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DOI 10.1371/journal.pone.0082411

Медицинская библиотека · PloS one · 2013

The combined expression patterns of Ikaros isoforms characterize different hematological tumor subtypes.

Orozco Carlos A, Acevedo Andrés, Cortina Lazaro, Cuellar Gina E, Duarte Mónica, Martín Liliana, Mesa Néstor M, Muñoz Javier, Portilla Carlos A, Quijano Sandra M, Quintero Guillermo, Rodriguez Miriam, Saavedra Carlos E, Groot Helena, Torres María M, López-Segura Valeriano

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

A variety of genetic alterations are considered hallmarks of cancer development and progression. The Ikaros gene family, encoding for key transcription factors in hematopoietic development, provides several examples as genetic defects in these genes are associated with the development of different types of leukemia. However, the complex patterns of expression of isoforms in Ikaros family genes has prevented their use as clinical markers. In this study, we propose the use of the expression profiles of the Ikaros isoforms to classify various hematological tumor diseases. We have standardized a quantitative PCR protocol to estimate the expression levels of the Ikaros gene exons. Our analysis reveals that these levels are associated with specific types of leukemia and we have found differences in the levels of expression relative to five interexonic Ikaros regions for all diseases studied. In conclusion, our method has allowed us to precisely discriminate between B-ALL, CLL and MM cases. Differences between the groups of lymphoid and myeloid pathologies were also identified in the same way.

Для цитирования: Orozco Carlos A, Acevedo Andrés, Cortina Lazaro, Cuellar Gina E, Duarte Mónica, Martín Liliana, Mesa Néstor M, Muñoz Javier, Portilla Carlos A, Quijano Sandra M, Quintero Guillermo, Rodriguez Miriam, Saavedra Carlos E, Groot Helena, Torres María M, López-Segura Valeriano. The combined expression patterns of Ikaros isoforms characterize different hematological tumor subtypes.. PloS one. 2013. DOI: 10.1371/journal.pone.0082411.

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