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S100A4 的低甲基化诱导表达增加了喉鳞状细胞癌的侵袭性。

Hypomethylation-induced expression of S100A4 increases the invasiveness of laryngeal squamous cell carcinoma.

机构信息

Department of Medical Genetics, China Medical University, Shenyang 110001, PR China.

出版信息

Oncol Rep. 2010 Apr;23(4):1101-7.

Abstract

The present study aimed to identify genes related to 5AZA-CdR in laryngeal squamous cell carcinoma (LSCC) and to investigate the role of S100A4 in the development and aggression of LSCC. Differentially expressed proteins were identified in Hep-2 cells treated with 5AZA-CdR by two-dimensional gel electrophoresis combined with MALDI-TOF-MS. mRNA, protein levels and DNA methylation status of S100A4 were assessed by RT-PCR, Western blotting and methylation-specific PCR, respectively. The invasiveness of Hep-2 cells transfected by siRNA S100A4 was determined by transwell migration assay. Protein profiles from Hep-2 cells treated with 5AZA-CdR were obtained, and several differentially expressed proteins such as S100 calcium-binding protein A4 (S100A4) were identified. Results of RT-PCR and Western blotting revealed that both mRNA and protein levels of S100A4 were significantly higher in the metastatic lymph nodes than those in paired adjacent normal laryngeal (PANL) or tumor tissues. The DNA methylation status displayed significant differences between the LSCC and the PANL tissues. The expression level of S100A4 decreased in Hep-2 cells undergoing RNA interference of S100A4. The number of cells which crossed the basement membrane filter was significantly lower in the RNAi S100A4 group when compared with the number in the control group. The abnormal expression of S100A4 identified in Hep-2 cells treated with an inhibitor of DNA methyltransferase appeared to result from the aberrant DNA methylation status of S100A4. The abnormal expression of S100A4 altered the invasiveness of LSCC.

摘要

本研究旨在鉴定与 5AZA-CdR 相关的基因,并探讨 S100A4 在喉鳞状细胞癌(LSCC)发生和侵袭中的作用。通过二维凝胶电泳结合 MALDI-TOF-MS 鉴定用 5AZA-CdR 处理的 Hep-2 细胞中的差异表达蛋白。通过 RT-PCR、Western blot 和甲基化特异性 PCR 分别评估 S100A4 的 mRNA、蛋白水平和 DNA 甲基化状态。通过 Transwell 迁移实验测定转染 siRNA S100A4 的 Hep-2 细胞的侵袭性。从用 5AZA-CdR 处理的 Hep-2 细胞中获得蛋白图谱,并鉴定出几种差异表达的蛋白质,如 S100 钙结合蛋白 A4(S100A4)。RT-PCR 和 Western blot 的结果显示,转移淋巴结中 S100A4 的 mRNA 和蛋白水平均明显高于配对的相邻正常喉(PANL)或肿瘤组织。LSCC 和 PANL 组织之间的 DNA 甲基化状态存在显著差异。在 S100A4 进行 RNA 干扰的 Hep-2 细胞中,S100A4 的表达水平降低。与对照组相比,RNAi S100A4 组穿过基底膜过滤器的细胞数量明显减少。在用 DNA 甲基转移酶抑制剂处理的 Hep-2 细胞中发现 S100A4 的异常表达似乎是由于 S100A4 的异常 DNA 甲基化状态所致。S100A4 的异常表达改变了 LSCC 的侵袭性。

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