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Xue-Gong Fan

Researcher at Central South University

Publications -  41
Citations -  664

Xue-Gong Fan is an academic researcher from Central South University. The author has contributed to research in topics: HBsAg & Hepatitis B virus. The author has an hindex of 12, co-authored 41 publications receiving 432 citations.

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CircRNA-5692 inhibits the progression of hepatocellular carcinoma by sponging miR-328-5p to enhance DAB2IP expression.

TL;DR: The circRNA-5692–miR-328-5p–DAB2IP regulatory pathway inhibits the progression of HCC and may provide potential new targets for the diagnosis and therapy of H CC.
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A novel lncRNA, TCONS_00006195, represses hepatocellular carcinoma progression by inhibiting enzymatic activity of ENO1

TL;DR: Results suggest that lncRNA-6195 represses the growth of HCC by inhibiting the enzymatic activity of ENO1, and can serve as a basis for the development of novel strategies to hinder HCC.
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SPAG5 promotes proliferation and suppresses apoptosis in bladder urothelial carcinoma by upregulating Wnt3 via activating the AKT/mTOR pathway and predicts poorer survival.

TL;DR: Mechanistic investigations showed that SPAG5 promotes proliferation and suppresses apoptosis in BUC at least partially via upregulating Wnt3 through activating the AKT/mTOR signaling pathway, and the importance of the SPAg5/AKT-mTOR/Wnt3 axis identified in B UC cell models was confirmed.
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Radiation-promoted CDC6 protein stability contributes to radioresistance by regulating senescence and epithelial to mesenchymal transition.

TL;DR: Cell models for IR-induced senescence, apoptosis resistance, and EMT, three major mechanisms by which radioresistance develops are described, suggesting that CDC6highKI67low represents a new diagnostic marker of radiosensitivity, and CDC6 represents anew therapeutic target for cancer radiosensitization.
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Hepatitis B virus X protein inhibits apoptosis by modulating endoplasmic reticulum stress response

TL;DR: A novel mechanism of theHBx-mediated oncogenesis is revealed and provides a basis for potential HBx-targeted therapeutic intervention of HCC.