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1.
Experimental & Molecular Medicine ; : e272-2016.
Artículo en Inglés | WPRIM | ID: wpr-210167

RESUMEN

We found that non-small-cell lung cancer (NSCLC) cells express high levels of multiple aldehyde dehydrogenase (ALDH) isoforms via an informatics analysis of metabolic enzymes in NSCLC and immunohistochemical staining of NSCLC clinical tumor samples. Using a multiple reaction-monitoring mass spectrometry analysis, we found that multiple ALDH isozymes were generally abundant in NSCLC cells compared with their levels in normal IMR-90 human lung cells. As a result of the catalytic reaction mediated by ALDH, NADH is produced as a by-product from the conversion of aldehyde to carboxylic acid. We hypothesized that the NADH produced by ALDH may be a reliable energy source for ATP production in NSCLC. This study revealed that NADH production by ALDH contributes significantly to ATP production in NSCLC. Furthermore, gossypol, a pan-ALDH inhibitor, markedly reduced the level of ATP. Gossypol combined with phenformin synergistically reduced the ATP levels, which efficiently induced cell death following cell cycle arrest.


Asunto(s)
Humanos , Adenosina Trifosfato , Aldehído Deshidrogenasa , Puntos de Control del Ciclo Celular , Muerte Celular , Metabolismo Energético , Gosipol , Informática , Isoenzimas , Pulmón , Neoplasias Pulmonares , Espectrometría de Masas , NAD , Fenformina , Isoformas de Proteínas
2.
Genomics & Informatics ; : 159-162, 2009.
Artículo en Inglés | WPRIM | ID: wpr-10790

RESUMEN

Human personal genome sequencing can be done with high efficiency by aligning a huge number of short reads derived from various next generation sequencing (NGS) technologies to the reference genome sequence. One of the major obstacles is the incompleteness of human reference genome. We tried to analyze the effect of hidden gene duplication on the NGS data using the known example of hydin gene. Hydin2 , a duplicated copy of hydin on chromosome 16q22, has been recently found to be localized to chromosome 1q21, and is not included in the current version of standard human genome reference. We found that all of eight personal genome data published so far do not contain hydin2, and there is large number of nsSNPs in hydin. The heterozygosity of those nsSNPs was significantly higher than expected. The sequence coverage depth in hydin gene was about two fold of average depth. We believe that these unique finding of hydin can be used as useful indicators to discover new hidden multiplication in human genome.


Asunto(s)
Humanos , Proteína Coat de Complejo I , Duplicación de Gen , Genoma , Genoma Humano
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