S
Shenda Gu
Researcher at Oregon Health & Science University
Publications - 22
Citations - 2348
Shenda Gu is an academic researcher from Oregon Health & Science University. The author has contributed to research in topics: Cancer & Small interfering RNA. The author has an hindex of 12, co-authored 18 publications receiving 1861 citations. Previous affiliations of Shenda Gu include Lawrence Berkeley National Laboratory.
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Journal ArticleDOI
Subtypes of pancreatic ductal adenocarcinoma and their differing responses to therapy.
Eric A. Collisson,Anguraj Sadanandam,Anguraj Sadanandam,Peter Olson,Peter Olson,William J. Gibb,William J. Gibb,Morgan L. Truitt,Shenda Gu,J. Cooc,Jennifer Weinkle,Grace E. Kim,Lakshmi Jakkula,Heidi S. Feiler,Andrew H. Ko,Adam B. Olshen,Kathleen L Danenberg,Margaret A. Tempero,Paul T. Spellman,Douglas Hanahan,Douglas Hanahan,Joe W. Gray,Joe W. Gray +22 more
TL;DR: Three PDA subtypes are defined: classical, quasimesenchymal and exocrine-like, and evidence for clinical outcome and therapeutic response differences between them is presented, and gene signatures for these subtypes that may have utility in stratifying patients for treatment are defined.
Journal ArticleDOI
A Central Role for RAF→MEK→ERK Signaling in the Genesis of Pancreatic Ductal Adenocarcinoma
Eric A. Collisson,Christy L. Trejo,Jillian M. Silva,Shenda Gu,James E. Korkola,Laura M. Heiser,Roch-Philippe Charles,Brian Rabinovich,Byron Hann,David Dankort,Paul T. Spellman,Wayne A. Phillips,Joe W. Gray,Martin McMahon +13 more
TL;DR: It is shown that expression of BRAF(V600E), but not PIK3CA(H1047R), in the mouse pancreas leads to pancreatic intraepithelial neoplasia (PanIN) lesions, and RAF→MEK→ERK signaling is central to the initiation and maintenance of PDA and to rational combination strategies in this disease.
Journal ArticleDOI
Nanoparticle-Mediated Systemic Delivery of siRNA for Treatment of Cancers and Viral Infections
Mohamed Shehata Draz,Binbin Amanda Fang,Pengfei Zhang,Zhi Hu,Shenda Gu,Kevin C. Weng,Joe W. Gray,Fanqing Frank Chen +7 more
TL;DR: This review summarizes the various nanoparticulate systems developed so far in the literature for systemic delivery of siRNA, which include silica and silicon-based nanoparticles, metal and metal oxides nanoparticle, carbon nanotubes, graphene, dendrimers, polymers, cyclodextrins, lipids, hydrogels, and semiconductor nanocrystals.
Journal ArticleDOI
Cationic Polymer Modified Mesoporous Silica Nanoparticles for Targeted siRNA Delivery to HER2+ Breast Cancer
Worapol Ngamcherdtrakul,Jingga Morry,Shenda Gu,David J. Castro,Shaun M. Goodyear,Thanapon Sangvanich,Moataz Reda,Richard Lee,Samuel A. Mihelic,Brandon L. Beckman,Zhi Hu,Joe W. Gray,Wassana Yantasee +12 more
TL;DR: Results suggest that this siHER2‐nanoparticle is ready for clinical evaluation and have an excellent safety profile in terms of blood compatibility and low cytokine induction, when exposed to human peripheral blood mononuclear cells.
Journal ArticleDOI
The expression level of HJURP has an independent prognostic impact and predicts the sensitivity to radiotherapy in breast cancer
Zhi Hu,Zhi Hu,Ge Huang,Anguraj Sadanandam,Shenda Gu,Marc E. Lenburg,Marc E. Lenburg,Melody Y. Pai,Nora Bayani,Eleanor A. Blakely,Joe W. Gray,Joe W. Gray,Jian-Hua Mao +12 more
TL;DR: HJURP mRNA level is a prognostic factor for disease-free and overall survival in patients with breast cancer and is a predictive biomarker for sensitivity to radiotherapy, according to a multivariate Cox proportional-hazard regression.