Profiling the downstream genes of tumor suppressor PTEN in lung cancer cells by complementary DNA microarray

T. M. Hong, P. C. Yang, K. Peck, J. J.W. Chen, S. C. Yang, Y. C. Chen, C. W. Wu

研究成果: Article同行評審

73 引文 斯高帕斯(Scopus)

摘要

The phosphatase and tensin homology deleted on chromosome 10 (PTEN) is a tumor suppressor gene with sequence homology to tyrosine phosphatases and the cytoskeletal proteins tensin and auxilin. PTEN has recently been shown to inhibit cell migration and the spreading and formation of focal adhesions. This study investigated the role of PTEN in carcinoma invasion in a lung-cancer cell line and examined the downstream genes regulated by PTEN. We have previously established a cell-line model in human lung adenocarcinoma with different invasive abilities and metastatic potentials. Examining PTEN gene expression in these cell lines, we found that a homozygous deletion in exon 5 is associated with high invasive ability. We then constructed stable constitutive and inducible wild-type PTEN-overexpressed transfectants in the highly invasive cell line CL1-5. We found that an overexpression of PTEN can inhibit invasion in lung cancer cells. To further explore the downstream genes regulated by PTEN, a high-density complementary DNA (cDNA) microarray technique was used to profile gene changes after PTEN overexpression. Our results indicate a panel of genes that can be modulated by PTEN. PTEN overexpression downregulated genes, including integrin α6, laminin β3, heparin-binding epidermal growth factor-like growth factor, urokinase-type plasminogen activator, myb protein B, Akt2, and some expressed sequence tag (EST) clones. In contrast, PTEN overexpression upregulated protein phosphatase 2A1B, ubiquitin protease (unph), secreted phosphoprotein 1, leukocyte elastase inhibitor, nuclear factor-κB, cyclic adenosine monophosphate response element binding protein, DNA ligase 1, heat shock protein 90, and some EST genes. Northern hybridization and flow cytometry analysis also confirmed that PTEN overexpression results in the reduced expression of the integrin α6 subunit. The results of this study indicate that PTEN overexpression may inhibit lung cancer invasion by downregulation of a panel of genes including integrin α6. The cDNA microarray technique may be an effective tool to study the downstream function of a tumor suppressor gene.

原文English
頁(從 - 到)355-363
頁數9
期刊American Journal of Respiratory Cell and Molecular Biology
23
發行號3
DOIs
出版狀態Published - 2000

All Science Journal Classification (ASJC) codes

  • 分子生物學
  • 肺和呼吸系統醫學
  • 臨床生物化學
  • 細胞生物學

指紋

深入研究「Profiling the downstream genes of tumor suppressor PTEN in lung cancer cells by complementary DNA microarray」主題。共同形成了獨特的指紋。

引用此