Axl-Gas6 interaction counteracts E1A-mediated cell growth suppression and proapoptotic activity

Wei Ping Lee, Yong Liao, Dan Robinson, Hsing Jien Kung, Edison T. Liu, Mien Chie Hung

Research output: Contribution to journalArticle

52 Citations (Scopus)

Abstract

The adenovirus type 5 early region 1A gene (E1A) has previously been known as an immortalization oncogene because E1A is required for transforming oncogenes, such as ras and E1B, to transform cells in primary cultures. However, E1A has also been shown to downregulate the overexpression of the Her-2/neu oncogene, resulting in suppression of transformation and tumorigenesis induced by that oncogene. In addition, E1A is able to promote apoptosis induced by anticancer drugs, irradiation, and serum deprivation. Many tyrosine kinases, such as the epidermal growth factor receptor, Her- 2/Neu, Src, and Axl, are known to play a role in oncogenic signals in transformed cells. To study the mechanism underlying the E1A-mediated tumor- suppressing function, we exploited a modified tyrosine kinase profile assay (D. Robinson, F. Lee, T. Pretlow, and H.-J. Kung, Proc. Natl. Acad. Sci. USA 93:5958-5962, 1996) to identify potential tyrosine kinases regulated by E1A. Reverse transcription (RT)-PCR products were synthesized with two degenerate primers derived from the conserved motifs of various tyrosine kinases. A tyrosine kinase downregulated by E1A was identified by analyzing the AluI- digested RT-PCR products. We isolated the DNA fragment of interest and found that E1A negatively regulated the expression of the transforming receptor tyrosine kinase Axl at the transcriptional level. To study whether downregulation of the Axl receptor is involved in E1A-mediated growth suppression, we transfected axl cDNA into E1A-expressing cells (ipl-E1A) to establish cells that overexpressed Axl. The Axl ligand Gas6 triggered a greater mitogenic effect in these ip1-E1A-Ax1 cells than in ipl-E1A control cells and protected the Axl-expressing cells from serum deprivation-induced apoptosis. These results indicate that downregulation of the Ax1 receptor by E1A is involved in E1A-mediated growth suppression and E1A-induced apoptosis and thereby contributes to E1A's antitumor activities.

Original languageEnglish
Pages (from-to)8075-8082
Number of pages8
JournalMolecular and Cellular Biology
Volume19
Issue number12
DOIs
Publication statusPublished - Jan 1 1999
Externally publishedYes

Fingerprint

Protein-Tyrosine Kinases
Oncogenes
Down-Regulation
Growth
Apoptosis
Reverse Transcription
Polymerase Chain Reaction
Primary Cell Culture
Serum
Epidermal Growth Factor Receptor
Adenoviridae
Carcinogenesis
Complementary DNA
Ligands
DNA
Pharmaceutical Preparations
Genes
Neoplasms

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

Cite this

Axl-Gas6 interaction counteracts E1A-mediated cell growth suppression and proapoptotic activity. / Lee, Wei Ping; Liao, Yong; Robinson, Dan; Kung, Hsing Jien; Liu, Edison T.; Hung, Mien Chie.

In: Molecular and Cellular Biology, Vol. 19, No. 12, 01.01.1999, p. 8075-8082.

Research output: Contribution to journalArticle

Lee, Wei Ping ; Liao, Yong ; Robinson, Dan ; Kung, Hsing Jien ; Liu, Edison T. ; Hung, Mien Chie. / Axl-Gas6 interaction counteracts E1A-mediated cell growth suppression and proapoptotic activity. In: Molecular and Cellular Biology. 1999 ; Vol. 19, No. 12. pp. 8075-8082.
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