Related Experiment Video
Updated: Jan 18, 2026

Author Spotlight: Unveiling Transmembrane Protein Family-Related Markers in Gastric Cancer and Implications for Targeted Therapies
Published on: September 15, 2023
ISG20: The multifaceted 'molecular star' in cancer research (Review)
Xinhui Zhu1, Shihao Jiang1, Lipeng Zhang1
1Department of Gastrointestinal Surgery, The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi 330006, P.R. China.
Abstract:
IFN‑stimulated gene (ISG)20 is a key member of the ISG family, serving a central role in antiviral defense, immune regulation and cell metabolism through its exonuclease activity. ISG20 is markedly dysregulated in various malignancies, including clear cell renal cell carcinoma, glioma, breast cancer and hepatocellular carcinoma, and it is associated with tumor proliferation, metastasis, angiogenesis and immune evasion. Its dual regulatory roles, such as promoting tumor progression via the MMP9/CCND1 signaling axis or enhancing antitumor immunity by activating the IFN‑β pathway, highlight its complex involvement in tumor biology. The present review aimed to summarize the discovery, structural characteristics and physiological functions of ISG20, and its multifaceted roles in tumor development. Moreover, the potential of ISG20 as a novel biomarker, immunoadjuvant and therapeutic target is discussed, offering theoretical insight and translational directions for precision oncology.
Insights
Interferon-stimulated gene (ISG)20, a key protein in immunity and metabolism, shows complex roles in cancer. This review explores ISG20
Area of Science:
- Immunology
- Molecular Biology
- Oncology
Background:
- Interferon-stimulated gene (ISG)20 is integral to antiviral defense, immune regulation, and cell metabolism via its exonuclease activity.
- ISG20 dysregulation is observed in clear cell renal cell carcinoma, glioma, breast cancer, and hepatocellular carcinoma, correlating with tumor progression and immune evasion.
Purpose of the Study:
- To review the discovery, structure, and functions of ISG20.
- To elucidate the multifaceted roles of ISG20 in tumor development and its dual regulatory functions in cancer biology.
- To discuss ISG20's potential as a biomarker, immunoadjuvant, and therapeutic target for precision oncology.
Main Methods:
- Literature review of ISG20's discovery, structure, and functions.
- Analysis of ISG20's involvement in various malignancies.
- Examination of ISG20's signaling pathways (e.g., MMP9/CCND1, IFN-β).
Main Results:
- ISG20 exhibits dual roles: promoting tumor progression via MMP9/CCND1 and enhancing antitumor immunity via IFN-β.
- Dysregulation of ISG20 is linked to tumor proliferation, metastasis, angiogenesis, and immune evasion in multiple cancers.
- ISG20's complex involvement in tumor biology is highlighted by its diverse regulatory functions.
Conclusions:
- ISG20 is a critical factor in cancer development with significant implications for tumor biology.
- ISG20 presents potential as a novel biomarker and therapeutic target in precision oncology.
- Further research into ISG20 could offer translational insights for cancer treatment and immunotherapy.
More Related Videos
Related Concept Videos
Adaptive Mechanisms in Cancer Cells
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
Cancer Stem Cells and Tumor Maintenance
Cancer stem cells are thought to originate from tissue-specific normal stem cells or progenitor cells. The normal stem cells usually reside in...
Targeted Cancer Therapies
There are several types of targeted therapies against...
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
Cancer Therapies
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...

