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...

Full description

Bibliographic Details
Main Authors: 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
Format: Article
Language:English
Published: Wiley 2020-07-01
Series:Stem Cells Translational Medicine
Subjects:
Online Access:https://doi.org/10.1002/sctm.19-0286
id doaj-1a016c78ab2e4635979543ad1a0a990f
record_format Article
spelling 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 AT anastasiachepburn propagationofhumanprostatetissuefrominducedpluripotentstemcells
AT emmalcurry propagationofhumanprostatetissuefrominducedpluripotentstemcells
AT mohammadmoad propagationofhumanprostatetissuefrominducedpluripotentstemcells
AT rebeccaesteele propagationofhumanprostatetissuefrominducedpluripotentstemcells
AT omarefranco propagationofhumanprostatetissuefrominducedpluripotentstemcells
AT laurawilson propagationofhumanprostatetissuefrominducedpluripotentstemcells
AT parmveersingh propagationofhumanprostatetissuefrominducedpluripotentstemcells
AT adrianabuskin propagationofhumanprostatetissuefrominducedpluripotentstemcells
AT susanecrawford propagationofhumanprostatetissuefrominducedpluripotentstemcells
AT lukegaughan propagationofhumanprostatetissuefrominducedpluripotentstemcells
AT iangmills propagationofhumanprostatetissuefrominducedpluripotentstemcells
AT simonwhayward propagationofhumanprostatetissuefrominducedpluripotentstemcells
AT craignrobson propagationofhumanprostatetissuefrominducedpluripotentstemcells
AT rakeshheer propagationofhumanprostatetissuefrominducedpluripotentstemcells
_version_ 1724467080003059712