The canine prostate cancer cell line CHP-1 shows over-expression of the co-chaperone small glutamine-rich tetratricopeptide repeat-containing protein

被引:11
作者
Azakami, D. [1 ]
Nakahira, R. [2 ]
Kato, Y. [1 ]
Michishita, M. [2 ]
Kobayashi, M. [3 ,4 ]
Onozawa, E. [1 ]
Bonkobara, M. [3 ]
Kobayashi, M. [3 ,4 ]
Takahashi, K. [2 ]
Watanabe, M. [5 ]
Ishioka, K. [1 ]
Sako, T. [1 ]
Ochiai, K. [1 ]
Omi, T. [1 ]
机构
[1] Nippon Vet & Life Sci Univ, Sch Vet Nursing & Technol, Fac Vet Sci, Tokyo 1808602, Japan
[2] Nippon Vet & Life Sci Univ, Dept Vet Pathol, Fac Vet Sci, Tokyo, Japan
[3] Nippon Vet & Life Sci Univ, Dept Vet Clin Pathol, Fac Vet Sci, Tokyo, Japan
[4] Nippon Vet & Life Sci Univ, Dept Reprod, Fac Vet Sci, Tokyo, Japan
[5] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Urol, Okayama, Japan
关键词
androgen receptor signalling; canine; prostate cancer; small glutamine-rich tetratricopeptide repeat-containing protein; ANDROGEN RECEPTOR; SGTA; BINDING; DOMAIN;
D O I
10.1111/vco.12199
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Although androgen therapy resistance and poor clinical outcomes are seen in most canine prostate cancer cases, there are only a few tools for analysing canine prostate cancer by using a cell biological approach. Therefore, to evaluate androgen-independent neoplastic cell growth, a new canine prostate cancer cell line (CHP-1) was established in this study. CHP-1 over-expressed the co-chaperone small glutamine-rich tetratricopeptide repeat-containing protein (SGTA), which is over-expressed in human androgen-independent prostate cancer. The CHP-1 xenograft also showed SGTA over-expression. Although CHP-1 shows poor androgen receptor (AR) signalling upon dihydrotestosterone stimulation, forced expression of AR enabled evaluation of AR signalling. Taken together, these results suggest that CHP-1 will be a useful model for investigating the pathogenesis of androgen-dependent and androgen-independent canine prostate cancer.
引用
收藏
页码:557 / 562
页数:6
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