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Yan Shen
shenyan@nju.edu.cn
Chinese, English, Japanese
Jiangsu
Nanjing University
Life Sciences
  • 1992.09–1997.07 Bachelor: Shenyang Pharmaceutical University
  • 1997.09–2000.06 Master: Shenyang Pharmaceutical University
  • 2000.10–2005.05 Doctorate: Yokohama City University, Japan
  • Received the First Prize of the Natural Science Award for Outstanding Scientific Research Achievements in Higher Education Institutions twice
  • 2005.09–2007.12 Nanjing University, School of Life Sciences - Lecturer
  • 2007.12–Present Nanjing University, School of Life Sciences - Associate Professor
  • 2011.11–2012.11 Kyoto University, Japan - Visiting Scholar
  • 2019.11–2020.12 University of Pennsylvania, Perelman School of Medicine, USA - Visiting Scholar
  • 2010: Nanjing University Young Backbone Teacher
  • 2011: Jiangsu Province Teaching Achievement Award Second Prize
  • 2012: First Prize of the Natural Science Award for Outstanding Scientific Research Achievements in Higher Education Institutions (9/11)
  • 2015: Nanjing University Bank of China Young Teacher Achievement First Prize
  • 2019: First Prize of the Natural Science Award for Outstanding Scientific Research Achievements in Higher Education Institutions (7/8)
  • 2020: National First-Class Undergraduate Course
Research on tumor malignant progression and drug resistance mechanisms
Identification and mechanism of action of small molecule compounds with anti-tumor activity
Research on the pathogenesis of immune diseases and development of therapeutic drugs
  • Therapeutic effect of CpG-enriched plasmid administration on the tight-skin mouse model of scleroderma., Yan Shen, Motohide Ichino, Masatoshi Nakazawa, Takashi Ikejima, Yoshitsugu Kojima, Kenji Okuda, and Mutsuhiko Minami, 2005
  • CpG oligodeoxynucleotides prevent the development of scleroderma-like syndrome in tight-skin mice by stimulating a Th1 immune response., Yan Shen, Motohide Ichino, Masatoshi Nakazawa, and Mutsuhiko Minami, 2005
  • PRL-3 promotes the malignant progression of melanoma via triggering dephosphorylation and cytoplasmic localization of NHERF1., Fang XY, Song R, Chen W, Yang YY, Gu YH, Shu YQ, Wu XD, Wu XF, Sun Y*, Shen Y*, Xu Q*, 2015
  • Blockade of the interaction between Bcr-Abl and PTB1B by small molecule SBF-1 to overcome imatinib-resistance of chronic myeloid leukemia cells., Elgehama, A. Chen W, Pang J, Mi S, Li J, Guo W, Wang X, Gao J, Yu B, Shen Y*, Xu Q*, 2016
  • Small molecule RL71-triggered excessive autophagic cell death as a potential therapeutic strategy in triple-negative breast cancer., Gao J, Fan M, Peng S, Zhang M, Xiang G, Li X, Guo W, Sun Y, Wu X, Wu X, Liang G, Shen Y*, Xu Q*, 2017
  • Exosomal transfer of cisplatin-induced miR-425-3p confers cisplatin resistance in NSCLC through activating autophagy., Ma Y, Yuwen D, Chen JW, Zheng BF, Gao J, Fan M, Xue WW, Wang YX, Li WH, Shu Y, Xu Q*, Shen Y*, 2019
  • Triggering a switch from basal- to luminal-like breast cancer subtype by the small-molecule diptoindonesin G via induction of GABARAPL1., Fan M, Chen JW, Gao J, Xue WW, Wang YX, Li WH, Zhou L, Li X, Jiang CF, Sun Y, Wu XF, Wu XD, Ge H, Shen Y*, Xu Q*, 2020
  • Intracellular CYTL1, a novel tumor suppressor, stabilizes NDUFV1 to inhibit metabolic reprogramming in breast cancer., Xue WW, Li X, Li WH, Wang YX, Jiang CF, Zhou L, Gao J, Yu Y, Shen Y*, Xu Q*, 2022
  • Highly expressed SERCA2 triggers tumor cell autophagy and is a druggable vulnerability in triple-negative breast cancer., Fan M, Gao J, Zhou L, Xue WW, Wang YX, Chen JW, Li WH, Yu Y, Liu B, Shen Y*, Xu Q*, 2022
  • A plant-derived glucocorticoid receptor modulator with potency to attenuate the side effects of glucocorticoid therapy., Wang YX, Gao J, Yu Y, Zhou L, Miao W, Xue WW, Liu B, Wu XD, Wu XF, Gao HY*, Shen Y*, Xu Q*, 2023
Tumor Malignant Progression Drug Resistance Mechanisms Small Molecules Anti-Tumor Immune Diseases Therapeutic Drugs Pathogenesis

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