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Jeewon Kim

Researcher at Stanford University

Publications -  23
Citations -  6789

Jeewon Kim is an academic researcher from Stanford University. The author has contributed to research in topics: Metastasis & Cancer. The author has an hindex of 14, co-authored 21 publications receiving 5970 citations. Previous affiliations of Jeewon Kim include University of California, Berkeley & Seoul National University.

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Boosting Cancer Immunotherapy with Anti-CD137 Antibody Therapy

TL;DR: The recent advances and clinical promise of agonistic anti-CD137 monoclonal antibody therapy are discussed and the potential to improve cancer treatment is discussed.
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Discovery of a novel class of covalent inhibitor for aldehyde dehydrogenases.

TL;DR: The discovery of a general class of ALDH inhibitors with a common mechanism of action is reported, and it is demonstrated that these inhibitors undergo an enzyme-mediated β-elimination reaction generating a vinyl ketone intermediate that covalently modifies the active site cysteine residue present in these enzymes.
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In vivo demonstration of enhanced radiotherapy using rare earth doped titania nanoparticles

TL;DR: It is shown here that intratumoural injection of RE doped titania nanoparticles can enhance the efficacy of radiotherapy in vivo, and can result in generation of ROS leading to cell death in a tumour-localized manner.
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Sustained inhibition of PKCα reduces intravasation and lung seeding during mammary tumor metastasis in an in vivo mouse model.

TL;DR: Data show that pharmacological inhibition ofPKCα effectively reduces mammary cancer metastasis by targeting intravasation and lung seeding steps in the metastatic process and suggest that PKCα-specific inhibitors, such as αV5-3, can be used to study the mechanistic roles of PKC α specifically and may provide a safe and effective treatment for the prevention of lung metastasis of breast cancer patients.
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Centrosomal PKCβII and Pericentrin Are Critical for Human Prostate Cancer Growth and Angiogenesis

TL;DR: It is found that the proliferation rates of endothelial and tumor cells oscillate asynchronously during the growth of human prostate cancer xenografts and that a PKCbetaII inhibitor may be used to reduce prostate cancer growth by targeting both angiogenesis and tumor cell growth.