Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Bingchi Zeng has a total of 9 co-authors. Here are the top co-authors by number of shared publications:

  • Chuting Zhang

    School of Stomatology, Wenzhou Medical University, Wenzhou 325035, China

    1 shared publication
  • Deep K. Vaishnani

    School of International Studies, Wenzhou Medical University, Wenzhou 325035, Zhejiang Province, China

    1 shared publication
  • Hang Zhou

    Zhejiang Key Laboratory of Intelligent Cancer Biomarker Discovery and Translation, The First Affiliated Hospital of Wenzhou Medical University, School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou 325000, China

    1 shared publication
  • Huchao Mao

    The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China

    1 shared publication
  • Jianjian Zheng

    Zhejiang Key Laboratory of Intelligent Cancer Biomarker Discovery and Translation, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China

    1 shared publication
  • Jinglu Yu

    Zhejiang Key Laboratory of Intelligent Cancer Biomarker Discovery and Translation, The First Affiliated Hospital of Wenzhou Medical University, School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou 325000, China

    1 shared publication

Latest Publications

  • Open Access

    Multi-Omics and Experimental Validation Reveal Anti-HCC Mechanisms of Tibetan Liuwei Muxiang Pill and Quercetin

    by Wei Chen, Yanzhen Li, Chuting Zhang, Hang Zhou, Jun Ma, Deep K. Vaishnani, Bingchi Zeng, Jinglu Yu, Huchao Mao, Jianjian Zheng

    Background: Hepatocellular carcinoma (HCC) remains a significant therapeutic challenge due to its complex molecular mechanisms and limited effective treatments. Although the Tibetan medicine Liuwei Muxiang Pill (LWMX) has shown efficacy in gastric and colorectal cancer, no study has yet demonstrated its potential anti-HCC activity. Objective: To evaluate the therapeutic effects of LWMX on HCC. Methods: Integrating network pharmacology, high-resolution mass spectrometry, machine learning, and molecular dynamics simulations, combined with in vitro experiments for mechanism validation. Results: The study identified (Checkpoint kinase 1) CHK1 as a key target of LWMX in HCC regulation and confirmed that quercetin can form a stable complex with CHK1. In vitro experiments demonstrated that LWMX and its active component quercetin significantly inhibit the proliferation and migration of HCC cells. Conclusions: The study establishes CHK1 as a key therapeutic target, confirming the potential of LWMX and its core component quercetin in the treatment of HCC.