J
Jun Fang
Researcher at Huazhong University of Science and Technology
Publications - 28
Citations - 335
Jun Fang is an academic researcher from Huazhong University of Science and Technology. The author has contributed to research in topics: Hematopoietic stem cell transplantation & Transplantation. The author has an hindex of 10, co-authored 27 publications receiving 267 citations.
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Mangiferin activates Nrf2-antioxidant response element signaling without reducing the sensitivity to etoposide of human myeloid leukemia cells in vitro.
TL;DR: Mangiferin is a novel Nrf2 activator that reduces oxidative stress and protects normal cells without reducing the sensitivity to etoposide of HL-60 leukemia cells in vitro and may be a potential chemotherapy adjuvant.
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Mangiferin increases Nrf2 protein stability by inhibiting its ubiquitination and degradation in human HL60 myeloid leukemia cells.
TL;DR: Evidence is provided that MA increases Nrf2 protein stability by inhibiting its ubiquitination and degradation in hematopoietic cells, which may be one of the mechanisms through which MA activates the NRF2-mediated antioxidant response and exerts cytoprotective effects.
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Endothelial microparticles delivering microRNA-155 into T lymphocytes are involved in the initiation of acute graft-versus-host disease following allogeneic hematopoietic stem cell transplantation.
Ran Zhang,Xiaoxiao Wang,Mei Hong,Ting Luo,Miaomiao Zhao,Haorui Shen,Jun Fang,Xiaojie Li,Sibin Zang,Ping Chen,Di-min Nie,Peng Zheng,Qiuling Wu,Linghui Xia +13 more
TL;DR: Analysis of EMPs found that EMPs derived from TNF-α-stimulated human umbilical vein endothelial cells concentrated more microRNA-155 (miR-155) compared with maternal cells, which provides a mechanistic framework in which miR- 155 delivered by EMPs is involved in aGVHD pathogenesis by activating specific T lymphocytes functions.
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Tissue factor/FVIIa activates Bcl-2 and prevents doxorubicin-induced apoptosis in neuroblastoma cells
TL;DR: In neuroblastoma cell lines overexpressed TF ligated with FVIIa produced upregulation of Bcl-2 expression through the JAK/STAT5 signaling pathway, resulting in resistance to apoptosis, surmise that this TF-FVIIa pathway may contribute, at least in part, to chemotherapy resistance in Neuroblastoma.
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Idarubicin-intensified haploidentical HSCT with GvHD prophylaxis of ATG and basiliximab provides comparable results to sibling donors in high-risk acute leukemia.
Ran Zhang,Wei Shi,Huafang Wang,Yong You,Zhaodong Zhong,Weiming Li,Chi Zhang,Xuan Lu,Wang Yd,Peng Zheng,Jun Fang,Mei Hong,Qiuling Wu,Linghui Xia +13 more
TL;DR: Data provide reinforcing evidence that the novel haplo-HSCT system could dramatically improve the survival of high-risk acute leukemia with low relapse and acceptable transplantation-related mortality, and might be a promising therapeutic option for high- risk patients.