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An update on adrenocortical cell lines of human origin.
Endocrine 77, 432-437 (2022)
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DOI
PMC
Adrenocortical carcinoma (ACC) is a rare, heterogenous and highly malignant disease. Management of ACC is dependent on disease stage with complete surgical resection as the only potentially curative option. However, advanced, un-resectable, metastatic stages and also recurrences often require systemic treatments, which are unfortunately nowadays still unsatisfactory. The scarcity of preclinical models reflecting patient heterogeneities and furthermore drug-resistant phenotypes, has hampered the progress and development of new therapies in recent years. In this review, we provide an overview on the classical models and substantial progress which has been made over the last years in context of this aggressive disease.
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Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Review
ISSN (print) / ISBN
1355-008X
e-ISSN
1559-0100
Zeitschrift
Endocrine
Quellenangaben
Band: 77,
Heft: 3,
Seiten: 432-437
Verlag
Springer
Verlagsort
Totowa, NJ
Nichtpatentliteratur
Publikationen
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute for Pancreatic Beta Cell Research (IPI)
Förderungen
University of Zurich