bioRxiv · 10.1101/2022.12.09.519805
Propagated circulating tumor cells uncovers the rople of NFκB and COP1 in metastasis
Abstract
Circulating tumor cells (CTCs), a population of cancer cells that represents the seeds of metastatic nodules, are a promising model system for studying metastasis. However, expansion of patient-derived CTCs ex vivo is challenging and dependent on the collection of high numbers of CTCs, which are ultra-rare. Here, we report the development of a combined CTC and CTC-derived xenograft (CDX) platform for expanding and studying patient-derived CTCs from metastatic colon, lung, and pancreatic cancers. Propagated CTCs yielded a highly aggressive population of cells that could be used to routinely and robustly establish primary tumors and metastatic lesions in CDXs. Differential gene analysis of the resultant CTC models emphasized a role for NF-kB signaling as a pan-cancer signaling pathway involved in metastasis. Furthermore, metastatic CTCs were identified through a prospective 5-gene signature (BCAR1, COL1A1, IGSF3, RRAD, and TFPI2). Whole-exome sequencing of CDX models and metastases further identified mutations in constitutive photomorphogenesis protein 1 (COP1) as a potential driver of metastasis. These findings illustrate the utility of the combined patient-derived CTC model and provide a glimpse of the promise of CTCs in identifying drivers of cancer metastasis.
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Xiao, J., Sharma, U., Arab, A., Miglani, S., Bhalla, S., Suguru, S., Suter, R., Mukherji, R., Lippman, M. E., Pohlmann, P. R., Zeck, J., Marshall, J. L., Weinberg, B. A., He, A. R., Noel, M. S., Schlegel, R., Goodarzi, H., Agarwal, S.. 2022-12-11. Propagated circulating tumor cells uncovers the rople of NFκB and COP1 in metastasis. https://doi.org/10.1101/2022.12.09.519805
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