TY - JOUR
T1 - MiR-92b and miR-9/9* are specifically expressed in brain primary tumors and can be used to differentiate primary from metastatic brain tumors
AU - Nass, Dvora
AU - Rosenwald, Shai
AU - Meiri, Eti
AU - Gilad, Shlomit
AU - Tabibian-Keissar, Hilla
AU - Schlosberg, Anat
AU - Kuker, Hagit
AU - Sion-Vardy, Netta
AU - Tobar, Ana
AU - Kharenko, Oleg
AU - Sitbon, Einat
AU - Lithwick Yanai, Gila
AU - Elyakim, Eran
AU - Cholakh, Hila
AU - Gibori, Hadas
AU - Spector, Yael
AU - Bentwich, Zvi
AU - Barshack, Iris
AU - Rosenfeld, Nitzan
PY - 2009/7
Y1 - 2009/7
N2 - A recurring challenge for brain pathologists is to diagnose whether a brain malignancy is a primary tumor or a metastasis from some other tissue. The accurate diagnosis of brain malignancies is essential for selection of proper treatment. MicroRNAs are a class of small non-coding RNA species that regulate gene expression; many exhibit tissue-specific expression and are misregulated in cancer. Using microRNA expression profiling, we found that hsa-miR-92b and hsa-miR-9/hsa-miR-9* are over-expressed, specifically in brain primary tumors, as compared to primary tumors from other tissues and their metastases to the brain. By considering the expression of only these two microRNAs, it is possible to distinguish between primary and metastatic brain tumors with very high accuracy. These microRNAs thus represent excellent biomarkers for brain primary tumors. Previous reports have found that hsa-miR-92b and hsa-miR-9/hsa-miR-9* are expressed more strongly in developing neurons and brain than in adult brain. Thus, their specific over-expression in brain primary tumors supports a functional role for these microRNAs or a link between neuronal stem cells and brain tumorigenesis.
AB - A recurring challenge for brain pathologists is to diagnose whether a brain malignancy is a primary tumor or a metastasis from some other tissue. The accurate diagnosis of brain malignancies is essential for selection of proper treatment. MicroRNAs are a class of small non-coding RNA species that regulate gene expression; many exhibit tissue-specific expression and are misregulated in cancer. Using microRNA expression profiling, we found that hsa-miR-92b and hsa-miR-9/hsa-miR-9* are over-expressed, specifically in brain primary tumors, as compared to primary tumors from other tissues and their metastases to the brain. By considering the expression of only these two microRNAs, it is possible to distinguish between primary and metastatic brain tumors with very high accuracy. These microRNAs thus represent excellent biomarkers for brain primary tumors. Previous reports have found that hsa-miR-92b and hsa-miR-9/hsa-miR-9* are expressed more strongly in developing neurons and brain than in adult brain. Thus, their specific over-expression in brain primary tumors supports a functional role for these microRNAs or a link between neuronal stem cells and brain tumorigenesis.
KW - MicroRNA expression
KW - Molecular diagnostics
KW - Tumor classification
UR - http://www.scopus.com/inward/record.url?scp=66949150988&partnerID=8YFLogxK
U2 - 10.1111/j.1750-3639.2008.00184.x
DO - 10.1111/j.1750-3639.2008.00184.x
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AN - SCOPUS:66949150988
SN - 1015-6305
VL - 19
SP - 375
EP - 383
JO - Brain Pathology
JF - Brain Pathology
IS - 3
ER -