BM18: A novel androgen-dependent human prostate cancer xenograft model derived from a bone metastasis

被引:37
作者
McCulloch, DR
Opeskin, K
Thompson, EW
Williams, ED
机构
[1] Univ Melbourne, Bernard O Brien Inst Microsurg, Fitzroy, Vic 3065, Australia
[2] Univ Melbourne, Dept Surg, Fitzroy, Vic 3065, Australia
[3] Univ Melbourne, Dept Pathol, Fitzroy, Vic 3065, Australia
[4] St Vincents Hosp, Dept Pathol Anat, Fitzroy, Vic 3065, Australia
关键词
prostate cancer; xenograft; prostate specific antigen; androgen; androgen receptor; androgen-dependent;
D O I
10.1002/pros.20255
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
BACKGROUND. Androgen-dependent prostate cancer (PrCa) xenograft models are required to study PrCa biology in the clinically relevant in vivo environment. METHODS. Human PrCa tissue from a femoral bone metastasis biopsy (BM18) was grown and passaged subcutaneously through male severe combined immune-deficient (SCID) mice. Human mitochondria (hMt), prostate specific antigen (PSA), androgen receptor (AR), cytokeratin-18 (CK-18), pan-cytokeratin, and high molecular weight-cytokeratin (HMW-CK) were assessed using immunohistochemistry (IHC). Surgical castration was performed to examine androgen-dependence. Serum was collected pre- and post-castration for monitoring of PSA levels. RESULTS. BM18 stained positively for hMt, PSA, AR, CK-18, pan keratin, and negatively for HMW-CK, consistent with the staining observed in the original patient material. Androgen-deprivation induced tumor regression in 10/10 castrated male SCID mice. Serum PSA levels positively correlated with BM18 tumor size. CONCLUSIONS. BM18 expresses PSA and AR, and rapidly regresses in response to androgen withdrawal. This provides a new clinically significant PrCa model for the study of androgen-dependent growth.
引用
收藏
页码:35 / 43
页数:9
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