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Status |
Public on Mar 04, 2022 |
Title |
A hotspot mutation targeting the R-RAS2 GTPase acts as a potent oncogenic driver in a wide spectrum of tumors |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
A missense change in RRAS2 (Gln72-to-Leu), analogous to the Gln61-to-Leu mutation of RAS oncoproteins, has been identified as a hotspot mutation in cancer and Noonan syndrome. However, the relevance of this mutation for in vivo tumorigenesis remains unknown. Here, we show that R-RAS2(Q72L) is required for optimal tumorigenic activity of human cancer cells.
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Overall design |
Genome-wide gene expression analyses of control and Rras2(Q72L) knockdown (sh#89) fibrosarcoma cells.
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Contributor(s) |
Fernández-Pisonero I, Clavaín L, Robles-Valero J, Lorenzo-Martín LF, Caloto R, Nieto B, García-Macías C, Oeste CL, Sánchez-Martín M, Abad A, Hortal A, Caballero D, González M, Vicente-Manzanares M, Dosil M, Alarcón B, Bustelo XR |
Citation(s) |
35294890 |
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Submission date |
Jul 04, 2021 |
Last update date |
Jun 03, 2022 |
Contact name |
L. Francisco Lorenzo-Martín |
E-mail(s) |
luis.lorenzomartin@epfl.ch
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Organization name |
École Polytechnique Fédérale de Lausanne (EPFL)
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Lab |
Laboratory of Stem Cell Bioengineering
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Street address |
EPFL – SV – IBI – LSCB – Station 15
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City |
Lausanne |
State/province |
Vaud |
ZIP/Postal code |
1015 |
Country |
Switzerland |
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Platforms (1) |
GPL23038 |
[Clariom_S_Mouse] Affymetrix Clariom S Assay, Mouse (Includes Pico Assay) |
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Samples (6)
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Relations |
BioProject |
PRJNA743644 |