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Heritable mutations of ALK main cause of familial neuroblastoma
Roches' xCELLigence cell analysis system useful in cancer research
Yaël Mossé and co-workers, from Philadelphia/PA, USA, studied twenty probands with neuroblastoma and a family history of the disease (1). A total of 176 individuals (49 affected with neuroblastoma) were genotyped genome-wide. The researchers identified a significant linkage signal at chromosome bands 2p23-24 using a whole-genome scan in neuroblastoma pedigrees. Resequencing of regional candidate genes showed three separate germline missense mutations in the tyrosine kinase domain of ALK that segregated with the disease in eight separate families. Resequencing in 194 high-risk neuroblastoma samples revealed somatically acquired mutations in the tyrosine kinase domain in 12.4% of samples. Nine of the ten mutations map to critical regions of the kinase domain and were predicted, with high probability, to be oncogenic drivers. Mutations resulted in constitutive phosphorylation, and targeted knockdown of ALK messenger RNA resulted in profound inhibition of growth in all cell lines harboring mutant or amplified ALK, as well as in two out of six wild-type cell lines for ALK. The effects of siRNA knockdown on substrate adherent growth were quantified using RT-CES System, the forerunner model of the new xCELLigence cell analysis system from Roche Applied Science.
The discovery of highly penetrant, heritable ALK mutations as the cause of hereditary neuroblastoma is of immediate relevance to probands with a family history, as the researchers concluded. Screening with non-invasive techniques such as sonography and measurement of urinary catecholamine metabolites should probably be implemented for unaffected children carrying an ALK mutation. In addition, the germline or acquired activation of the cell-surface kinase provides a tractable therapeutic target for this lethal pediatric malignancy.
Roche Applied Science's xCELLigence System - originally invented as Real-Time Cell Electronic Sensing System (RT-CES®) by the US-based ACEA Biosciences and co-developed by Roche and ACEA - allows label-free dynamic monitoring of cell proliferation and viability in real-time. The technique utilizes an electronic readout of impedance to non-invasively quantify cellular status in real-time. Cells are seeded in E-Plate microtiter plates, which are integrated with microelectronic sensor arrays. The interaction of cells with the microelectrode surface generates a cell-electrode impedance response, which not only indicates cell viability but also correlates with the number of the cells seeded in the well. For more information on the technology, please visit www.xcelligence.roche.com.
(1) Mossé Y et al.: Identification of ALK as a major familial neuroblastoma predisposition gene. Nature 2008 Aug 24, Epub ahead of print
(2) Maris, JM et al.: Chromosome 6p22 locus associated with clinically aggressive neuroblastoma. N Engl J Med 2008; 358: 2585-2593
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