Patient-Derived Organoids of Cholangiocarcinoma

Christopher Maier(German Cancer Research Center), Lei Zhu(German Cancer Research Center), Lahiri Kanth Nanduri(University Hospital Carl Gustav Carus), Daniel Kühn(University Hospital Carl Gustav Carus), Susan Kochall(University Hospital Carl Gustav Carus), May-Linn Thepkaysone(University Hospital Carl Gustav Carus), Doreen William(German Cancer Research Center), Konrad Grützmann(German Cancer Research Center), Barbara Klink(German Cancer Research Center), Johannes Betge(German Cancer Research Center), Jürgen Weitz(University Hospital Carl Gustav Carus), Nuh N. Rahbari(Heidelberg University), Christoph Reißfelder(Heidelberg University), Sebastian Schölch(German Cancer Research Center)
International Journal of Molecular Sciences
August 12, 2021
Cited by 59Open Access
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Abstract

Cholangiocarcinoma (CC) is an aggressive malignancy with an inferior prognosis due to limited systemic treatment options. As preclinical models such as CC cell lines are extremely rare, this manuscript reports a protocol of cholangiocarcinoma patient-derived organoid culture as well as a protocol for the transition of 3D organoid lines to 2D cell lines. Tissue samples of non-cancer bile duct and cholangiocarcinoma were obtained during surgical resection. Organoid lines were generated following a standardized protocol. 2D cell lines were generated from established organoid lines following a novel protocol. Subcutaneous and orthotopic patient-derived xenografts were generated from CC organoid lines, histologically examined, and treated using standard CC protocols. Therapeutic responses of organoids and 2D cell lines were examined using standard CC agents. Next-generation exome and RNA sequencing was performed on primary tumors and CC organoid lines. Patient-derived organoids closely recapitulated the original features of the primary tumors on multiple levels. Treatment experiments demonstrated that patient-derived organoids of cholangiocarcinoma and organoid-derived xenografts can be used for the evaluation of novel treatments and may therefore be used in personalized oncology approaches. In summary, this study establishes cholangiocarcinoma organoids and organoid-derived cell lines, thus expanding translational research resources of cholangiocarcinoma.


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