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A novel co-culture model of human prostate epithelial and stromal cells for androgenic and antiandrogenic screening.
Li, Hui; Madnick, Samantha; Zhao, He; Hall, Susan; Amin, Ali; Dent, Matthew P; Boekelheide, Kim.
Afiliação
  • Li H; Center for Drug Safety Evaluation and Research of Zhejiang University, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China; Department of Pathology and Laboratory Medicine, Brown University, Providence, RI, USA. Electronic address: hui_li@zju.edu.cn.
  • Madnick S; Department of Pathology and Laboratory Medicine, Brown University, Providence, RI, USA.
  • Zhao H; Center for Drug Safety Evaluation and Research of Zhejiang University, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China.
  • Hall S; Department of Pathology and Laboratory Medicine, Brown University, Providence, RI, USA.
  • Amin A; Department of Pathology and Laboratory Medicine, Brown University, Providence, RI, USA.
  • Dent MP; Safety and Environmental Assurance Centre, Unilever, Colworth Science Park, Bedfordshire MK44 1LQ, UK.
  • Boekelheide K; Department of Pathology and Laboratory Medicine, Brown University, Providence, RI, USA. Electronic address: Kim_Boekelheide@brown.edu.
Toxicol In Vitro ; 91: 105624, 2023 Sep.
Article em En | MEDLINE | ID: mdl-37230229
ABSTRACT
The risk assessment of endocrine-disrupting chemicals (EDCs) greatly relies on in vitro screening. A 3-dimensional (3D) in vitro prostate model that can reflect physiologically-relevant prostate epithelial and stromal crosstalk can significantly advance the current androgen assessment. This study built a prostate epithelial and stromal co-culture microtissue model with BHPrE and BHPrS cells in scaffold-free hydrogels. The optimal 3D co-culture condition was defined, and responses of the microtissue to androgen (dihydrotestosterone, DHT) and anti-androgen (flutamide) exposure were characterized using molecular and image profiling techniques. The co-culture prostate microtissue maintained a stable structure for up to seven days and presented molecular and morphological features of the early developmental stage of the human prostate. The cytokeratin 5/6 (CK5/6) and cytokeratin 18 (CK18) immunohistochemical staining indicated epithelial heterogeneity and differentiation in these microtissues. The prostate-related gene expression profiling did not efficiently differentiate androgen and anti-androgen exposure. However, a cluster of distinctive 3D image features was identified and could be applied in the androgenic and anti-androgenic effect prediction. Overall, the current study established a co-culture prostate model that provided an alternative strategy for (anti-)androgenic EDC safety assessment and highlighted the potential and advantage of utilizing image features to predict endpoints in chemical screening.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Próstata / Androgênios Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Humans / Male Idioma: En Revista: Toxicol In Vitro Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Próstata / Androgênios Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Humans / Male Idioma: En Revista: Toxicol In Vitro Ano de publicação: 2023 Tipo de documento: Article