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    AKR1C4 aldo-keto reductase family 1 member C4 [ Homo sapiens (human) ]

    Gene ID: 1109, updated on 11-Apr-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    the present study suggests that AKR1C1, AKR1C2, AKR1C3, and AKR1C4 are closely associated with drug resistance to both CDDP and 5FU, and that mefenamic acid, an inhibitor of AKR1C, restores sensitivity through inhibition of drug-resistance in human cancer cells.

    Mefenamic acid enhances anticancer drug sensitivity via inhibition of aldo-keto reductase 1C enzyme activity.
    Shiiba M, Yamagami H, Yamamoto A, Minakawa Y, Okamoto A, Kasamatsu A, Sakamoto Y, Uzawa K, Takiguchi Y, Tanzawa H.

    04/22/2017
    Studies indicate that mutations in aldo-keto reductase family 1 (AKR1) enzymes AKR1C1 and AKR1C4 are responsible for sexual development dysgenesis and mutations in AKR1D1 are causative in bile-acid deficiency.

    Role of aldo-keto reductase family 1 (AKR1) enzymes in human steroid metabolism.
    Rižner TL, Penning TM., Free PMC Article

    08/30/2014
    In women only, SNPs in AKR1C4 reduced the likelihood of having exhibited paranoid ideation by circa 60%.

    Polymorphisms in AKR1C4 and HSD3B2 and differences in serum DHEAS and progesterone are associated with paranoid ideation during mania or hypomania in bipolar disorder.
    Johansson AG, Nikamo P, Schalling M, Landén M.

    01/26/2013
    Low progesterone levels and a cystine to serine change at position 145 in AKR1C4 gene are associated with manic/hypomanic irritability in males

    AKR1C4 gene variant associated with low euthymic serum progesterone and a history of mood irritability in males with bipolar disorder.
    Johansson AG, Nikamo P, Schalling M, Landén M.

    11/12/2011
    role of AKR1C4 in the metabolism of testosterone and progesterone via the 5beta-reductase pathway.

    Stereospecific reduction of 5β-reduced steroids by human ketosteroid reductases of the AKR (aldo-keto reductase) superfamily: role of AKR1C1-AKR1C4 in the metabolism of testosterone and progesterone via the 5β-reductase pathway.
    Jin Y, Mesaros AC, Blair IA, Penning TM., Free PMC Article

    09/3/2011
    Observational study and genome-wide association study of gene-disease association. (HuGE Navigator)

    Human variation in alcohol response is influenced by variation in neuronal signaling genes.
    Joslyn G, Ravindranathan A, Brush G, Schuckit M, White RL.

    04/7/2010
    Observational study of gene-disease association and gene-environment interaction. (HuGE Navigator)

    Polymorphisms in innate immunity genes and lung cancer risk in Xuanwei, China.
    Shen M, Vermeulen R, Rajaraman P, Menashe I, He X, Chapman RS, Yeager M, Thomas G, Burdett L, Hutchinson A, Yuenger J, Chanock S, Lan Q., Free PMC Article

    04/7/2010
    Structure determination of human AKR1C4 and homology modelling of AKR1D1 followed by docking experiments were used to explore active site geometries.

    Structure-activity relationships of human AKR-type oxidoreductases involved in bile acid synthesis: AKR1D1 and AKR1C4.
    Lee WH, Lukacik P, Guo K, Ugochukwu E, Kavanagh KL, Marsden B, Oppermann U.

    01/21/2010
    Observational study of gene-disease association. (HuGE Navigator)See all PubMed (6) articles

    Genetic variation in the estrogen metabolic pathway and mammographic density as an intermediate phenotype of breast cancer.
    Li J, Eriksson L, Humphreys K, Czene K, Liu J, Tamimi RM, Lindström S, Hunter DJ, Vachon CM, Couch FJ, Scott CG, Lagiou P, Hall P.

    Genetic susceptibility to distinct bladder cancer subphenotypes.
    Guey LT, García-Closas M, Murta-Nascimento C, Lloreta J, Palencia L, Kogevinas M, Rothman N, Vellalta G, Calle ML, Marenne G, Tardón A, Carrato A, García-Closas R, Serra C, Silverman DT, Chanock S, Real FX, Malats N, EPICURO/Spanish Bladder Cancer Study investigators.

    PTEN identified as important risk factor of chronic obstructive pulmonary disease.
    Hosgood HD 3rd, Menashe I, He X, Chanock S, Lan Q.

    Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway.
    Hosgood HD 3rd, Menashe I, Shen M, Yeager M, Yuenger J, Rajaraman P, He X, Chatterjee N, Caporaso NE, Zhu Y, Chanock SJ, Zheng T, Lan Q.

    An estrogen metabolism-related polymorphism of the 17-alpha HSD gene is associated with perimenopausal body mass index.
    Tempfer CB, Huber C, Huber JC, Schneeberger C, Bentz EK, Hefler LA.

    A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.
    Grupe A, Li Y, Rowland C, Nowotny P, Hinrichs AL, Smemo S, Kauwe JS, Maxwell TJ, Cherny S, Doil L, Tacey K, van Luchene R, Myers A, Wavrant-De Vrièze F, Kaleem M, Hollingworth P, Jehu L, Foy C, Archer N, Hamilton G, Holmans P, Morris CM, Catanese J, Sninsky J, White TJ, Powell J, Hardy J, O'Donovan M, Lovestone S, Jones L, Morris JC, Thal L, Owen M, Williams J, Goate A.

    03/13/2008
    Clinical trial of gene-disease association. (HuGE Navigator)

    Polymorphisms in genes involved in estrogen and progesterone metabolism and mammographic density changes in women randomized to postmenopausal hormone therapy: results from a pilot study.
    Lord SJ, Mack WJ, Van Den Berg D, Pike MC, Ingles SA, Haiman CA, Wang W, Parisky YR, Hodis HN, Ursin G., Free PMC Article

    03/13/2008
    Impact of mirtazapine on the activity of a key neurosteroidogenic enzyme, the 3alpha-hydroxysteroid dehydrogenase (3alpha-HSD), and on the levels of neuroactive steroids in relation to clinical response in depression.

    Influence of mirtazapine on plasma concentrations of neuroactive steroids in major depression and on 3alpha-hydroxysteroid dehydrogenase activity.
    Schüle C, Romeo E, Uzunov DP, Eser D, di Michele F, Baghai TC, Pasini A, Schwarz M, Kempter H, Rupprecht R.

    01/21/2010
    the expression level of DD4 mRNA is cooperatively regulated by the amounts of HNF-1 alpha, HNF-4 alpha and HNF-4 gamma.

    Hepatocyte nuclear factor-4 alpha/gamma and hepatocyte nuclear factor-1 alpha as causal factors of interindividual difference in the expression of human dihydrodiol dehydrogenase 4 mRNA in human livers.
    Ozeki T, Takahashi Y, Nakayama K, Funayama M, Nagashima K, Kodama T, Kamataki T.

    01/21/2010
    Taken together, we conclude that the cell-type-specific expression of DD4 mRNA is regulated by vHNF-1-C.

    Hepatocyte nuclear factor (HNF)-4 alpha/gamma, HNF-1 alpha, and vHNF-1 regulate the cell-specific expression of the human dihydrodiol dehydrogenase (DD)4/AKR1C4 gene.
    Ozeki T, Takahashi Y, Nakayama K, Kamataki T.

    01/21/2010
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