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Identifying Inhibitors of the HBx-DDB1 Interaction Using a Split Luciferase Assay System
Published on: December 21, 2019
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Research progress on oncoprotein hepatitis B X‑interacting protein (Review).
Lei Cheng1, Lijuan Guo2, Teng Zou2
1Chronic Disease Research Center, Medical College, Dalian University, Dalian, Liaoning 116622, P.R. China.
Molecular Medicine Reports
|April 5, 2024
Summary
Hepatitis B X-interacting protein (HBXIP) promotes tumor progression by enhancing antioxidant capacity and inhibiting ferroptosis. This review details HBXIP
Area of Science:
- Oncology
- Molecular Biology
Background:
- Hepatitis B X-interacting protein (HBXIP), encoded by the Lamtor gene, is a lysosomal membrane protein.
- HBXIP is overexpressed in various cancers, including breast, esophageal, and liver cancers, correlating with specific clinicopathological features.
Approach:
- This review synthesizes current research on HBXIP's multifaceted roles in tumorigenesis.
- It examines HBXIP's normal physiological functions, oncogenic mechanisms, and clinical significance.
Key Points:
- HBXIP enhances tumor cell antioxidant capacity and inhibits ferroptosis.
- It regulates transcriptional, post-transcriptional, and post-translational processes in tumors.
- HBXIP drives metabolic reprogramming and malignant progression in cancer cells.
Conclusions:
- HBXIP is a key driver of tumor progression through diverse molecular mechanisms.
- Further research into HBXIP's carcinogenic pathways is warranted for therapeutic targeting.
Keywords:
ferroptosishepatitis B X‑interacting proteinoxidative stresspost‑transcriptionreviewtranscriptiontranslation
