Genomic and functional analysis identifies CRKL as an oncogene amplified in lung cancer.

Abstract

DNA amplifications, leading to the overexpression of oncogenes, are a cardinal feature of lung cancer and directly contribute to its pathogenesis. To uncover such novel alterations, we performed an array-based comparative genomic hybridization survey of 128 non-small-cell lung cancer cell lines and tumors. Prominent among our findings, we identified recurrent high-level amplification at cytoband 22q11.21 in 3% of lung cancer specimens, with another 11% of specimens exhibiting low-level gain spanning that locus. The 22q11.21 amplicon core contained eight named genes, only four of which were overexpressed (by transcript profiling) when amplified. Among these, CRKL encodes an adapter protein functioning in signal transduction, best known as a substrate of the BCR-ABL kinase in chronic myelogenous leukemia. RNA-interference-mediated knockdown of CRKL in lung cancer cell lines with (but not without) amplification led to significantly decreased cell proliferation, cell-cycle progression, cell survival, and cell motility and invasion. In addition, overexpression of CRKL in immortalized human bronchial epithelial cells led to enhanced growth factor-independent cell growth. Our findings indicate that amplification and resultant overexpression of CRKL contribute to diverse oncogenic phenotypes in lung cancer, with implications for targeted therapy, and highlight a role of adapter proteins as primary genetic drivers of tumorigenesis.

• Authors: Y H Kim, K A Kwei, L Girard, K Salari, J Kao, M Pacyna-Gengelbach, P Wang, T Hernandez-Boussard, A F Gazdar, I Petersen, J D Minna, J R Pollack
• Journal: Oncogene (Oncogene) Vol. 29 Issue 10 Pg. 1421-30 (Mar 11 2010) ISSN: 1476-5594 [Electronic] England
• PMID: 19966867 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)

Chemical References

• Adaptor Proteins, Signal Transducing
• CRKL protein
• Nuclear Proteins

Topics

• Adaptor Proteins, Signal Transducing (genetics, metabolism, physiology)
• Blotting, Western
• Carcinoma, Non-Small-Cell Lung (genetics, pathology, physiopathology)
• Cell Line, Tumor
• Cell Movement
• Cell Proliferation
• Cell Survival
• Chromosomes, Human, Pair 22 (genetics)
• Comparative Genomic Hybridization
• Gene Amplification
• Gene Expression Profiling
• Humans
• In Situ Hybridization, Fluorescence
• Lung Neoplasms (genetics, pathology, physiopathology)
• Nuclear Proteins (genetics, metabolism, physiology)
• Oligonucleotide Array Sequence Analysis
• RNA Interference