MicroRNA profiling reveals distinct signatures in B cell chronic lymphocytic leukemias

George A. Calin(National Cancer Institute), Chang‐Gong Liu(National Cancer Institute), Cinzia Sevignani(National Cancer Institute), Manuela Ferracin(National Cancer Institute), Nadia Felli(National Cancer Institute), Calin Dan Dumitru(National Cancer Institute), Masayoshi Shimizu(National Cancer Institute), Amelia Cimmino(National Cancer Institute), Simona Zupo(National Cancer Institute), Mariella Dono(National Cancer Institute), Marie L. Dell’Aquila(National Cancer Institute), Hansjüerg Alder(National Cancer Institute), Laura Z. Rassenti(National Cancer Institute), Thomas J. Kipps(National Cancer Institute), Florencia Bullrich(National Cancer Institute), Massimo Negrini(National Cancer Institute), Carlo M. Croce(National Cancer Institute)
Proceedings of the National Academy of Sciences
July 29, 2004
Cited by 1,294Open Access
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Abstract

Little is known about the expression levels or function of micro-RNAs (miRNAs) in normal and neoplastic cells, although it is becoming clear that miRNAs play important roles in the regulation of gene expression during development [Ambros, V. (2003) Cell 113, 673-676; McManus, M. T. (2003) Semin. Cancer Biol. 13, 253-258]. We now report the genomewide expression profiling of miRNAs in human B cell chronic lymphocytic leukemia (CLL) by using a microarray containing hundreds of human precursor and mature miRNA oligonucleotide probes. This approach allowed us to identify significant differences in miRNome expression between CLL samples and normal CD5+ B cells; data were confirmed by Northern blot analyses and real-time RT-PCR. At least two distinct clusters of CLL samples can be identified that were associated with the presence or absence of Zap-70 expression, a predictor of early disease progression. Two miRNA signatures were associated with the presence or absence of mutations in the expressed Ig variableregion genes or with deletions at 13q14, respectively. These data suggest that miRNA expression patterns have relevance to the biological and clinical behavior of this leukemia.


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