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Status |
Public on Jun 01, 2014 |
Title |
miR-28 expression in the Burkitt lymphoma cell line P3HR1 |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
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Summary |
Burkitt lymphoma (BL) is a highly aggressive B cell non-Hodgkin lymphoma (B-NHL), which originates from germinal center (GC) B cells and harbors translocations deregulating the MYC oncogene. A comparative analysis of microRNAs (miRNAs) expressed in normal and malignant GC B cells identified miR-28 as significantly down-regulated in BL, as well as in other GC-derived B-NHL. We show that re-expression of miR-28 impairs cell growth and clonogenic properties of BL cells by modulating several targets including MAD2L1, a component of the spindle checkpoint whose down-regulation is essential in mediating miR-28-induced growth-arrest, and BAG1, an activator of the ERK pathway.
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Overall design |
P3HR1 Burkitt lymphoma cell line was engineered to display inducible expression of GFP alone or GFP in combination with the miR-28 precursor from the pRTS1 vector upon doxycycline treatment. Two bulk populations (A and B) were established for both the control (GFP alone) and the miR28-expressing (GFP and miR-28 precursor) cells. Cells were induced with 0.1ug/ml doxycycline for 12h or 24h. Induction was performed on each bulk population in triplicates.
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Contributor(s) |
Schneider C, Basso K, Holmes AB, Dalla-Favera R |
Citation(s) |
24843176 |
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Submission date |
Mar 27, 2014 |
Last update date |
Mar 25, 2019 |
Contact name |
Riccardo Dalla-Favera |
E-mail(s) |
rd10@cumc.columbia.edu
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Organization name |
Columbia University
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Street address |
1130 St Nicholas Avenue
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City |
New York |
State/province |
NY |
ZIP/Postal code |
10032 |
Country |
USA |
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Platforms (1) |
GPL570 |
[HG-U133_Plus_2] Affymetrix Human Genome U133 Plus 2.0 Array |
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Samples (24)
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Relations |
BioProject |
PRJNA242802 |