KiSS1 suppresses metastasis in human ovarian cancer via inhibition of protein kinase C alpha

被引:128
|
作者
Jiang, Y
Berk, M
Singh, LS
Tan, HY
Yin, LH
Powell, CT
Xu, Y
机构
[1] Cleveland Clin Fdn, Lerner Res Inst, Dept Canc Biol, Cleveland, OH 44195 USA
[2] Cleveland Clin Fdn, Dept Gynecol & Obstet, Cleveland, OH 44195 USA
[3] Case Western Reserve Univ, Cleveland Clin, Lerner Coll Med, Dept Mol Med, Cleveland, OH 44106 USA
关键词
in vivo mouse model; KiSS1; lysophosphatidic acid (LPA); metastasis; ovarian cancer; protein kinase C (PKC);
D O I
10.1007/s10585-005-8186-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metastasis is a vital target for cancer treatment, since the majority of cancer patients die from metastatic, rather than the primary disease. KiSS1 has been identified as a metastasis suppressor gene in melanoma and breast carcinomas. We show here that KiSS1 is also a metastasis suppressor in human ovarian cancer. Overexpression of KiSS1 in ovarian cancer cells inhibits cell migration induced by serum or lysophosphatidic acid (LPA), and colonization in soft agar, but not cell proliferation, representing the characteristics of a metastasis suppressor gene. Furthermore, using an experimental metastatic mouse model, we show that expression of KiSS1 in SKOV3 ovarian cancer cells suppresses > 50% metastatic colonization in mice (P < 0.0001). We find that activating protein kinase C (PKC) reverses about 80% of the inhibited cell migration induced by KiSS1, while down-regulation of PKC alpha with shRNA restores KiSS1 effect, providing evidence that inhibiting PKC alpha may be an important mechanism of the effect of KiSS1. These results suggest that KiSS1 is a metastasis suppressor of ovarian cancer and may be a potential molecular target for the treatment.
引用
收藏
页码:369 / 376
页数:8
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