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PMID: 9095173 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Progression of metastatic human prostate cancer to androgen independence in immunodeficient SCID mice.

Nature medicine ·Vol. 3 ·No. 4 ·1997-04-00 ·Pages 402-8

Klein KA, Reiter RE, Redula J, Moradi H, Zhu XL, Brothman AR, Lamb DJ, Marcelli M, Belldegrun A, Witte ON, Sawyers CL

Abstract

Prostate cancer mortality results from metastasis to bone and hormone-independent tumor growth. Models to study these progressive changes are lacking. Here we describe the propagation of advanced human prostate cancer by direct transfer of surgical samples from patients into immune-deficient male SCID mice. Explants from six of eight patients formed prostate tumors and two showed unique cytogenetic, biologic and molecular features that were retained through six or more passages. One grew in an androgen-independent fashion, whereas the second formed tumors that regressed following castration then regrew. Micrometastatic disease was detected in the hematopoietic tissues of half of the recipient mice. Thus selected specimens of advanced human prostate cancer can be propagated in SCID mice in a manner that recapitulates the clinical transition from androgen-sensitive to androgen-independent growth, accompanied by micrometastasis.

MeSH Terms
Androgens/metabolism Animals Humans Male Mice Mice, SCID Neoplasm Metastasis Neoplasm Staging Neoplasm Transplantation/methods Prostatic Neoplasms/metabolism,pathology,secondary Transplantation, Heterologous/methods
Chemicals
Androgens
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Klein K A
Department of Medicine, UCLA School of Medicine 90095-1678, USA.
Reiter R E
Redula J
Moradi H
Zhu X L
Brothman A R
Lamb D J
Marcelli M
Belldegrun A
Witte O N
Sawyers C L
Article Info
Journal
Nature medicine
Abbr.
Nat Med
ISSN
1078-8956
Published
1997-04-00
Pages
402-8
Language
English
Region
United States
NLM ID
9502015
Subset
IM
Grants
NCI NIH HHS · R01 CA 68615 · United States
NCI NIH HHS · R01-CA46269 · United States
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