Transient Commensal Clonal Interactions Can Drive Tumor Metastasis
To interrogate functional heterogeneity and crosstalk between tumor cells, we generated clonal populations from a patient-derived ovarian clear cell carcinoma model which forms malignant ascites and solid peritoneal tumors upon intraperitoneal transplantation in mice. The clonal populations were eng...
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| Vydáno v: | bioRxiv |
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| Hlavní autoři: | , , , , , , , , , , , , , , , , , , |
| Médium: | Paper |
| Jazyk: | angličtina |
| Vydáno: |
Cold Spring Harbor
Cold Spring Harbor Laboratory Press
16.01.2020
Cold Spring Harbor Laboratory |
| Vydání: | 1.1 |
| Témata: | |
| ISSN: | 2692-8205, 2692-8205 |
| On-line přístup: | Získat plný text |
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| Shrnutí: | To interrogate functional heterogeneity and crosstalk between tumor cells, we generated clonal populations from a patient-derived ovarian clear cell carcinoma model which forms malignant ascites and solid peritoneal tumors upon intraperitoneal transplantation in mice. The clonal populations were engineered with secreted Gaussia luciferase to monitor tumor growth dynamics and tagged with a unique DNA barcode to track their fate in multiclonal mixtures during tumor progression. Only one clone, CL31, grew robustly, generating exclusively malignant ascites. However, multiclonal mixtures formed large solid peritoneal metastases, populated almost entirely by CL31, suggesting that transient cooperative interclonal interactions were sufficient to promote metastasis of CL31. CL31 uniquely harbored ERBB2 amplification, and its acquired metastatic trait was dependent on transient exposure to amphiregulin, which was exclusively secreted by non-tumorigenic clones. Amphiregulin enhanced CL31 mesothelial clearance, a prerequisite for metastasis. These findings demonstrate that transient, ostensibly innocuous tumor subpopulations can promote metastases via ″hit-and-run″ commensal interactions. |
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| Bibliografie: | SourceType-Working Papers-1 ObjectType-Working Paper/Pre-Print-1 content type line 50 |
| ISSN: | 2692-8205 2692-8205 |
| DOI: | 10.1101/2020.01.16.907071 |