DDIAS, DNA damage-induced apoptosis suppressor, is a potential therapeutic target in cancer

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dc.contributor.authorJoo-Young Im-
dc.contributor.authorMi-Jung Kang-
dc.contributor.authorBo Kyung Kim-
dc.contributor.authorMi Sun Won-
dc.date.accessioned2023-06-05T16:33:22Z-
dc.date.available2023-06-05T16:33:22Z-
dc.date.issued2023-
dc.identifier.issn1226-3613-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/32055-
dc.description.abstractIncreasing 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.-
dc.publisherSpringer-Nature Pub Group-
dc.titleDDIAS, DNA damage-induced apoptosis suppressor, is a potential therapeutic target in cancer-
dc.title.alternativeDDIAS, DNA damage-induced apoptosis suppressor, is a potential therapeutic target in cancer-
dc.typeArticle-
dc.citation.titleExperimental and Molecular Medicine-
dc.citation.number5-
dc.citation.endPage885-
dc.citation.startPage879-
dc.citation.volume55-
dc.contributor.affiliatedAuthorJoo-Young Im-
dc.contributor.affiliatedAuthorMi-Jung Kang-
dc.contributor.affiliatedAuthorBo Kyung Kim-
dc.contributor.affiliatedAuthorMi Sun Won-
dc.contributor.alternativeName임주영-
dc.contributor.alternativeName강미정-
dc.contributor.alternativeName김보경-
dc.contributor.alternativeName원미선-
dc.identifier.bibliographicCitationExperimental and Molecular Medicine, vol. 55, no. 5, pp. 879-885-
dc.identifier.doi10.1038/s12276-023-00974-6-
dc.description.journalClassY-
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Division of A.I. & Biomedical Research > Genomic Medicine Research Center > 1. Journal Articles
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