicina, Universidad Nacional Autónoma de México, Ciudad Universitaria, Edificio D, 1er piso, Ciudad de México, 04510, Mexico

Univ Nacl Autonoma Mexico, Dept Farmacol, Fac Med, Edificio D,l Er Piso,Ciudad Univ, Mexico City 04510, DF, Mexico
ISSN: 00408727
Editorial
TOHOKU UNIV MEDICAL PRESS, 2-1, SEIRYO-MACHI, AOBA-KU, SENDAI, MIYAGI 980-8575, JAPAN, Japón
Tipo de documento: Article
Volumen: 250 Número: 2
Páginas: 121-128
WOS Id: 000521099500005
ID de PubMed: 32115494

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