Liu Chen, Chen Yaohui, Yu Xianjun, Jin Chen, Xu Jin, Long Jiang, Ni Quanxing, Fu Deliang, Jin Hong, Bai Chen
Pancreatic Disease Institute, Department of General Surgery, Huashan Hospital, Fudan University, Shanghai 200040, PR China.
BMC Cancer. 2008 Apr 29;8:121. doi: 10.1186/1471-2407-8-121.
Methyl-CpG binding domain protein 1 (MBD1), a suppressor of gene transcription, may be involved in inactivation of tumor suppressor genes during tumorigenesis. Over-expression of MBD1 has been reported in human pancreatic carcinomas.
In this study, we established a MBD1-knock-down pancreatic cancer cell line (BxPC-3) using stable RNA interference, to compare the proteomic changes between control and MBD1-knock-down cells using two-dimensional gel electrophoresis and mass spectrometry.
We identified five proteins that were up-regulated and nine proteins that were down-regulated. Most of the identified proteins are involved in tumorigenesis, some are prognostic biomarkers for human malignant tumors.
Our data suggest that these differential proteins may be associated with the function of MBD1, and provide some insight into the functional mechanism of MBD1 in the development of pancreatic cancer.
甲基化CpG结合域蛋白1(MBD1)是一种基因转录抑制因子,可能在肿瘤发生过程中参与肿瘤抑制基因的失活。已有报道称MBD1在人胰腺癌中过表达。
在本研究中,我们利用稳定的RNA干扰技术建立了MBD1敲低的胰腺癌细胞系(BxPC-3),通过二维凝胶电泳和质谱比较对照细胞和MBD1敲低细胞之间的蛋白质组变化。
我们鉴定出5种上调蛋白和9种下调蛋白。大多数鉴定出的蛋白都参与肿瘤发生,有些是人类恶性肿瘤的预后生物标志物。
我们的数据表明,这些差异蛋白可能与MBD1的功能相关,并为MBD1在胰腺癌发生发展中的功能机制提供了一些见解。