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Emerging roles of dehydrogenase/reductase (DHRS) in cancer
Jun Huang1, Chenpeng Tang1, Xue Chen2
1Hunan Key Laboratory of Oncotarget Gene, Hunan Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan 410013, PR China; Key Laboratory of Carcinogenesis and Invasion, Chinese Ministry of Education, Cancer Research Institute, School of Basic Medicine, Central South University, Changsha, Hunan 410078, PR China.
Abstract:
As a member of short-chain dehydrogenase/reductase (SDR) superfamily, dehydrogenase/reductase (DHRS) is mainly involved in the metabolism of many substrates such as lipids, steroids and retinol. The DHRS family comprises more than 12 members, including DHRS1 - 4, DHRS6 - 13, among others. Several members have been extensively studied and implicated in tumorigenesis and cancer progression, such as DHRS2 involved in lipid metabolism, DHRS3/4/9/13 mediating all-trans retinoic acid biosynthesis, DHRS8/10/11 regulating steroid metabolism and DHRS6 maintaining intracellular iron homeostasis. Although the functions of other DHRS members remain poorly characterized, emerging evidence also suggests their association with cancer. Here, we provide an overview of the DHRS family members and highlight their roles in cancer progression.
Insights
The dehydrogenase/reductase (DHRS) family, part of the SDR superfamily, plays roles in metabolism and is increasingly linked to cancer progression. This review highlights known and emerging cancer-associated functions of DHRS members.
Area of Science:
- Biochemistry
- Molecular Biology
- Oncology
Background:
- The dehydrogenase/reductase (DHRS) family is a significant part of the short-chain dehydrogenase/reductase (SDR) superfamily.
- DHRS proteins are crucial for metabolizing lipids, steroids, and retinol.
- The DHRS family has over 12 members, with several implicated in cancer.
Purpose of the Study:
- To provide a comprehensive overview of the DHRS family.
- To highlight the known and emerging roles of DHRS members in cancer progression.
- To consolidate current knowledge on DHRS family functions in tumorigenesis.
Main Methods:
- Literature review
- Bioinformatic analysis (implied)
- Functional annotation of DHRS members
Main Results:
- Specific DHRS members (DHRS2, DHRS3/4/9/13, DHRS8/10/11, DHRS6) have characterized roles in lipid, retinoic acid, and steroid metabolism, and iron homeostasis, with links to cancer.
- Emerging evidence suggests broader associations between other DHRS family members and cancer.
- The diverse metabolic functions of DHRS proteins underscore their potential impact on cellular processes relevant to cancer.
Conclusions:
- The DHRS family represents a critical group of enzymes with diverse metabolic functions.
- Dysregulation of DHRS members is increasingly recognized as a factor in tumorigenesis and cancer progression.
- Further research into the less-characterized DHRS members may reveal novel therapeutic targets for cancer.
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