GSGuanning Shang

Guanning Shang

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Guanning Shang has a total of 11 co-authors. Here are the top co-authors by number of shared publications:

  • Enduo Qiu

    Department of Bone and Soft Tissue Surgery, Cancer Hospital of China Medical University, Liaoning Cancer Hospital and Institute, Shenyang, Liaoning 110042, P.R. China

    1 shared publication
  • Jinxin Liu

    State Key Laboratory of Food Science and Technology School of Food Science and Technology Jiangnan University Wuxi China

    1 shared publication
  • Ke Zheng

    Department of Bone and Soft Tissue Tumor Surgery Cancer Hospital of China Medical University Liaoning Cancer Hospital & Institute Shenyang Liaoning Province China

    1 shared publication
  • Peter Wang

    Department of Medicine, Beijing Zhongwei Medical Research Center, China

    1 shared publication
  • Shizhe Li

    Department of Spine Surgery First Affiliated Hospital of Xinjiang Medical University Urumqi Xinjiang Uygur Autonomous Region China

    1 shared publication
  • Ting Chen

    Department of Orthopedics, Shengjing Hospital of China Medical University, Shenyang, Liaoning 110004, China

    1 shared publication

Latest Publications

  • The role of protein arginine N-methyltransferases in inflammation

    by Ting Chen, Jinxin Liu, Shizhe Li, Peter Wang, Guanning Shang


  • Retracted
    Open Access

    Ursolic acid suppresses the biological function of osteosarcoma cells

    by Yi Pei, Yueyan Zhang, Ke Zheng, Guanning Shang, Yuming Wang, Wei Wang, Enduo Qiu, Xiaojing Zhang

    Osteosarcoma is a highly malignant tumour that occurs in adolescents. Upregulation or the constitutive activation of epidermal growth factor receptor (EGFR) is a hallmark of osteosarcoma. To investigate the effect of ursolic acid on the biological function of osteosarcoma, MTT assay was used to detect the effect of ursolic acid on the proliferation of HOS and MG63 cells, while flow cytometry was used to analyse the effect on the cell cycle and apoptosis. Transwell and Matrigel assays were used to detect the effect of ursolic acid on cell migration and invasion, respectively. Western blot analysis and reverse transcription‑quantitative polymerase chain reaction were used to detect the effects of different concentrations of ursolic acid on EGFR signaling pathway‑related proteins, cell cycle, apoptosis and cell migration‑related proteins. After overexpression or silencing of EGFR, the effects of ursolic acid on EGFR pathway and cell biological function were subsequently detected, using the same methods. The present study identified that ursolic acid had inhibitory effects on the growth and metastatic ability of osteosarcoma cells by suppressing EGFR.