An update on adrenocortical cell lines of human origin

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 system...

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Main Authors: Sigala, Sandra, Rossini, Elisa, Abate, Andrea, Tamburello, Mariangela, Bornstein, Stefan R., Hantel, Constanze
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Article
Language:English
Published: 2022
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Online Access:https://hdl.handle.net/10356/163849
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1638492023-03-05T16:52:43Z An update on adrenocortical cell lines of human origin Sigala, Sandra Rossini, Elisa Abate, Andrea Tamburello, Mariangela Bornstein, Stefan R. Hantel, Constanze Lee Kong Chian School of Medicine (LKCMedicine) Science::Medicine Adrenal Cortex Carcinoma Adrenal Cortex Tumor 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. Published version Open access funding provided by University of Zurich. 2022-12-20T02:15:02Z 2022-12-20T02:15:02Z 2022 Journal Article Sigala, S., Rossini, E., Abate, A., Tamburello, M., Bornstein, S. R. & Hantel, C. (2022). An update on adrenocortical cell lines of human origin. Endocrine, 77(3), 432-437. https://dx.doi.org/10.1007/s12020-022-03112-w 1355-008X https://hdl.handle.net/10356/163849 10.1007/s12020-022-03112-w 35764904 2-s2.0-85133088196 3 77 432 437 en Endocrine © The Author(s) 2022. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons. org/licenses/by/4.0/. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Medicine
Adrenal Cortex Carcinoma
Adrenal Cortex Tumor
spellingShingle Science::Medicine
Adrenal Cortex Carcinoma
Adrenal Cortex Tumor
Sigala, Sandra
Rossini, Elisa
Abate, Andrea
Tamburello, Mariangela
Bornstein, Stefan R.
Hantel, Constanze
An update on adrenocortical cell lines of human origin
description 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.
author2 Lee Kong Chian School of Medicine (LKCMedicine)
author_facet Lee Kong Chian School of Medicine (LKCMedicine)
Sigala, Sandra
Rossini, Elisa
Abate, Andrea
Tamburello, Mariangela
Bornstein, Stefan R.
Hantel, Constanze
format Article
author Sigala, Sandra
Rossini, Elisa
Abate, Andrea
Tamburello, Mariangela
Bornstein, Stefan R.
Hantel, Constanze
author_sort Sigala, Sandra
title An update on adrenocortical cell lines of human origin
title_short An update on adrenocortical cell lines of human origin
title_full An update on adrenocortical cell lines of human origin
title_fullStr An update on adrenocortical cell lines of human origin
title_full_unstemmed An update on adrenocortical cell lines of human origin
title_sort update on adrenocortical cell lines of human origin
publishDate 2022
url https://hdl.handle.net/10356/163849
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