A tissue graft model of DNA damage response in the normal and malignant human prostate

Taija M. Af Hällström, Hongjuan Zhao, Junqiang Tian, Ville Rantanen, Stephen W. Reese, Rosalie Nolley, Marikki Laiho, Donna M. Peehl

Research output: Contribution to journalArticle

Abstract

Purpose DNA damage responses are relevant to prostate cancer initiation, progression and treatment. Few models of the normal and malignant human prostate that maintain stromal-epithelial interactions in vivo exist in which to study DNA damage responses. We evaluated the feasibility of maintaining tissue slice grafts at subcutaneous vs subrenal capsular sites in RAG2 -/-γC-/- mice to study the DNA damage responses of normal and malignant glands. Materials and Methods We compared the take rate and histology of tissue slice grafts from fresh, precision cut surgical specimens that were maintained for 1 to 4 weeks in subcutaneous vs subrenal capsular sites. Induction of γH2AX, p53, ATM and apoptosis was evaluated as a measure of the DNA damage response after irradiation. Results The take rate of subcutaneous tissue slice grafts was higher than typically reported but lower than at the subrenal capsular site. Subcutaneous tissue slice grafts frequently showed basal cell hyperplasia, squamous metaplasia and cystic atrophy, and cancer did not survive. In contrast, normal and malignant histology was well maintained in subrenal capsular tissue slice grafts. Regardless of implantation site the induction of γH2AX and ATM occurred in tissue slice graft epithelium 1 hour after irradiation and decreased to basal level by 24 hours, indicating DNA damage recognition and repair. As observed previously in prostatic ex vivo models, p53 was not activated. Notably, tumor but not normal cells responded to irradiation by undergoing apoptosis. Conclusions To our knowledge this is the first study of DNA damage responses in a patient derived prostate tissue graft model. The subrenal capsular site of RAG2 -/-γC-/- mice optimally maintains normal and malignant histology and function, permitting novel studies of DNA damage responses in a physiological context.

Original languageEnglish (US)
Pages (from-to)842-849
Number of pages8
JournalJournal of Urology
Volume191
Issue number3
DOIs
StatePublished - Mar 2014

Fingerprint

DNA Damage
Prostate
Transplants
Histology
Subcutaneous Tissue
Apoptosis
Metaplasia
DNA Repair
Atrophy
Hyperplasia
Neoplasms
Prostatic Neoplasms
Epithelium
Epithelial Cells

Keywords

  • DNA damage
  • H2AFX protein
  • human
  • prostate
  • prostatic neoplasms
  • transplants

ASJC Scopus subject areas

  • Urology

Cite this

Af Hällström, T. M., Zhao, H., Tian, J., Rantanen, V., Reese, S. W., Nolley, R., ... Peehl, D. M. (2014). A tissue graft model of DNA damage response in the normal and malignant human prostate. Journal of Urology, 191(3), 842-849. https://doi.org/10.1016/j.juro.2013.09.007

A tissue graft model of DNA damage response in the normal and malignant human prostate. / Af Hällström, Taija M.; Zhao, Hongjuan; Tian, Junqiang; Rantanen, Ville; Reese, Stephen W.; Nolley, Rosalie; Laiho, Marikki; Peehl, Donna M.

In: Journal of Urology, Vol. 191, No. 3, 03.2014, p. 842-849.

Research output: Contribution to journalArticle

Af Hällström, TM, Zhao, H, Tian, J, Rantanen, V, Reese, SW, Nolley, R, Laiho, M & Peehl, DM 2014, 'A tissue graft model of DNA damage response in the normal and malignant human prostate', Journal of Urology, vol. 191, no. 3, pp. 842-849. https://doi.org/10.1016/j.juro.2013.09.007
Af Hällström TM, Zhao H, Tian J, Rantanen V, Reese SW, Nolley R et al. A tissue graft model of DNA damage response in the normal and malignant human prostate. Journal of Urology. 2014 Mar;191(3):842-849. https://doi.org/10.1016/j.juro.2013.09.007
Af Hällström, Taija M. ; Zhao, Hongjuan ; Tian, Junqiang ; Rantanen, Ville ; Reese, Stephen W. ; Nolley, Rosalie ; Laiho, Marikki ; Peehl, Donna M. / A tissue graft model of DNA damage response in the normal and malignant human prostate. In: Journal of Urology. 2014 ; Vol. 191, No. 3. pp. 842-849.
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AU - Laiho, Marikki

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N2 - Purpose DNA damage responses are relevant to prostate cancer initiation, progression and treatment. Few models of the normal and malignant human prostate that maintain stromal-epithelial interactions in vivo exist in which to study DNA damage responses. We evaluated the feasibility of maintaining tissue slice grafts at subcutaneous vs subrenal capsular sites in RAG2 -/-γC-/- mice to study the DNA damage responses of normal and malignant glands. Materials and Methods We compared the take rate and histology of tissue slice grafts from fresh, precision cut surgical specimens that were maintained for 1 to 4 weeks in subcutaneous vs subrenal capsular sites. Induction of γH2AX, p53, ATM and apoptosis was evaluated as a measure of the DNA damage response after irradiation. Results The take rate of subcutaneous tissue slice grafts was higher than typically reported but lower than at the subrenal capsular site. Subcutaneous tissue slice grafts frequently showed basal cell hyperplasia, squamous metaplasia and cystic atrophy, and cancer did not survive. In contrast, normal and malignant histology was well maintained in subrenal capsular tissue slice grafts. Regardless of implantation site the induction of γH2AX and ATM occurred in tissue slice graft epithelium 1 hour after irradiation and decreased to basal level by 24 hours, indicating DNA damage recognition and repair. As observed previously in prostatic ex vivo models, p53 was not activated. Notably, tumor but not normal cells responded to irradiation by undergoing apoptosis. Conclusions To our knowledge this is the first study of DNA damage responses in a patient derived prostate tissue graft model. The subrenal capsular site of RAG2 -/-γC-/- mice optimally maintains normal and malignant histology and function, permitting novel studies of DNA damage responses in a physiological context.

AB - Purpose DNA damage responses are relevant to prostate cancer initiation, progression and treatment. Few models of the normal and malignant human prostate that maintain stromal-epithelial interactions in vivo exist in which to study DNA damage responses. We evaluated the feasibility of maintaining tissue slice grafts at subcutaneous vs subrenal capsular sites in RAG2 -/-γC-/- mice to study the DNA damage responses of normal and malignant glands. Materials and Methods We compared the take rate and histology of tissue slice grafts from fresh, precision cut surgical specimens that were maintained for 1 to 4 weeks in subcutaneous vs subrenal capsular sites. Induction of γH2AX, p53, ATM and apoptosis was evaluated as a measure of the DNA damage response after irradiation. Results The take rate of subcutaneous tissue slice grafts was higher than typically reported but lower than at the subrenal capsular site. Subcutaneous tissue slice grafts frequently showed basal cell hyperplasia, squamous metaplasia and cystic atrophy, and cancer did not survive. In contrast, normal and malignant histology was well maintained in subrenal capsular tissue slice grafts. Regardless of implantation site the induction of γH2AX and ATM occurred in tissue slice graft epithelium 1 hour after irradiation and decreased to basal level by 24 hours, indicating DNA damage recognition and repair. As observed previously in prostatic ex vivo models, p53 was not activated. Notably, tumor but not normal cells responded to irradiation by undergoing apoptosis. Conclusions To our knowledge this is the first study of DNA damage responses in a patient derived prostate tissue graft model. The subrenal capsular site of RAG2 -/-γC-/- mice optimally maintains normal and malignant histology and function, permitting novel studies of DNA damage responses in a physiological context.

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