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Xiubo Jiang

Researcher at Nanjing Tech University

Publications -  5
Citations -  211

Xiubo Jiang is an academic researcher from Nanjing Tech University. The author has contributed to research in topics: Apoptosis & Akt/PKB signaling pathway. The author has an hindex of 5, co-authored 5 publications receiving 116 citations.

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Oridonin exerts anticancer effect on osteosarcoma by activating PPAR-γ and inhibiting Nrf2 pathway

TL;DR: Oridonin exerted a dramatic pro-apoptotic effect by activating PPAR-γ and inhibiting Nrf2 pathway in vitro and in vivo, and may be a promising and effective agent for human osteosarcoma in the future clinical applications.
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Limonin ameliorates acetaminophen-induced hepatotoxicity by activating Nrf2 antioxidative pathway and inhibiting NF-κB inflammatory response via upregulating Sirt1.

TL;DR: Limonin mitigated APAP-induced hepatotoxicity by activating Nrf2 antioxidative pathway and inhibiting NF-κB inflammatory response via upregulating Sirt1, and demonstrated that limonin had therapeutic promise in AP AP-induced liver injury.
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Glaucocalyxin A reverses EMT and TGF-β1-induced EMT by inhibiting TGF-β1/Smad2/3 signaling pathway in osteosarcoma

TL;DR: It is demonstrated that Glaucocalyxin A inhibited EMT and TGF-β1-induced EMT by inhibiting TGF -β1/Smad2/3 signaling pathway in osteosarcoma.
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Glaucocalyxin A exerts anticancer effect on osteosarcoma by inhibiting GLI1 nuclear translocation via regulating PI3K/Akt pathway.

TL;DR: It is suggested that Glaucocalyxin A induced apoptosis in osteosarcoma by inhibiting nuclear translocation of GLI1 via regulating PI3K/Akt signaling pathway, which might be a potential candidate for human osteosARcoma in the future.
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Oridonin prevents epithelial-mesenchymal transition and TGF-β1-induced epithelial-mesenchymal transition by inhibiting TGF-β1/Smad2/3 in osteosarcoma.

TL;DR: Investigating the underlying mechanism of oridonin on EMT and metastasis of osteosarcoma found that oridon in inhibited migration and invasion of MG-63 and 143B cells and increased the protein expression of E-cadherin and decreased that of N- cadher in and Vimentin.