Heldin N E
Department of Genetics and Pathology, Rudbeck Laboratory, Uppsala University Hospital, SE-751 85 Uppsala, Sweden.
Biochem Biophys Res Commun. 2001 Jul 20;285(3):773-81. doi: 10.1006/bbrc.2001.5212.
The aim of the present study was to investigate the effect of bone morphogenetic protein (BMP-7) on thyroid carcinoma cell growth. Addition of BMP-7 inhibited the proliferation of four out of six human anaplastic thyroid carcinoma cell lines, observed as decreased incorporation of (3)H-thymidine and decreased cell number. The growth inhibitory effect was cell density-dependent; sparse cells were inhibited by BMP-7 whereas dense cells were not. Cell cycle analysis by flow cytometry showed an increased fraction of cells in the G1-phase and subsequent decrease in both S- and G2/M-phase after BMP-7 stimulation. Furthermore, BMP-7 caused an upregulation of the cyclin-dependent kinase inhibitors (CDKIs) p21 and p27, decreased activity of Cdk2 and Cdk6, and hypophosphorylation of the retinoblastoma protein (pRb). These findings suggest a growth inhibitory effect of BMP-7 on anaplastic thyroid carcinoma cells by inhibition of Cdk activity shifting the Rb protein to the hypophosphorylated state.
本研究的目的是探讨骨形态发生蛋白(BMP - 7)对甲状腺癌细胞生长的影响。添加BMP - 7可抑制六种人未分化甲状腺癌细胞系中的四种细胞系的增殖,表现为(3)H - 胸腺嘧啶核苷掺入减少和细胞数量减少。生长抑制作用呈细胞密度依赖性;稀疏细胞受到BMP - 7的抑制,而密集细胞则不受抑制。通过流式细胞术进行的细胞周期分析显示,BMP - 7刺激后,G1期细胞比例增加,随后S期和G2/M期细胞比例均下降。此外,BMP - 7导致细胞周期蛋白依赖性激酶抑制剂(CDKIs)p21和p27上调,Cdk2和Cdk6活性降低,视网膜母细胞瘤蛋白(pRb)发生低磷酸化。这些发现表明,BMP - 7通过抑制Cdk活性使Rb蛋白转变为低磷酸化状态,从而对未分化甲状腺癌细胞产生生长抑制作用。