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Jie Wu

Researcher at Soochow University (Suzhou)

Publications -  6
Citations -  340

Jie Wu is an academic researcher from Soochow University (Suzhou). The author has contributed to research in topics: Stem cell & Haematopoiesis. The author has an hindex of 3, co-authored 4 publications receiving 284 citations.

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Anti-leukemia activity of PVP-coated silver nanoparticles via generation of reactive oxygen species and release of silver ions

TL;DR: It is found that AgNPs could inhibit the viability of AML cells including the isolates from AML patients, and supported the model that both generation of ROS and release of silver ions played critical roles in the AgnPs-induced cytotoxic effect against AMl cells.
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Activation of autophagy by elevated reactive oxygen species rather than released silver ions promotes cytotoxicity of polyvinylpyrrolidone-coated silver nanoparticles in hematopoietic cells

TL;DR: It is suggested that autophagy is involved in the cytotoxicity of PVP-coated AgNPs in normal hematopoietic cells, and the inhibition of autophagic flux is a novel and potent strategy to protect normal heMatopoetic cells upon treatment with AgNNP.
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Growth arrest specific 2 is up-regulated in chronic myeloid leukemia cells and required for their growth.

TL;DR: GAS2 was up-regulated in CML cells including CD34+ progenitor cells compared to their normal counterparts and the inhibition of GAS2 impairs the growth of Cml cells, which indicates GAS1 is a novel regulator of C ML cells and a potential therapeutic target of this disease.
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ZFX modulates the growth of human leukemic cells via B4GALT1.

TL;DR: It is demonstrated that ZFX is aberrantly expressed in multiple human leukemic cells and it modulates the growth and drug response of leukeMIC cells partially via B4GALT1, which suggests that Z FX is a new regulator of leukedmic cells.
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Enhancing Natural Killer Cell-Mediated Cancer Immunotherapy by the Biological Macromolecule Nocardia rubra Cell-Wall Skeleton

TL;DR: The findings indicate that Nr-CWS could suppress the lung metastasis induced by B16F10 melanoma cells, which may be exerted through its effect on NK cells by promoting NK cell terminal differentiation (CD27lowCD11bhigh), and up-regulating the production of cytokines and cytotoxic molecules.