Propagation of human prostate tissue from induced pluripotent stem cells
Abstract Primary culture of human prostate organoids and patient‐derived xenografts is inefficient and has limited access to clinical tissues. This hampers their use for translational study to identify new treatments. To overcome this, we established a complementary approach where rapidly proliferat...
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Online Access: | https://doi.org/10.1002/sctm.19-0286 |
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doaj-1a016c78ab2e4635979543ad1a0a990f2020-11-25T03:55:58ZengWileyStem Cells Translational Medicine2157-65642157-65802020-07-019773474510.1002/sctm.19-0286Propagation of human prostate tissue from induced pluripotent stem cellsAnastasia C. Hepburn0Emma L. Curry1Mohammad Moad2Rebecca E. Steele3Omar E. Franco4Laura Wilson5Parmveer Singh6Adriana Buskin7Susan E. Crawford8Luke Gaughan9Ian G. Mills10Simon W. Hayward11Craig N. Robson12Rakesh Heer13Translational and Clinical Research Institute, Newcastle University Centre for Cancer Newcastle University Newcastle upon Tyne UKTranslational and Clinical Research Institute, Newcastle University Centre for Cancer Newcastle University Newcastle upon Tyne UKTranslational and Clinical Research Institute, Newcastle University Centre for Cancer Newcastle University Newcastle upon Tyne UKProstate Cancer UK/Movember Centre of Excellence for Prostate Cancer, Centre for Cancer Research and Cell Biology Queen's University of Belfast Belfast UKDepartment of Surgery NorthShore University HealthSystem Evanston Illinois USATranslational and Clinical Research Institute, Newcastle University Centre for Cancer Newcastle University Newcastle upon Tyne UKTranslational and Clinical Research Institute, Newcastle University Centre for Cancer Newcastle University Newcastle upon Tyne UKTranslational and Clinical Research Institute, Newcastle University Centre for Cancer Newcastle University Newcastle upon Tyne UKDepartment of Surgery NorthShore University HealthSystem Evanston Illinois USATranslational and Clinical Research Institute, Newcastle University Centre for Cancer Newcastle University Newcastle upon Tyne UKProstate Cancer UK/Movember Centre of Excellence for Prostate Cancer, Centre for Cancer Research and Cell Biology Queen's University of Belfast Belfast UKDepartment of Surgery NorthShore University HealthSystem Evanston Illinois USATranslational and Clinical Research Institute, Newcastle University Centre for Cancer Newcastle University Newcastle upon Tyne UKTranslational and Clinical Research Institute, Newcastle University Centre for Cancer Newcastle University Newcastle upon Tyne UKAbstract Primary culture of human prostate organoids and patient‐derived xenografts is inefficient and has limited access to clinical tissues. This hampers their use for translational study to identify new treatments. To overcome this, we established a complementary approach where rapidly proliferating and easily handled induced pluripotent stem cells enabled the generation of human prostate tissue in vivo and in vitro. By using a coculture technique with inductive urogenital sinus mesenchyme, we comprehensively recapitulated in situ 3D prostate histology, and overcame limitations in the primary culture of human prostate stem, luminal and neuroendocrine cells, as well as the stromal microenvironment. This model now unlocks new opportunities to undertake translational studies of benign and malignant prostate disease.https://doi.org/10.1002/sctm.19-0286androgen receptordifferentiationinduced pluripotent stem cellsorganoidsprostateprostate cancer |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Anastasia C. Hepburn Emma L. Curry Mohammad Moad Rebecca E. Steele Omar E. Franco Laura Wilson Parmveer Singh Adriana Buskin Susan E. Crawford Luke Gaughan Ian G. Mills Simon W. Hayward Craig N. Robson Rakesh Heer |
spellingShingle |
Anastasia C. Hepburn Emma L. Curry Mohammad Moad Rebecca E. Steele Omar E. Franco Laura Wilson Parmveer Singh Adriana Buskin Susan E. Crawford Luke Gaughan Ian G. Mills Simon W. Hayward Craig N. Robson Rakesh Heer Propagation of human prostate tissue from induced pluripotent stem cells Stem Cells Translational Medicine androgen receptor differentiation induced pluripotent stem cells organoids prostate prostate cancer |
author_facet |
Anastasia C. Hepburn Emma L. Curry Mohammad Moad Rebecca E. Steele Omar E. Franco Laura Wilson Parmveer Singh Adriana Buskin Susan E. Crawford Luke Gaughan Ian G. Mills Simon W. Hayward Craig N. Robson Rakesh Heer |
author_sort |
Anastasia C. Hepburn |
title |
Propagation of human prostate tissue from induced pluripotent stem cells |
title_short |
Propagation of human prostate tissue from induced pluripotent stem cells |
title_full |
Propagation of human prostate tissue from induced pluripotent stem cells |
title_fullStr |
Propagation of human prostate tissue from induced pluripotent stem cells |
title_full_unstemmed |
Propagation of human prostate tissue from induced pluripotent stem cells |
title_sort |
propagation of human prostate tissue from induced pluripotent stem cells |
publisher |
Wiley |
series |
Stem Cells Translational Medicine |
issn |
2157-6564 2157-6580 |
publishDate |
2020-07-01 |
description |
Abstract Primary culture of human prostate organoids and patient‐derived xenografts is inefficient and has limited access to clinical tissues. This hampers their use for translational study to identify new treatments. To overcome this, we established a complementary approach where rapidly proliferating and easily handled induced pluripotent stem cells enabled the generation of human prostate tissue in vivo and in vitro. By using a coculture technique with inductive urogenital sinus mesenchyme, we comprehensively recapitulated in situ 3D prostate histology, and overcame limitations in the primary culture of human prostate stem, luminal and neuroendocrine cells, as well as the stromal microenvironment. This model now unlocks new opportunities to undertake translational studies of benign and malignant prostate disease. |
topic |
androgen receptor differentiation induced pluripotent stem cells organoids prostate prostate cancer |
url |
https://doi.org/10.1002/sctm.19-0286 |
work_keys_str_mv |
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