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Y. Jeffrey Wu

Researcher at Oregon Health & Science University

Publications -  11
Citations -  598

Y. Jeffrey Wu is an academic researcher from Oregon Health & Science University. The author has contributed to research in topics: Cisplatin & Ototoxicity. The author has an hindex of 8, co-authored 11 publications receiving 559 citations.

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Protection against Cisplatin-Induced Toxicities by N-Acetylcysteine and Sodium Thiosulfate as Assessed at the Molecular, Cellular, and in Vivo Levels

TL;DR: The chemoprotection route and timing of administration can be manipulated to maintain CDDP antitumor efficacy while protecting against toxicities.
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The Chemoprotective Agent N-Acetylcysteine Blocks Cisplatin-Induced Apoptosis through Caspase Signaling Pathway

TL;DR: Results show that NAC blocks both the death receptor and the mitochondrial apoptotic pathways induced by cisplatin, and provides an opportunity to manipulate route and timing to maintain cisPlatin antitumor efficacy while protecting against chemotherapy side effects.
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In vivo leukocyte labeling with intravenous ferumoxides/protamine sulfate complex and in vitro characterization for cellular magnetic resonance imaging

TL;DR: In vivo ferumoxides/protamine sulfate-loaded leukocytes and splenocytes were detected by MRI after intracerebral injection and might provide useful information for monitoring leukocyte trafficking into the brain.
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Targeting αv-integrins decreased metastasis and increased survival in a nude rat breast cancer brain metastasis model

TL;DR: Intetumumab treatment either in vitro prior to cell infusion or intravenous before or after cell infusion prevented metastasis formation on MRI and decreased the number of metastases on histology, suggesting that breast cancer patients at risk of metastase might benefit from early intetumuab treatment.
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N-acetylcysteine chemoprotection without decreased cisplatin antitumor efficacy in pediatric tumor models.

TL;DR: Data support a Phase I/II clinical trial of delayed NAC to reduce ototoxicity in children with localized pediatric cancers and support a minimally nephrotoxic cisplatin therapy if delayed until 4 h after chemotherapy.