Modeling colorectal cancer progression reveals niche-dependent clonal selection

Colorectal cancer (CRC) is among the deadliest cancers worldwide, with metastasis being the main cause of patient mortality. During CRC progression the complex tumor ecosystem changes in its composition at virtually every stage. However, clonal dynamics and associated niche-dependencies at these sta...

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Hauptverfasser: Vaquero Siguero, Nuria (VerfasserIn) , Schleußner, Nikolai (VerfasserIn) , Volk, Julia (VerfasserIn) , Mastel, Manuel (VerfasserIn) , Meier, Jasmin (VerfasserIn) , Jackstadt, René-Filip (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 31 August 2022
In: Cancers
Year: 2022, Jahrgang: 14, Heft: 17, Pages: 1-19
ISSN:2072-6694
DOI:10.3390/cancers14174260
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.3390/cancers14174260
Verlag, lizenzpflichtig, Volltext: https://www.mdpi.com/2072-6694/14/17/4260
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Verfasserangaben:Nuria Vaquero-Siguero, Nikolai Schleussner, Julia Volk, Manuel Mastel, Jasmin Meier, Rene Jackstadt
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Zusammenfassung:Colorectal cancer (CRC) is among the deadliest cancers worldwide, with metastasis being the main cause of patient mortality. During CRC progression the complex tumor ecosystem changes in its composition at virtually every stage. However, clonal dynamics and associated niche-dependencies at these stages are unknown. Hence, it is of importance to utilize models that faithfully recapitulate human CRC to define its clonal dynamics. We used an optical barcoding approach in mouse-derived organoids (MDOs) that revealed niche-dependent clonal selection. Our findings highlight that clonal selection is controlled by a site-specific niche, which critically contributes to cancer heterogeneity and has implications for therapeutic intervention.
Beschreibung:Gesehen am 26.10.2022
Beschreibung:Online Resource
ISSN:2072-6694
DOI:10.3390/cancers14174260