Tsui Ke-Hung, Chang Phei-Lang, Feng Tsui-Hsia, Chung Li-Chuan, Hsu Shu-Yuan, Juang Horng-Heng
Department of Urology, Chang Gung Memorial Hospital, Kwei-Shan, Tao-Yuan, Taiwan, ROC.
Anticancer Res. 2008 Jul-Aug;28(4A):1977-83.
The precise mechanisms of metastasis in prostatic cancer are still unknown. A subculture cell line (PC-J) was isolated from the metastasis human prostate cell line PC-3. In vitro cell proliferation, wound healing and invasion assays revealed that tumorigenesis and metastasis differed between PC-3 and PC-J cells. Eight weeks after nude mice were prostate-injected with PC-J and PC-3 cells, the PC-3 group had low tumor volume and exhibited metastasis whereas the PC-J group had high tumor volume and no metastasis. Subsequent RT-PCR and immunoblot assays indicated that matriptase was the putative metastatic gene. Overexpression of bikunin significantly reduced the gene expression of matriptase, which attenuated in vitro cell invasion in the PC-3 cells. In vitro and xenograft animal models indicated different metastatic characteristics between PC-3 and PC-J cells, suggesting that matriptase plays an important role in the metastasis of prostate cancer.
前列腺癌转移的确切机制仍不清楚。从转移性人前列腺癌细胞系PC-3中分离出一种传代细胞系(PC-J)。体外细胞增殖、伤口愈合和侵袭试验表明,PC-3和PC-J细胞之间的肿瘤发生和转移情况不同。将PC-J和PC-3细胞注射到裸鼠前列腺八周后,PC-3组肿瘤体积小且出现转移,而PC-J组肿瘤体积大且无转移。随后的逆转录聚合酶链反应(RT-PCR)和免疫印迹分析表明,matriptase是假定的转移基因。比库宁的过表达显著降低了matriptase的基因表达,这减弱了PC-3细胞的体外细胞侵袭。体外和异种移植动物模型表明PC-3和PC-J细胞之间具有不同的转移特征,提示matriptase在前列腺癌转移中起重要作用。