Axl receptor tyrosine kinase expression in human lung cancer cell lines correlates with cellular adhesion

• Published in: European journal of cancer (1990) 2001-11, Vol.37 (17), p.2264-2274
• Main Authors: Wimmel, A, Glitz, D, Kraus, A, Roeder, J, Schuermann, M
• Format: Article
• Language: English
• Subjects: Axl protein; Axl Receptor Tyrosine Kinase; Biological and medical sciences; Blotting, Western; Carcinoma, Non-Small-Cell Lung - enzymology; Carcinoma, Non-Small-Cell Lung - metabolism; Carcinoma, Non-Small-Cell Lung - pathology; Carcinoma, Small Cell - enzymology; Carcinoma, Small Cell - metabolism; Carcinoma, Small Cell - pathology; Cell adhesion; Cell Adhesion - physiology; Cell Division - physiology; Gas6; Gene Expression; Humans; Intercellular Signaling Peptides and Proteins; Lung cancer; lung carcinoma; Lung Neoplasms - enzymology; Lung Neoplasms - metabolism; Lung Neoplasms - pathology; Medical sciences; Neoplasm Proteins - biosynthesis; Oncogene Proteins - metabolism; Pneumology; Protein Processing, Post-Translational; Proteins - genetics; Proteins - metabolism; Proto-Oncogene Proteins; Receptor Protein-Tyrosine Kinases - metabolism; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - genetics; RNA, Neoplasm - genetics; Tumor Cells, Cultured; Tumors of the respiratory system and mediastinum
• ISSN: 0959-8049; 1879-0852
• DOI: 10.1016/S0959-8049(01)00271-4

Axl is a receptor tyrosine kinase (RTK) with oncogenic potential and transforming activity. Since Axl bears structural similarities to cell adhesion molecules such as neural cell adhesion molecule (NCAM) (FNIII domains), it is thought that Axl might play a role in adhesion. In this study, we have analysed the expression of the Axl protein and its ligand, Gas6, in human lung cancer cell lines of different histological origin. Axl expression occurred in approximately 60% of non-small cell lung cancer (NSCLC) cell lines, which grow adherently, and in normal bronchial epithelial cells (NHBE), but not in cell lines of small cell lung cancer origin (SCLC), which grow in suspension. A number of SCLC sublines, which could be selected spontaneously or after oncogene transfection for adherent growth, all expressed Axl protein. Overexpression of Axl per se, however, did not induce any change in the adhesion phenotype. All Axl-expressing cell lines demonstrated a membrane-bound 140 kD form, as well as a soluble 85 kD form, detectable in supernatant, of Axl-RTK. Expression of the Axl ligand Gas6 was detected in approximately 80% of all cell lines investigated. We conclude from these data that loss of Axl expression is a feature of SCLC tumour cells. Axl expression appears to be a consequence of cellular adhesion and possibly influences differentiation in human lung cancers.