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Updated: Aug 1, 2025

Cell Cycle-specific Measurement of γH2AX and Apoptosis After Genotoxic Stress by Flow Cytometry
Published on: September 1, 2019
DDIAS, DNA damage-induced apoptosis suppressor, is a potential therapeutic target in cancer
Joo-Young Im1, Mi-Jung Kang2, Bo-Kyung Kim2,3,4
1Personalized Genomic Medicine Research Center, KRIBB, Daejeon, 34141, Republic of Korea. imjy@kribb.re.kr.
Abstract:
Increasing evidence indicates that DNA damage-induced apoptosis suppressor (DDIAS) is an oncogenic protein that is highly expressed in a variety of cancers, including colorectal cancer, lung cancer, breast cancer, and hepatocellular carcinoma (HCC). The discovery of DDIAS as a novel therapeutic target and its role in human cancer biology is fascinating and noteworthy. Recent studies have shown that DDIAS is involved in tumorigenesis, metastasis, DNA repair and synthesis, and drug resistance and that it plays multiple roles with distinct binding partners in several human cancers. This review focuses on the function of DDIAS and its regulatory proteins in human cancer as potential targets for cancer therapy, as well as the development and future prospects of DDIAS inhibitors.
Insights
DNA damage-induced apoptosis suppressor (DDIAS) is an oncogenic protein found in many cancers. Targeting DDIAS and its regulatory proteins offers a promising new avenue for cancer therapy development.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- DNA damage-induced apoptosis suppressor (DDIAS) is increasingly recognized as an oncogenic protein.
- High expression of DDIAS is observed in various cancers, including colorectal, lung, breast, and hepatocellular carcinoma (HCC).
Purpose of the Study:
- To review the multifaceted roles of DDIAS in human cancer biology.
- To explore DDIAS and its regulatory proteins as potential therapeutic targets.
- To discuss the development and future prospects of DDIAS inhibitors.
Main Methods:
- Literature review of recent studies on DDIAS function and regulation in cancer.
- Analysis of DDIAS involvement in tumorigenesis, metastasis, DNA repair, and drug resistance.
- Examination of DDIAS binding partners and their roles in different cancer types.
Main Results:
- DDIAS is implicated in key cancer processes such as tumor initiation, spread, DNA maintenance, and treatment resistance.
- DDIAS exhibits diverse functions mediated by various binding partners across different human cancers.
- The protein's oncogenic nature highlights its significance in cancer progression.
Conclusions:
- DDIAS represents a significant and novel therapeutic target for various human cancers.
- Understanding DDIAS regulatory proteins is crucial for developing effective cancer therapies.
- Further research into DDIAS inhibitors holds promise for future cancer treatment strategies.
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