Populational equilibrium through exosome-mediated Wnt signaling in tumor progression of diffuse large B-cell lymphoma
Autor: | Christina Kiecke, Wolfram Klapper, Nina Diering, Gerald Wulf, Lennart Opitz, Bjoern Chapuy, Lorenz Trümper, Raphael Koch, Sabrina Becker, Vivek Venkataramani, Timo Hupfeld, Thiha Aung, Marlen Lahmann, Anna Cicholas, Martin Demant, Dirk Wenzel, Marita Ziepert, Annemarie Güntsch |
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Rok vydání: | 2014 |
Předmět: |
Immunology
Population Cell Count Biology Exosomes Biochemistry Exosome 03 medical and health sciences 0302 clinical medicine Side population medicine Tumor Cells Cultured Homeostasis Humans education Wnt Signaling Pathway 030304 developmental biology Cell Proliferation 0303 health sciences education.field_of_study Cell growth HEK 293 cells Wnt signaling pathway Cell Biology Hematology medicine.disease Cell biology Clone Cells Protein Transport HEK293 Cells Tumor progression 030220 oncology & carcinogenesis Disease Progression Neoplastic Stem Cells Lymphoma Large B-Cell Diffuse Diffuse large B-cell lymphoma |
Zdroj: | Blood |
ISSN: | 1528-0020 |
Popis: | Tumors are composed of phenotypically heterogeneous cell populations. The non-genomic mechanisms underlying transitions and interactions between cell populations are largely unknown. Here, we show that diffuse large B-cell lymphomas possess a self-organized infrastructure comprising side population (SP) and non-SP cells, where transitions between clonogenic states are modulated by exosome-mediated Wnt signaling. DNA methylation modulated SP-non-SP transitions and was correlated with the reciprocal expressions of Wnt signaling pathway agonist Wnt3a in SP cells and the antagonist secreted frizzled-related protein 4 in non-SP cells. Lymphoma SP cells exhibited autonomous clonogenicity and exported Wnt3a via exosomes to neighboring cells, thus modulating population equilibrium in the tumor. |
Databáze: | OpenAIRE |
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