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Spatiotemporal regulation of clonogenicity in colorectal cancer xenografts

Cancer evolution is predominantly studied by focusing on differences in the genetic characteristics of malignant cells within tumors. However, the spatiotemporal dynamics of clonal outgrowth that underlie evolutionary trajectories remain largely unresolved. Here, we sought to unravel the clonal dyna...

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Autores principales: van der Heijden, Maartje, Miedema, Daniël M., Waclaw, Bartlomiej, Veenstra, Veronique L., Lecca, Maria C., Nijman, Lisanne E., van Dijk, Erik, van Neerven, Sanne M., Lodestijn, Sophie C., Lenos, Kristiaan J., de Groot, Nina E., Prasetyanti, Pramudita R., Arricibita Varea, Andrea, Winton, Douglas J., Medema, Jan Paul, Morrissey, Edward, Ylstra, Bauke, Nowak, Martin A., Bijlsma, Maarten F., Vermeulen, Louis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6442578/
https://www.ncbi.nlm.nih.gov/pubmed/30850544
http://dx.doi.org/10.1073/pnas.1813417116
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author van der Heijden, Maartje
Miedema, Daniël M.
Waclaw, Bartlomiej
Veenstra, Veronique L.
Lecca, Maria C.
Nijman, Lisanne E.
van Dijk, Erik
van Neerven, Sanne M.
Lodestijn, Sophie C.
Lenos, Kristiaan J.
de Groot, Nina E.
Prasetyanti, Pramudita R.
Arricibita Varea, Andrea
Winton, Douglas J.
Medema, Jan Paul
Morrissey, Edward
Ylstra, Bauke
Nowak, Martin A.
Bijlsma, Maarten F.
Vermeulen, Louis
author_facet van der Heijden, Maartje
Miedema, Daniël M.
Waclaw, Bartlomiej
Veenstra, Veronique L.
Lecca, Maria C.
Nijman, Lisanne E.
van Dijk, Erik
van Neerven, Sanne M.
Lodestijn, Sophie C.
Lenos, Kristiaan J.
de Groot, Nina E.
Prasetyanti, Pramudita R.
Arricibita Varea, Andrea
Winton, Douglas J.
Medema, Jan Paul
Morrissey, Edward
Ylstra, Bauke
Nowak, Martin A.
Bijlsma, Maarten F.
Vermeulen, Louis
author_sort van der Heijden, Maartje
collection PubMed
description Cancer evolution is predominantly studied by focusing on differences in the genetic characteristics of malignant cells within tumors. However, the spatiotemporal dynamics of clonal outgrowth that underlie evolutionary trajectories remain largely unresolved. Here, we sought to unravel the clonal dynamics of colorectal cancer (CRC) expansion in space and time by using a color-based clonal tracing method. This method involves lentiviral red-green-blue (RGB) marking of cell populations, which enabled us to track individual cells and their clonal outgrowth during tumor initiation and growth in a xenograft model. We found that clonal expansion largely depends on the location of a clone, as small clones reside in the center and large clones mostly drive tumor growth at the border. These dynamics are recapitulated in a computational model, which confirms that the clone position within a tumor rather than cell-intrinsic features, is crucial for clonal outgrowth. We also found that no significant clonal loss occurs during tumor growth and clonal dispersal is limited in most models. Our results imply that, in addition to molecular features of clones such as (epi-)genetic differences between cells, clone location and the geometry of tumor growth are crucial for clonal expansion. Our findings suggest that either microenvironmental signals on the tumor border or differences in physical properties within the tumor, are major contributors to explain heterogeneous clonal expansion. Thus, this study provides further insights into the dynamics of solid tumor growth and progression, as well as the origins of tumor cell heterogeneity in a relevant model system.
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spelling pubmed-64425782019-04-05 Spatiotemporal regulation of clonogenicity in colorectal cancer xenografts van der Heijden, Maartje Miedema, Daniël M. Waclaw, Bartlomiej Veenstra, Veronique L. Lecca, Maria C. Nijman, Lisanne E. van Dijk, Erik van Neerven, Sanne M. Lodestijn, Sophie C. Lenos, Kristiaan J. de Groot, Nina E. Prasetyanti, Pramudita R. Arricibita Varea, Andrea Winton, Douglas J. Medema, Jan Paul Morrissey, Edward Ylstra, Bauke Nowak, Martin A. Bijlsma, Maarten F. Vermeulen, Louis Proc Natl Acad Sci U S A Biological Sciences Cancer evolution is predominantly studied by focusing on differences in the genetic characteristics of malignant cells within tumors. However, the spatiotemporal dynamics of clonal outgrowth that underlie evolutionary trajectories remain largely unresolved. Here, we sought to unravel the clonal dynamics of colorectal cancer (CRC) expansion in space and time by using a color-based clonal tracing method. This method involves lentiviral red-green-blue (RGB) marking of cell populations, which enabled us to track individual cells and their clonal outgrowth during tumor initiation and growth in a xenograft model. We found that clonal expansion largely depends on the location of a clone, as small clones reside in the center and large clones mostly drive tumor growth at the border. These dynamics are recapitulated in a computational model, which confirms that the clone position within a tumor rather than cell-intrinsic features, is crucial for clonal outgrowth. We also found that no significant clonal loss occurs during tumor growth and clonal dispersal is limited in most models. Our results imply that, in addition to molecular features of clones such as (epi-)genetic differences between cells, clone location and the geometry of tumor growth are crucial for clonal expansion. Our findings suggest that either microenvironmental signals on the tumor border or differences in physical properties within the tumor, are major contributors to explain heterogeneous clonal expansion. Thus, this study provides further insights into the dynamics of solid tumor growth and progression, as well as the origins of tumor cell heterogeneity in a relevant model system. National Academy of Sciences 2019-03-26 2019-03-08 /pmc/articles/PMC6442578/ /pubmed/30850544 http://dx.doi.org/10.1073/pnas.1813417116 Text en Copyright © 2019 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
van der Heijden, Maartje
Miedema, Daniël M.
Waclaw, Bartlomiej
Veenstra, Veronique L.
Lecca, Maria C.
Nijman, Lisanne E.
van Dijk, Erik
van Neerven, Sanne M.
Lodestijn, Sophie C.
Lenos, Kristiaan J.
de Groot, Nina E.
Prasetyanti, Pramudita R.
Arricibita Varea, Andrea
Winton, Douglas J.
Medema, Jan Paul
Morrissey, Edward
Ylstra, Bauke
Nowak, Martin A.
Bijlsma, Maarten F.
Vermeulen, Louis
Spatiotemporal regulation of clonogenicity in colorectal cancer xenografts
title Spatiotemporal regulation of clonogenicity in colorectal cancer xenografts
title_full Spatiotemporal regulation of clonogenicity in colorectal cancer xenografts
title_fullStr Spatiotemporal regulation of clonogenicity in colorectal cancer xenografts
title_full_unstemmed Spatiotemporal regulation of clonogenicity in colorectal cancer xenografts
title_short Spatiotemporal regulation of clonogenicity in colorectal cancer xenografts
title_sort spatiotemporal regulation of clonogenicity in colorectal cancer xenografts
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6442578/
https://www.ncbi.nlm.nih.gov/pubmed/30850544
http://dx.doi.org/10.1073/pnas.1813417116
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