• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

醛酮还原酶家族一个新成员在人体组织中的序列及表达水平

Sequence and expression levels in human tissues of a new member of the aldo-keto reductase family.

作者信息

Hyndman D J, Flynn T G

机构信息

Department of Biochemistry, Queen's University, Kingston, Canada.

出版信息

Biochim Biophys Acta. 1998 Aug 20;1399(2-3):198-202. doi: 10.1016/s0167-4781(98)00109-2.

DOI:10.1016/s0167-4781(98)00109-2
PMID:9765596
Abstract

We have isolated a human cDNA clone from small intestine that represents a new member of the aldo-keto reductase family. This new member showed 70% identity at the protein level to human aldose reductase and around 80% identity to other Chinese hamster and mouse reductases. The expression pattern shows that this message is located primarily in the adrenal gland, thus suggesting an involvement in steroid metabolism. It is also strongly expressed in the intestinal tract and has been called human small intestine reductase.

摘要

我们从小肠中分离出一个人类cDNA克隆,它代表醛糖-酮糖还原酶家族的一个新成员。这个新成员在蛋白质水平上与人类醛糖还原酶有70%的同源性,与其他中国仓鼠和小鼠的还原酶有大约80%的同源性。表达模式表明,这条信息主要位于肾上腺,因此提示其参与类固醇代谢。它在肠道中也有强烈表达,被称为人类小肠还原酶。

相似文献

1
Sequence and expression levels in human tissues of a new member of the aldo-keto reductase family.醛酮还原酶家族一个新成员在人体组织中的序列及表达水平
Biochim Biophys Acta. 1998 Aug 20;1399(2-3):198-202. doi: 10.1016/s0167-4781(98)00109-2.
2
A vertebrate aldo-keto reductase active with retinoids and ethanol.一种对类视黄醇和乙醇有活性的脊椎动物醛酮还原酶。
J Biol Chem. 2001 Jun 1;276(22):19132-40. doi: 10.1074/jbc.M010478200. Epub 2001 Feb 7.
3
Molecular cloning, expression and catalytic activity of a human AKR7 member of the aldo-keto reductase superfamily: evidence that the major 2-carboxybenzaldehyde reductase from human liver is a homologue of rat aflatoxin B1-aldehyde reductase.醛酮还原酶超家族人类AKR7成员的分子克隆、表达及催化活性:来自人肝脏的主要2-羧基苯甲醛还原酶是大鼠黄曲霉毒素B1-醛还原酶同系物的证据
Biochem J. 1998 May 15;332 ( Pt 1)(Pt 1):21-34. doi: 10.1042/bj3320021.
4
Human testis specific protein: a new member of aldo-keto reductase superfamily.人类睾丸特异性蛋白:醛糖酮还原酶超家族的新成员。
Chem Biol Interact. 2003 Feb 1;143-144:299-305. doi: 10.1016/s0009-2797(02)00187-4.
5
Structure and tissue-specific expression of the aldo-keto reductase superfamily.醛糖酮还原酶超家族的结构与组织特异性表达
Biochemistry. 1994 Mar 22;33(11):3223-8. doi: 10.1021/bi00177a012.
6
Cloning and expression of the cDNA encoding rabbit liver carbonyl reductase.编码兔肝脏羰基还原酶的cDNA的克隆与表达
Gene. 1995 Mar 10;154(2):297-8. doi: 10.1016/0378-1119(94)00843-h.
7
Characterization of a novel murine aldo-keto reductase.一种新型小鼠醛酮还原酶的特性分析。
Adv Exp Med Biol. 1997;414:455-64. doi: 10.1007/978-1-4615-5871-2_52.
8
Cloning, sequencing, and enzymatic activity of an inducible aldo-keto reductase from Chinese hamster ovary cells.中国仓鼠卵巢细胞中一种诱导型醛酮还原酶的克隆、测序及酶活性分析
J Biol Chem. 1997 May 16;272(20):13286-91. doi: 10.1074/jbc.272.20.13286.
9
All in the family: aldose reductase and closely related aldo-keto reductases.家族成员:醛糖还原酶及密切相关的醛酮还原酶
Cell Mol Life Sci. 2004 Apr;61(7-8):737-49. doi: 10.1007/s00018-003-3402-3.
10
Characterisation of genes encoding two novel members of the aldo-keto reductase superfamily.醛酮还原酶超家族两个新成员编码基因的特征分析
Biochem Int. 1992 Dec;28(4):651-7.

引用本文的文献

1
The pan-cancer landscape of aldo-keto reductase1B10 reveals that its expression is diminished in gastric cancer.醛酮还原酶1B10的泛癌图谱显示,其在胃癌中的表达降低。
Front Immunol. 2024 Dec 6;15:1488042. doi: 10.3389/fimmu.2024.1488042. eCollection 2024.
2
Differential Gene Expression Profiles Involved in the Inflammations Due to COVID-19 and Inflammatory Bowel Diseases and  the Investigation of Predictive Biomarkers.新型冠状病毒肺炎和炎症性肠病相关炎症中的差异基因表达谱及预测性生物标志物研究
Biochem Genet. 2024 Feb;62(1):311-332. doi: 10.1007/s10528-023-10414-9. Epub 2023 Jun 19.
3
Overexpression of AKR1B10 Predicts Poor Prognosis in Gastric Cancer Patients Undergoing Surgical Resection.
AKR1B10 过表达预示接受手术切除的胃癌患者预后不良。
Curr Oncol. 2022 Dec 21;30(1):85-99. doi: 10.3390/curroncol30010007.
4
The Role of AKR1B10 in Physiology and Pathophysiology.醛糖还原酶1B10(AKR1B10)在生理和病理生理中的作用
Metabolites. 2021 May 21;11(6):332. doi: 10.3390/metabo11060332.
5
Loss of AKR1B10 promotes colorectal cancer cells proliferation and migration via regulating FGF1-dependent pathway.AKR1B10 的缺失通过调节 FGF1 依赖性通路促进结直肠癌细胞的增殖和迁移。
Aging (Albany NY). 2020 Jul 2;12(13):13059-13075. doi: 10.18632/aging.103393.
6
Compensatory upregulation of aldo-keto reductase 1B10 to protect hepatocytes against oxidative stress during hepatocarcinogenesis.醛糖酮还原酶1B10的代偿性上调在肝癌发生过程中保护肝细胞免受氧化应激。
Am J Cancer Res. 2019 Dec 1;9(12):2730-2748. eCollection 2019.
7
Bioinformatic profiling identifies a platinum-resistant-related risk signature for ovarian cancer.生物信息学分析确定了一种卵巢癌铂耐药相关风险特征。
Cancer Med. 2020 Feb;9(3):1242-1253. doi: 10.1002/cam4.2692. Epub 2019 Dec 19.
8
Aldo-Keto Reductase Family 1 Member B10 (AKR1B10) overexpression in tumors predicts worse overall survival in hepatocellular carcinoma.醛酮还原酶家族1成员B10(AKR1B10)在肿瘤中的过表达预示着肝细胞癌患者更差的总生存期。
J Cancer. 2019 Aug 27;10(20):4892-4901. doi: 10.7150/jca.32768. eCollection 2019.
9
Diagnostic and Prognostic Potential of AKR1B10 in Human Hepatocellular Carcinoma.AKR1B10在人类肝细胞癌中的诊断和预后潜力
Cancers (Basel). 2019 Apr 5;11(4):486. doi: 10.3390/cancers11040486.
10
AKR1B10 expression predicts response of gastric cancer to neoadjuvant chemotherapy.醛酮还原酶1B10(AKR1B10)的表达可预测胃癌对新辅助化疗的反应。
Oncol Lett. 2019 Jan;17(1):773-780. doi: 10.3892/ol.2018.9705. Epub 2018 Nov 15.