D
Davide Ruggero
Researcher at University of California, San Francisco
Publications - 118
Citations - 20361
Davide Ruggero is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Translation (biology) & EIF4E. The author has an hindex of 49, co-authored 111 publications receiving 17167 citations. Previous affiliations of Davide Ruggero include Fox Chase Cancer Center & University of Bologna.
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Journal ArticleDOI
A single H/ACA small nucleolar RNA mediates tumor suppression downstream of oncogenic RAS.
Mary McMahon,Adrian Contreras,Mikael Holm,Tamayo Uechi,Craig M. Forester,Xiaming Pang,Cody Jackson,Meredith E. K. Calvert,Bin Chen,David A. Quigley,John M. Luk,R. Kate Kelley,John D. Gordan,Ryan M. Gill,Scott C. Blanchard,Davide Ruggero +15 more
TL;DR: A novel function for one H/ACA snoRNA, SNORA24, which guides two pseudouridine modifications within the small ribosomal subunit, in RAS-induced senescence in vivo is described and found that in mouse models, loss of Snora24 cooperates with RASG12V to promote the development of liver cancer that closely resembles human steatohepatitic hepatocellular carcinoma.
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Oncogenic AKTivation of translation as a therapeutic target.
TL;DR: It will be important to determine whether combined inhibition of ribosome biogenesis, translation initiation, and translation elongation can demonstrate improved therapeutic efficacy in tumours driven by oncogenic AKT.
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Leukemia with distinct phenotypes in transgenic mice expressing PML/RAR alpha, PLZF/RAR alpha or NPM/RAR alpha.
Eduardo Magalhães Rego,Davide Ruggero,Carla Tribioli,Giorgio Cattoretti,Scott C. Kogan,Robert L. Redner,Pier Paolo Pandolfi +6 more
TL;DR: The results underscore the critical relevance of the X moiety in dictating the biology of the disease and the activity of the APL fusion oncoprotein.
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The puzzling multiple lives of PML and its role in the genesis of cancer.
TL;DR: Despite the recent flurry of reports attributing multiple biological roles to the PML protein, PML still lacks a definitive biochemical function.
Journal ArticleDOI
The 4E-BP-eIF4E axis promotes rapamycin-sensitive growth and proliferation in lymphocytes.
Lomon So,Jongdae Lee,Jongdae Lee,Miguel Palafox,Sharmila Mallya,Chaz G. Woxland,Meztli Arguello,Morgan L. Truitt,Nahum Sonenberg,Davide Ruggero,David A. Fruman +10 more
TL;DR: The findings suggest that the 4E-BP–eIF4E axis is uniquely rapamycin-sensitive in lymphocytes and that this axis promotes clonal expansion of these cells by coordinating growth and proliferation.