Feb 18 2010
Rosetta Genomics, Ltd. (NASDAQ: ROSG), a leading developer and provider 
      of microRNA-based molecular diagnostics, announced today that the 
      results of a joint study with the NYU Langone Medical Center were 
      published online on February 16th, 2010, and are set to be 
      published in the March 1st issue of the American Association 
      for Cancer Research’s journal, Cancer Research. The study, 
      “Hsa-Mir-29c* is Linked to the Prognosis of Malignant Pleural 
      Mesothelioma,” demonstrates the potential of a single microRNA to act as 
      an independent prognostic factor for time to progression as well as 
      survival after surgery. The abstract of the study may be viewed online 
      at: http://cancerres.aacrjournals.org/cgi/content/abstract/0008-5472.CAN-09-3993v1
    
“This is an exciting discovery which may have significant clinical 
      impact on the treatment of MPM”
    
      In the study, 142 MPM tumors were analyzed for microRNA expression 
      levels using Rosetta Genomics’ proprietary microRNA-based array and 
      qRT-PCR technologies. The results clearly demonstrate that higher levels 
      of miR-29c* in MPM predict a more favorable prognosis. Not only was the 
      microRNA able to separate MPM patients by time to progression after 
      surgery, but it also stratified these patients by their survival.
    
    
      When examining Time to Progression (TTP) of MPM, the expression level of 
      miR-29c* enabled the identification of two groups with significantly 
      different median TTP: 4 months versus 14 months in the study’s training 
      set, and 5.5 months versus 12.8 months in the study’s test set.
    
    
      When examining survival rates for MPM, the expression level of miR-29c* 
      enabled the identification of two groups as well: median survival of 8 
      months versus 32 months in the study’s training set, and median survival 
      of 9.1 months versus 21.6 months in the study’s test set. This new 
      diagnostic capability may help physicians apply more aggressive 
      therapeutic modalities to the poor prognosis group.
    
    
      Furthermore, the study found that over-expression of miR-29c* in 
      mesothelioma cell lines resulted in significantly decreased 
      proliferation, migration, invasion and colony formation.
    
    
      “This is an exciting discovery which may have significant clinical 
      impact on the treatment of MPM,” said Harvey Pass, M.D., Professor and 
      Chief, Division of Thoracic Surgery and Thoracic Oncology at NYU Langone 
      Medical Center, and the lead investigator of this study. “While MPM is 
      an aggressive cancer, our study showed that we can use a single microRNA 
      to identify subgroups of patients who differ significantly in their time 
      to progression and survival. When applied to a clinical setting, these 
      findings may enable clinicians to apply multimodality therapy to the 
      most appropriate patients. Furthermore, I think it is remarkable that a 
      single biomarker can provide such insights into disease prognosis.”
    
    
      “In addition to the significant clinical importance of being able to 
      forecast outcomes of MPM, this study demonstrates the tremendous 
      potential microRNAs hold as biomarkers,” noted Kenneth A. Berlin, 
      President and CEO of Rosetta Genomics. “NYU Langone Medical Center chose 
      Rosetta Genomics’ platform technology for this study as it was the most 
      technologically advanced, offering an extremely high sensitivity and 
      specificity suitable for studying microRNAs in the clinical setting. The 
      results of this study further validate the strength of our microRNA 
      platform technologies and our ability to leverage that strength to help 
      advance the standard of care.”