Hung Tzong-Tyng, Wang Hong, Kingsley Elizabeth A, Risbridger Gail P, Russell Pamela J
Oncology Research Centre, Level 2, Clinical Sciences Building, Prince of Wales Hospital, Barker Street, Randwick, NSW 2031, Australia.
Cancer Lett. 2008 Jun 28;265(1):27-38. doi: 10.1016/j.canlet.2008.02.034. Epub 2008 May 13.
A human bladder cancer model of nine cell sublines derived from the BL17/2 cell line was used to evaluate genes related to disease progression. Molecular profiling of sublines that were non-tumorigenic and invasive in nude mice was performed and identified 1367 differentially-expressed genes. Quantitative real-time PCR analysis of six transforming growth factor-beta (TGF-beta) pathway genes using the entire panel of nine cell lines was performed. Bone morphogenetic protein-2 expression was significantly associated with in vivo tumorigenicity of the cell lines (p=0.0228, Mann-Whitney); inhibin-betaB was related to their invasiveness (p=0.0468, Mann-Whitney). Analysis of conditioned medium showed TGF-beta1 production to be significantly associated with the phenotype of the cell line. The study shows the possible involvement of the TGF-beta pathway in bladder cancer progression.
利用源自BL17/2细胞系的九个细胞亚系建立的人膀胱癌模型来评估与疾病进展相关的基因。对在裸鼠中无致瘤性和具有侵袭性的亚系进行了分子谱分析,鉴定出1367个差异表达基因。使用全部九个细胞系对六个转化生长因子-β(TGF-β)通路基因进行了定量实时PCR分析。骨形态发生蛋白-2的表达与细胞系的体内致瘤性显著相关(p=0.0228,曼-惠特尼检验);抑制素-βB与其侵袭性相关(p=0.0468,曼-惠特尼检验)。条件培养基分析表明,TGF-β1的产生与细胞系的表型显著相关。该研究表明TGF-β通路可能参与膀胱癌的进展。