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Oshrat Attar-Schneider

Meir Medical Center
Tel Aviv University

19

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230

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BM-MSCs-derived ECM modifies multiple myeloma phenotype and drug response in a source-dependent manner

2019 Translational Research
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Niche origin of mesenchymal stem cells derived microvesicles determines opposing effects on NSCLC: primary versus metastatic

2019 Cellular Signalling
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Multiple myeloma BM-MSCs increase the tumorigenicity of MM cells via transfer of VLA4 enriched microvesicles

2019 Carcinogenesis
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9P Mesenchymal stem cells' microvesicles from primary and metastatic NSCLC niches differentially modulate lung cancer cells

2018 Journal of Thoracic Oncology
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The effect of mesenchymal stem cells’ secretome on lung cancer progression is contingent on their origin: primary or metastatic niche

2018 Laboratory Investigation
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P3.01-034 Migration and Epithelial to Mesenchymal Transition of Lung Cancer Can Be Targeted via Translation Initiation Factors eIF4E and eIF4GI: Topic: Functional Biology in Lung Cancer

2017 Journal of Thoracic Oncology
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Letter to the Editor: miR‐199b‐3p and miR‐199a‐3p are isoforms with identical sequence and established function as tumor and metastasis suppressors

2017 Journal of Leukocyte Biology
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Microvesicles derived from normal and multiple myeloma bone marrow mesenchymal stem cells differentially modulate myeloma cells’ phenotype and translation initiation

2017 Carcinogenesis
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Mesenchymal stem cells secretomes' affect multiple myeloma translation initiation

2016 Cellular Signalling
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Multiple myeloma cells reprogram bone marrow mesenchymal stem cells’ translation initiation thereby promoting their migration

2016 European Journal of Cancer
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