-
1
-
-
0030925341
-
Molecular endocrinology of hydroxysteroid dehydrogenases
-
DOI 10.1210/er.18.3.281
-
Penning, T.M. Molecular endocrinology of hydroxysteroid dehydrogenases. Endocr. Rev., 1997, 18, 281-305. (Pubitemid 27246879)
-
(1997)
Endocrine Reviews
, vol.18
, Issue.3
, pp. 281-305
-
-
Penning, T.M.1
-
2
-
-
34547692874
-
Human aldo-keto reductases: Function, gene regulation, and single nucleotide polymorphisms
-
DOI 10.1016/j.abb.2007.04.024, PII S0003986107002226
-
Penning, T.M.; Drury, J.E. Human aldo-keto reductases: function, gene regulation, and single nucleotide polymorphisms. Arch. Biochem. Biophys., 2007, 464, 241-250. (Pubitemid 47214569)
-
(2007)
Archives of Biochemistry and Biophysics
, vol.464
, Issue.2
, pp. 241-250
-
-
Penning, T.M.1
Drury, J.E.2
-
3
-
-
61649103983
-
Steroid hormone transforming aldo-keto reductases and cancer
-
Penning, T.M.; Byrns, M.C. Steroid hormone transforming aldo-keto reductases and cancer. Ann. N. Y. Acad. Sci., 2009, 1155, 33-42.
-
(2009)
Ann. N. Y. Acad. Sci.
, vol.1155
, pp. 33-42
-
-
Penning, T.M.1
Byrns, M.C.2
-
4
-
-
0034287545
-
Human 3alpha-hydroxysteroid dehydrogenase isoforms (AKR1C1-AKR1C4) of the aldo-keto reductase superfamily: Functional plasticity and tissue distribution reveals roles in the inactivation and formation of male and female sex hormones
-
Penning, T.M.; Burczynski, M.E.; Jez, J.M.; Hung, C.F.; Lin, H.K.; Ma, H.; Moore, M.; Palackal, N.; Ratnam, K. Human 3alpha-hydroxysteroid dehydrogenase isoforms (AKR1C1-AKR1C4) of the aldo-keto reductase superfamily: functional plasticity and tissue distribution reveals roles in the inactivation and formation of male and female sex hormones. Biochem. J., 2000, 351, 67-77.
-
(2000)
Biochem. J.
, vol.351
, pp. 67-77
-
-
Penning, T.M.1
Burczynski, M.E.2
Jez, J.M.3
Hung, C.F.4
Lin, H.K.5
Ma, H.6
Moore, M.7
Palackal, N.8
Ratnam, K.9
-
5
-
-
0037328450
-
The aldo-keto reductase superfamily homepage
-
DOI 10.1016/S0009-2797(02)00193-X, PII S000927970200193X
-
Hyndman, D.; Bauman, D.R.; Heredia, V.V.; Penning, T.M. The aldo-keto reductase superfamily homepage. Chem. Biol. Interact., 2003, 143-144, 621-631. (Pubitemid 36246464)
-
(2003)
Chemico-Biological Interactions
, vol.143-144
, pp. 621-631
-
-
Hyndman, D.1
Bauman, D.R.2
Heredia, V.V.3
Penning, T.M.4
-
6
-
-
33644909044
-
AKR1C1 and AKR1C3 may determine progesterone and estrogen ratios in endometrial cancer
-
Lani-nik Ri ner, T.; muc, T.; Rupreht, R.; inkovec, J.; Penning, T.M. AKR1C1 and AKR1C3 may determine progesterone and estrogen ratios in endometrial cancer. Mol. Cell. Endocrinol., 2006, 248, 126-135.
-
(2006)
Mol. Cell. Endocrinol.
, vol.248
, pp. 126-135
-
-
Lani-nik Ri Ner, T.1
Muc, T.2
Rupreht, R.3
Inkovec, J.4
Penning, T.M.5
-
7
-
-
12144249551
-
Expression and activity of steroid aldoketoreductases 1C in omental adipose tissue are positive correlates of adiposity in women
-
DOI 10.1152/ajpendo.00312.2004
-
Blouin, K.; Blanchette, S.; Richard, C.; Dupont, P.; Luu-The, V.; Tchernof, A. Expression and activity of steroid aldoketoreductases 1C in omental adipose tissue are positive correlates of adiposity in women. Am. J. Physiol. Endocrinol. Metab., 2005, 288, E398-404. (Pubitemid 40110649)
-
(2005)
American Journal of Physiology - Endocrinology and Metabolism
, vol.288
, Issue.2
-
-
Blouin, K.1
Blanchette, S.2
Richard, C.3
Dupont, P.4
Luu-The, V.5
Tchernof, A.6
-
8
-
-
33644926096
-
Deoxycorticosterone inactivation by AKR1C3 in human mineralocorticoid target tissues
-
Sharma, K.K.; Lindqvist, A.; Zhou, X.J.; Auchus, R.J.; Penning, T.M.; Andersson, S. Deoxycorticosterone inactivation by AKR1C3 in human mineralocorticoid target tissues. Mol. Cell. Endocrinol., 2006, 248, 79-86.
-
(2006)
Mol. Cell. Endocrinol.
, vol.248
, pp. 79-86
-
-
Sharma, K.K.1
Lindqvist, A.2
Zhou, X.J.3
Auchus, R.J.4
Penning, T.M.5
Andersson, S.6
-
9
-
-
0037661059
-
Human type 3 3alpha-hydroxysteroid dehydrogenase (aldo-keto reductase 1C2) and androgen metabolism in prostate cells
-
Lani-nik Ri ner, T.; Lin, H.K.; Peehl, D.M.; Steckelbroeck, S.; Bauman, D.R.; Penning, T.M. Human type 3 3alpha-hydroxysteroid dehydrogenase (aldo-keto reductase 1C2) and androgen metabolism in prostate cells. Endocrinology, 2003, 144, 2922-2932.
-
(2003)
Endocrinology
, vol.144
, pp. 2922-2932
-
-
Lani-nik Ri Ner, T.1
Lin, H.K.2
Peehl, D.M.3
Steckelbroeck, S.4
Bauman, D.R.5
Penning, T.M.6
-
10
-
-
1642305724
-
Human cytosolic 3α-hydroxysteroid dehydrogenases of the aldo-keto reductase superfamily display significant 3β-hydroxysteroid dehydrogenase activity: Implications for steroid hormone metabolism and action
-
DOI 10.1074/jbc.M313308200
-
Steckelbroeck, S.; Jin, Y.; Gopishetty, S.; Oyesanmi, B.; Penning, T.M. Human cytosolic 3alpha-hydroxysteroid dehydrogenases of the aldo-keto reductase superfamily display significant 3beta-hydroxysteroid dehydrogenase activity: implications for steroid hormone metabolism and action. J. Biol. Chem., 2004, 279, 10784-10795. (Pubitemid 38379543)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.11
, pp. 10784-10795
-
-
Steckelbroeck, S.1
Jin, Y.2
Gopishetty, S.3
Oyesanmi, B.4
Penning, T.M.5
-
11
-
-
0034836548
-
Metabolic conversion as a pre-receptor control mechanism for lipophilic hormones
-
DOI 10.1046/j.1432-1327.2001.02359.x
-
Nobel, S.; Abrahmsen, L.; Oppermann, U. Metabolic conversion as a prereceptor control mechanism for lipophilic hormones. Eur. J. Biochem., 2001, 268, 4113-4125. (Pubitemid 32862871)
-
(2001)
European Journal of Biochemistry
, vol.268
, Issue.15
, pp. 4113-4125
-
-
Nobel, S.1
Abrahmsen, L.2
Oppermann, U.3
-
12
-
-
0001429526
-
Characteristics of a highly labile human type 5 17β-hydroxysteroid dehydrogenase
-
DOI 10.1210/en.140.2.568
-
Dufort, I.; Rheault, P.; Huang, X.F.; Soucy, P.; Luu-The, V. Characteristics of a highly labile human type 5 17beta-hydroxysteroid dehydrogenase. Endocrinology, 1999, 140, 568-574. (Pubitemid 29058186)
-
(1999)
Endocrinology
, vol.140
, Issue.2
, pp. 568-574
-
-
Dufort, I.1
Rheault, P.2
Huang, X.-F.3
Soucy, P.4
Luu-The, V.5
-
13
-
-
0035093784
-
Human types 1 and 3 3α-hydroxysteroid dehydrogenases: Differential lability and tissue distribution
-
DOI 10.1210/jc.86.2.841
-
Dufort, I.; Labrie, F.; Luu-The, V. Human types 1 and 3 3-alphahydroxysteroid dehydrogenases: differential lability and tissue distribution. J. Clin. Endocrinol. Metab., 2001, 86, 841-846. (Pubitemid 32208285)
-
(2001)
Journal of Clinical Endocrinology and Metabolism
, vol.86
, Issue.2
, pp. 841-846
-
-
Dufort, I.1
Labrie, F.2
Luu-The, V.3
-
14
-
-
1542725957
-
Structure-function of human 3α-hydroxysteroid dehydrogenases: Genes and proteins
-
DOI 10.1016/j.mce.2003.11.006, PII S0303720703005057
-
Penning, T.M.; Jin, Y.; Steckelbroeck, S.; Lani-nik Ri ner, T.; Lewis, M. Structure-function of human 3-alpha-hydroxysteroid dehydrogenases: genes and proteins. Mol. Cell. Endocrinol., 2004, 215, 63-72. (Pubitemid 38337424)
-
(2004)
Molecular and Cellular Endocrinology
, vol.215
, Issue.1-2
, pp. 63-72
-
-
Penning, T.M.1
Jin, Y.2
Steckelbroeck, S.3
Rizner, T.L.4
Lewis, M.5
-
15
-
-
0034099083
-
Hormonal carcinogenesis
-
Henderson, B.E.; Feigelson, H.S. Hormonal carcinogenesis. Carcinogenesis, 2000, 21, 427-433. (Pubitemid 30137927)
-
(2000)
Carcinogenesis
, vol.21
, Issue.3
, pp. 427-433
-
-
Henderson, B.E.1
Feigelson, H.S.2
-
16
-
-
60249095065
-
Disturbed estrogen and progesterone action in ovarian endometriosis
-
muc, T.; Hevir, N.; Ribic-Pucelj, M.; Husen, B.; Thole, H.; Lani-nik Ri ner, T. Disturbed estrogen and progesterone action in ovarian endometriosis. Mol. Cell. Endocrinol., 2009, 301, 59-64.
-
(2009)
Mol. Cell. Endocrinol.
, vol.301
, pp. 59-64
-
-
Muc, T.1
Hevir, N.2
Ribic-Pucelj, M.3
Husen, B.4
Thole, H.5
Lani-nik Ri Ner, T.6
-
17
-
-
5644227416
-
Selective loss of AKR1C1 and AKR1C2 in breast cancer and their potential effect on progesterone signaling
-
DOI 10.1158/0008-5472.CAN-04-1608
-
Ji, Q.; Aoyama, C.; Nien, Y.; Liu, P.I.; Chen, P.K.; Chang, L.; Stanczyk, F.Z.; Stolz, A. Selective loss of AKR1C1 and AKR1C2 in breast cancer and their potential effect on progesterone signaling. Cancer Res., 2004, 64, 7610-7617. (Pubitemid 39372107)
-
(2004)
Cancer Research
, vol.64
, Issue.20
, pp. 7610-7617
-
-
Ji, Q.1
Aoyama, C.2
Nien, Y.-D.3
Liu, P.I.4
Chen, P.K.5
Chang, L.6
Stanczyk, F.Z.7
Stolz, A.8
-
18
-
-
0037324845
-
Selective and potent inhibitors of human 20α-hydroxysteroid dehydrogenase (AKR1C1) that metabolizes neurosteroids derived from progesterone
-
DOI 10.1016/S0009-2797(02)00206-5, PII S0009279702002065
-
Higaki, Y.; Usami, N.; Shintani, S.; Ishikura, S.; El-Kabbani, O.; Hara, A. Selective and potent inhibitors of human 20alpha-hydroxysteroid dehydrogenase (AKR1C1) that metabolizes neurosteroids derived from progesterone. Chem. Biol. Interact., 2003, 143-144, 503-513. (Pubitemid 36253599)
-
(2003)
Chemico-Biological Interactions
, vol.143-144
, pp. 503-513
-
-
Higaki, Y.1
Usami, N.2
Shintani, S.3
Ishikura, S.4
El-Kabbani, O.5
Hara, A.6
-
19
-
-
0036547847
-
Substrate specificity of human 3(20)α-hydroxysteroid dehydrogenase for neurosteroids and its inhibition by benzodiazepines
-
DOI 10.1248/bpb.25.441
-
Usami, N.; Yamamoto, T.; Shintani, S.; Ishikura, S.; Higaki, Y.; Katagiri, Y.; Hara, A. Substrate specificity of human 3(20)alpha-hydroxysteroid dehydrogenase for neurosteroids and its inhibition by benzodiazepines. Biol. Pharm. Bull., 2002, 25, 441-445. (Pubitemid 40044660)
-
(2002)
Biological and Pharmaceutical Bulletin
, vol.25
, Issue.4
, pp. 441-445
-
-
Usami, N.1
Yamamoto, T.2
Shintani, S.3
Higaki, Y.4
Ishikura, S.5
Katagiri, Y.6
Hara, A.7
-
20
-
-
45049086572
-
AKR1C2 and AKR1C3 mediated prostaglandin D2 metabolism augments the PI3K/Akt proliferative signaling pathway in human prostate cancer cells
-
Wang, S.; Yang, Q.; Fung, K.; Lin, H. AKR1C2 and AKR1C3 mediated prostaglandin D2 metabolism augments the PI3K/Akt proliferative signaling pathway in human prostate cancer cells. Mol. Cell. Endocrinol., 2008, 289, 60-66.
-
(2008)
Mol. Cell. Endocrinol.
, vol.289
, pp. 60-66
-
-
Wang, S.1
Yang, Q.2
Fung, K.3
Lin, H.4
-
21
-
-
1642357433
-
2 11-Ketoreductase (AKR1C3) in Complex with the Nonsteroidal Anti-Inflammatory Drugs Flufenamic Acid and Indomethacin
-
DOI 10.1158/0008-5472.CAN-03-2847
-
Lovering, A.L.; Ride, J.P.; Bunce, C.M.; Desmond, J.C.; Cummings, S.M.; White, S.A. Crystal structures of prostaglandin D(2) 11-ketoreductase (AKR1C3) in complex with the nonsteroidal anti-inflammatory drugs flufenamic acid and indomethacin. Cancer Res., 2004, 64, 1802-1810. (Pubitemid 38428705)
-
(2004)
Cancer Research
, vol.64
, Issue.5
, pp. 1802-1810
-
-
Lovering, A.L.1
Ride, J.P.2
Bunce, C.M.3
Desmond, J.C.4
Cummings, S.M.5
White, S.A.6
-
22
-
-
0037439967
-
The aldo-keto reductase AKR1C3 is a novel suppressor of cell differentiation that provides a plausible target for the non-cyclooxygenase- dependent antineoplastic actions of nonsteroidal anti-inflammatory drugs
-
Desmond, J.C.; Mountford, J.C.; Drayson, M.T.; Walker, E.A.; Hewison, M.; Ride, J.P.; Luong, Q.T.; Hayden, R.E.; Vanin, E.F.; Bunce, C.M. The aldoketo reductase AKR1C3 is a novel suppressor of cell differentiation that provides a plausible target for the non-cyclooxygenase-dependent antineoplastic actions of nonsteroidal anti-inflammatory drugs. Cancer Res., 2003, 63, 505-512. (Pubitemid 36152514)
-
(2003)
Cancer Research
, vol.63
, Issue.2
, pp. 505-512
-
-
Desmond, J.C.1
Mountford, J.C.2
Drayson, M.T.3
Walker, E.A.4
Hewison, M.5
Ride, J.P.6
Luong, Q.T.7
Hayden, R.E.8
Vanin, E.F.9
Bunce, C.M.10
-
23
-
-
74449092601
-
Aldo-keto reductase 1C3 expression in MCF-7 cells reveals roles in steroid hormone and prostaglandin metabolism that may explain its over-expression in breast cancer
-
Byrns, M.C.; Duan, L.; Lee, S.H.; Blair, I.A.; Penning, T.M. Aldo-keto reductase 1C3 expression in MCF-7 cells reveals roles in steroid hormone and prostaglandin metabolism that may explain its over-expression in breast cancer. J. Steroid Biochem. Mol. Biol., 2010, 118, 177-187.
-
(2010)
J. Steroid Biochem. Mol. Biol.
, vol.118
, pp. 177-187
-
-
Byrns, M.C.1
Duan, L.2
Lee, S.H.3
Blair, I.A.4
Penning, T.M.5
-
24
-
-
33748532180
-
Depot-specific prostaglandin synthesis in human adipose tissue: A novel possible mechanism of adipogenesis
-
DOI 10.1016/j.gene.2006.05.026, PII S0378111906003684
-
Quinkler, M.; Bujalska, I.J.; Tomlinson, J.W.; Smith, D.M.; Stewart, P.M. Depot-specific prostaglandin synthesis in human adipose tissue: a novel possible mechanism of adipogenesis. Gene, 2006, 380, 137-143. (Pubitemid 44363149)
-
(2006)
Gene
, vol.380
, Issue.2
, pp. 137-143
-
-
Quinkler, M.1
Bujalska, I.J.2
Tomlinson, J.W.3
Smith, D.M.4
Stewart, P.M.5
-
25
-
-
65649152952
-
Human cytosolic hydroxysteroid dehydrogenases of the aldo-ketoreductase superfamily catalyze reduction of conjugated steroids: Implications for phase i and phase II steroid hormone metabolism
-
Jin, Y.; Duan, L.; Lee, S.H.; Kloosterboer, H.J.; Blair, I.A.; Penning, T.M. Human cytosolic hydroxysteroid dehydrogenases of the aldo-ketoreductase superfamily catalyze reduction of conjugated steroids: implications for phase I and phase II steroid hormone metabolism. J. Biol. Chem., 2009, 284, 10013-10022.
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 10013-10022
-
-
Jin, Y.1
Duan, L.2
Lee, S.H.3
Kloosterboer, H.J.4
Blair, I.A.5
Penning, T.M.6
-
26
-
-
33644749351
-
Tibolone metabolism in human liver is catalyzed by 3α/3β- hydroxysteroid dehydrogenase activities of the four isoforms of the aldo-keto reductase (AKR)1C subfamily
-
DOI 10.1124/jpet.105.091587
-
Steckelbroeck, S.; Oyesanmi, B.; Jin, Y.; Lee, S.; Kloosterboer, H.J.; Penning, T.M. Tibolone metabolism in human liver is catalyzed by 3alpha/3beta-hydroxysteroid dehydrogenase activities of the four isoforms ofthe aldo-keto reductase (AKR)1C subfamily. J. Pharmacol. Exp. Ther., 2006, 316, 1300-1309. (Pubitemid 43345306)
-
(2006)
Journal of Pharmacology and Experimental Therapeutics
, vol.316
, Issue.3
, pp. 1300-1309
-
-
Steckelbroeck, S.1
Oyesanmi, B.2
Jin, Y.3
Lee, S.-H.4
Kloosterboer, H.J.5
Penning, T.M.6
-
27
-
-
33746739480
-
Expression of dihydrodiol dehydrogenase and resistance to chemotherapy and radiotherapy in adenocarcinoma cells of lung
-
Hung, J.; Chow, K.; Wang, H.; Wang, L. Expression of dihydrodiol dehydrogenase and resistance to chemotherapy and radiotherapy in adenocarcinoma cells of lung. Anticancer Res., 2006, 26, 2949-2955. (Pubitemid 44161785)
-
(2006)
Anticancer Research
, vol.26
, Issue.4 B
, pp. 2949-2955
-
-
Hung, J.-J.1
Chow, K.-C.2
Wang, H.-W.3
Wang, L.-S.4
-
28
-
-
0030821699
-
Comparative anatomy of the aldo-keto reductase superfamily
-
Jez, J.M.; Bennett, M.J.; Schlegel, B.P.; Lewis, M.; Penning, T.M. Comparative anatomy of the aldo-keto reductase superfamily. Biochem. J., 1997, 326 (3), 625-636. (Pubitemid 27438032)
-
(1997)
Biochemical Journal
, vol.326
, Issue.3
, pp. 625-636
-
-
Jez, J.M.1
Bennett, M.J.2
Schlegel, B.P.3
Lewis, M.4
Penning, T.M.5
-
29
-
-
79957933677
-
-
The PyMOL Molecular Graphics System, Version 1.3, Schrödinger, LLC
-
The PyMOL Molecular Graphics System, Version 1.3, Schrödinger, LLC.
-
-
-
-
30
-
-
3042829462
-
Crystal structures of the multispecific 17β-hydroxysteroid dehydrogenase type 5: Critical androgen regulation in human peripheral tissues
-
DOI 10.1210/me.2004-0032
-
Qiu, W.; Zhou, M.; Labrie, F.; Lin, S. Crystal structures of the multispecific 17beta-hydroxysteroid dehydrogenase type 5: critical androgen regulation in human peripheral tissues. Mol. Endocrinol., 2004, 18, 1798-1807. (Pubitemid 38859585)
-
(2004)
Molecular Endocrinology
, vol.18
, Issue.7
, pp. 1798-1807
-
-
Qiu, W.1
Zhou, M.2
Labrie, F.3
Lin, S.-X.4
-
31
-
-
0035964182
-
+ and ursodeoxycholate
-
DOI 10.1021/bi010919a
-
Jin, Y.; Stayrook, S.E.; Albert, R.H.; Palackal, N.T.; Penning, T.M.; Lewis, M. Crystal structure of human type III 3alpha-hydroxysteroid dehydrogenase/bile acid binding protein complexed with NADP(+) and ursodeoxycholate. Biochemistry, 2001, 40, 10161-10168. (Pubitemid 32800122)
-
(2001)
Biochemistry
, vol.40
, Issue.34
, pp. 10161-10168
-
-
Jin, Y.1
Stayrook, S.E.2
Albert, R.H.3
Palackal, N.T.4
Penning, T.M.5
Lewis, M.6
-
32
-
-
0043095539
-
Human 20α-hydroxysteroid dehydrogenase: Crystallographic and site-directed mutagenesis studies lead to the identification of an alternative binding site for C21-steroids
-
DOI 10.1016/S0022-2836(03)00762-9
-
Couture, J.; Legrand, P.; Cantin, L.; Luu-The, V.; Labrie, F.; Breton, R. Human 20alpha-hydroxysteroid dehydrogenase: crystallographic and sitedirected mutagenesis studies lead to the identification of an alternative binding site for C21-steroids. J. Mol. Biol., 2003, 331, 593-604. (Pubitemid 36937148)
-
(2003)
Journal of Molecular Biology
, vol.331
, Issue.3
, pp. 593-604
-
-
Couture, J.-F.1
Legrand, P.2
Cantin, L.3
Luu-The, V.4
Labrie, F.5
Breton, R.6
-
33
-
-
0032502245
-
Mutagenesis of 3α-hydroxysteroid dehydrogenase reveals a 'push -pull' mechanism for proton transfer in aldo-keto reductases
-
DOI 10.1021/bi9723055
-
Schlegel, B.P.; Jez, J.M.; Penning, T.M. Mutagenesis of 3 alphahydroxysteroid dehydrogenase reveals a "push-pull" mechanism for proton transfer in aldo-keto reductases. Biochemistry, 1998, 37, 3538-3548. (Pubitemid 28125582)
-
(1998)
Biochemistry
, vol.37
, Issue.10
, pp. 3538-3548
-
-
Schlegel, B.P.1
Jez, J.M.2
Penning, T.M.3
-
34
-
-
33644923476
-
Inhibitory effects of fluorine-substituted estrogens on the activity of 17betahydroxysteroid dehydrogenases
-
Deluca, D.; Möller, G.; Rosinus, A.; Elger, W.; Hillisch, A.; Adamski, J. Inhibitory effects of fluorine-substituted estrogens on the activity of 17betahydroxysteroid dehydrogenases. Mol. Cell. Endocrinol., 2006, 248, 218-224.
-
(2006)
Mol. Cell. Endocrinol.
, vol.248
, pp. 218-224
-
-
Deluca, D.1
Möller, G.2
Rosinus, A.3
Elger, W.4
Hillisch, A.5
Adamski, J.6
-
35
-
-
0035931291
-
Structure-function aspects and inhibitor design of type 5 17β-hydroxysteroid dehydrogenase (AKR1C3)
-
DOI 10.1016/S0303-7207(00)00426-3, PII S0303720700004263
-
Penning, T.M.; Burczynski, M.E.; Jez, J.M.; Lin, H.K.; Ma, H.; Moore, M.; Ratnam, K.; Palackal, N. Structure-function aspects and inhibitor design of type 5 17beta-hydroxysteroid dehydrogenase (AKR1C3). Mol. Cell. Endocrinol., 2001, 171, 137-149. (Pubitemid 32098208)
-
(2001)
Molecular and Cellular Endocrinology
, vol.171
, Issue.1-2
, pp. 137-149
-
-
Penning, T.M.1
Burczynski, M.E.2
Jez, J.M.3
Lin, H.-K.4
Ma, H.5
Moore, M.6
Ratnam, K.7
Palackal, N.8
-
36
-
-
34247218025
-
Structure-based inhibitor design for an enzyme that binds different steroids: A potent inhibitor for human type 5 17β-hydroxysteroid dehydrogenase
-
DOI 10.1074/jbc.M606784200
-
Qiu, W.; Zhou, M.; Mazumdar, M.; Azzi, A.; Ghanmi, D.; Luu-The, V.; Labrie, F.; Lin, S. Structure-based inhibitor design for an enzyme that binds different steroids: a potent inhibitor for human type 5 17beta-hydroxysteroid dehydrogenase. J. Biol. Chem., 2007, 282, 8368-8379. (Pubitemid 47093565)
-
(2007)
Journal of Biological Chemistry
, vol.282
, Issue.11
, pp. 8368-8379
-
-
Qiu, W.1
Zhou, M.2
Mazumdar, M.3
Azzi, A.4
Ghanmi, D.5
Luu-The, V.6
Labrie, F.7
Lin, S.-X.8
-
37
-
-
60149084693
-
Steroidal lactones as inhibitors of 17beta-hydroxysteroid dehydrogenase type 5: Chemical synthesis, enzyme inhibitory activity, and assessment of estrogenic and androgenic activities
-
Bydal, P.; Luu-The, V.; Labrie, F.; Poirier, D. Steroidal lactones as inhibitors of 17beta-hydroxysteroid dehydrogenase type 5: chemical synthesis, enzyme inhibitory activity, and assessment of estrogenic and androgenic activities. Eur J Med Chem, 2009, 44, 632-644.
-
(2009)
Eur J Med Chem
, vol.44
, pp. 632-644
-
-
Bydal, P.1
Luu-The, V.2
Labrie, F.3
Poirier, D.4
-
38
-
-
11244348953
-
Development of nonsteroidal anti-inflammatory drug analogs and steroid carboxylates selective for human aldo-keto reductase isoforms: Potential antineoplastic agents that work independently of cyclooxygenase isozymes
-
DOI 10.1124/mol.104.006569
-
Bauman, D.R.; Rudnick, S.I.; Szewczuk, L.M.; Jin, Y.; Gopishetty, S.; Penning, T.M. Development of nonsteroidal anti-inflammatory drug analogs and steroid carboxylates selective for human aldo-keto reductase isoforms: potential antineoplastic agents that work independently of cyclooxygenase isozymes. Mol. Pharmacol., 2005, 67, 60-68. (Pubitemid 40069966)
-
(2005)
Molecular Pharmacology
, vol.67
, Issue.1
, pp. 60-68
-
-
Bauman, D.R.1
Rudnick, S.I.2
Szewczuk, L.M.3
Jin, Y.4
Gopishetty, S.5
Penning, T.M.6
-
39
-
-
0035931322
-
Phytoestrogens inhibit human 17β-hydroxysteroid dehydrogenase type 5
-
DOI 10.1016/S0303-7207(00)00422-6, PII S0303720700004226
-
Krazeisen, A.; Breitling, R.; Möller, G.; Adamski, J. Phytoestrogens inhibit human 17beta-hydroxysteroid dehydrogenase type 5. Mol. Cell. Endocrinol., 2001, 171, 151-162. (Pubitemid 32098209)
-
(2001)
Molecular and Cellular Endocrinology
, vol.171
, Issue.1-2
, pp. 151-162
-
-
Krazeisen, A.1
Breitling, R.2
Moller, G.3
Adamski, J.4
-
40
-
-
79957970085
-
-
Weiner, H.; Maser, E.; Lindahl, R.; Plapp, B., Eds.; Purdue University: Purdue
-
Broi, P.; Gobec, S.; Laninik Ri ner; T. In: Enzymology and Molecular Biology of Carbonyl Metabolism 13, Weiner, H.; Maser, E.; Lindahl, R.; Plapp, B., Eds.; Purdue University: Purdue, 2007; pp. 252-262..
-
(2007)
Enzymology and Molecular Biology of Carbonyl Metabolism
, vol.13
, pp. 252-262
-
-
Broi, P.1
Gobec, S.2
Riner, L.T.3
-
41
-
-
33748848304
-
Phytoestrogens as inhibitors of the human progesterone metabolizing enzyme AKR1C1
-
DOI 10.1016/j.mce.2006.08.001, PII S0303720706003807
-
Broi, P.; muc, T.; Gobec, S.; Laninik Ri ner, T. Phytoestrogens as inhibitors of the human progesterone metabolizing enzyme AKR1C1. Mol. Cell. Endocrinol., 2006, 259, 30-42. (Pubitemid 44419585)
-
(2006)
Molecular and Cellular Endocrinology
, vol.259
, Issue.1-2
, pp. 30-42
-
-
Brozic, P.1
Smuc, T.2
Gobec, S.3
Rizner, T.L.4
-
42
-
-
59049099978
-
AKR1C3 as a potential target for the inhibitory effect of dietary flavonoids
-
Skarydová, L.; Zivná, L.; Xiong, G.; Maser, E.; Wsól, V. AKR1C3 as a potential target for the inhibitory effect of dietary flavonoids. Chem. Biol. Interact., 2009, 178, 138-144.
-
(2009)
Chem. Biol. Interact.
, vol.178
, pp. 138-144
-
-
Skarydová, L.1
Zivná, L.2
Xiong, G.3
Maser, E.4
Wsól, V.5
-
43
-
-
0034979805
-
Flavonoid biosynthesis. A colorful model for genetics, biochemistry, cell biology, and biotechnology
-
DOI 10.1104/pp.126.2.485
-
Winkel-Shirley, B. Flavonoid biosynthesis. A colorful model for genetics, biochemistry, cell biology, and biotechnology. Plant Physiol., 2001, 126, 485-493. (Pubitemid 32566604)
-
(2001)
Plant Physiology
, vol.126
, Issue.2
, pp. 485-493
-
-
Winkel-Shirley, B.1
-
44
-
-
29344470062
-
Significance of flavonoids in plant resistance and enhancement of their biosynthesis
-
DOI 10.1055/s-2005-873009
-
Treutter, D. Significance of flavonoids in plant resistance and enhancement of their biosynthesis. Plant Biol (Stuttg), 2005, 7, 581-591. (Pubitemid 43004025)
-
(2005)
Plant Biology
, vol.7
, Issue.6
, pp. 581-591
-
-
Treutter, D.1
-
45
-
-
33744482831
-
Combinatorial biosynthesis of flavones and flavonols
-
Miyahisa, I.; Funa, N.; Ohnishi, Y.; Martens, S.; Moriguchi, T.; Horinouchi, S. Combinatorial biosynthesis of flavones and flavonols in Escherichia coli. Appl. Microbiol. Biotechnol., 2006, 71, 53-58.
-
(2006)
Escherichia Coli. Appl. Microbiol. Biotechnol.
, vol.71
, pp. 53-58
-
-
Miyahisa, I.1
Funa, N.2
Ohnishi, Y.3
Martens, S.4
Moriguchi, T.5
Horinouchi, S.6
-
46
-
-
33644907995
-
Cinnamic acids as new inhibitors of 17beta-hydroxysteroid dehydrogenase type 5 (AKR1C3)
-
Broi, P.; Golob, B.; Gomboc, N.; Laninik Riner, T.; Gobec, S. Cinnamic acids as new inhibitors of 17beta-hydroxysteroid dehydrogenase type 5 (AKR1C3). Mol. Cell. Endocrinol., 2006, 248, 233-235.
-
(2006)
Mol. Cell. Endocrinol.
, vol.248
, pp. 233-235
-
-
Broi, P.1
Golob, B.2
Gomboc, N.3
Laninik Riner, T.4
Gobec, S.5
-
47
-
-
0029130399
-
Cinnamic acid: A natural product with potential use in cancer intervention
-
Liu, L.; Hudgins, W.R.; Shack, S.; Yin, M.Q.; Samid, D. Cinnamic acid: a natural product with potential use in cancer intervention. Int. J. Cancer, 1995, 62, 345-350.
-
(1995)
Int. J. Cancer
, vol.62
, pp. 345-350
-
-
Liu, L.1
Hudgins, W.R.2
Shack, S.3
Yin, M.Q.4
Samid, D.5
-
48
-
-
66349108684
-
AKR1C isoforms represent a novel cellular target for jasmonates alongside their mitochondrial-mediated effects
-
Davies, N.J.; Hayden, R.E.; Simpson, P.J.; Birtwistle, J.; Mayer, K.; Ride, J.P.; Bunce, C.M. AKR1C isoforms represent a novel cellular target for jasmonates alongside their mitochondrial-mediated effects. Cancer Res., 2009, 69, 4769-4775.
-
(2009)
Cancer Res.
, vol.69
, pp. 4769-4775
-
-
Davies, N.J.1
Hayden, R.E.2
Simpson, P.J.3
Birtwistle, J.4
Mayer, K.5
Ride, J.P.6
Bunce, C.M.7
-
49
-
-
64249160631
-
New cyclopentane derivatives as inhibitors of steroid metabolizing enzymes AKR1C1 and AKR1C3
-
tefane, B.; Broi, P.; Vehovc, M.; Laninik Ri ner, T.; Gobec, S. New cyclopentane derivatives as inhibitors of steroid metabolizing enzymes AKR1C1 and AKR1C3. Eur J Med Chem, 2009, 44, 2563-2571.
-
(2009)
Eur J Med Chem
, vol.44
, pp. 2563-2571
-
-
Tefane, B.1
Broi, P.2
Vehovc, M.3
Laninik Ri Ner, T.4
Gobec, S.5
-
50
-
-
0343299437
-
Inhibition of a major NAD(P)-linked oxidoreductase from rat liver cytosol by steroidal and nonsteroidal anti-inflammatory agents and by prostaglandins
-
Penning, T.M.; Talalay, P. Inhibition of a major NAD(P)-linked oxidoreductase from rat liver cytosol by steroidal and nonsteroidal antiinflammatory agents and by prostaglandins. Proc. Natl. Acad. Sci. U.S.A., 1983, 80, 4504-4508. (Pubitemid 13077867)
-
(1983)
Proceedings of the National Academy of Sciences of the United States of America
, vol.80
, Issue.14
, pp. 4504-4508
-
-
Penning, T.M.1
Talalay, P.2
-
51
-
-
0032007110
-
3
-
DOI 10.1016/S0145-2126(97)00156-2, PII S0145212697001562
-
Sokoloski, J.A.; Sartorelli, A.C. Induction of the differentiation of HL-60 promyelocytic leukemia cells by nonsteroidal anti-inflammatory agents in combination with low levels of vitamin D3. Leuk. Res., 1998, 22, 153-161. (Pubitemid 28185346)
-
(1998)
Leukemia Research
, vol.22
, Issue.2
, pp. 153-161
-
-
Sokoloski, J.A.1
Sartorelli, A.C.2
-
52
-
-
0029186022
-
Prediction of the coding sequences of unidentified human genes. III. the coding sequences of 40 new genes (KIAA0081-KIAA0120) deduced by analysis of cDNA clones from human cell line KG-1
-
Nagase, T.; Miyajima, N.; Tanaka, A.; Sazuka, T.; Seki, N.; Sato, S.; Tabata, S.; Ishikawa, K.; Kawarabayasi, Y.; Kotani, H.; et al. Prediction of the coding sequences of unidentified human genes. III. The coding sequences of 40 new genes (KIAA0081-KIAA0120) deduced by analysis of cDNA clones from human cell line KG-1. DNA Res., 1995, 2, 37-43.
-
(1995)
DNA Res.
, vol.2
, pp. 37-43
-
-
Nagase, T.1
Miyajima, N.2
Tanaka, A.3
Sazuka, T.4
Seki, N.5
Sato, S.6
Tabata, S.7
Ishikawa, K.8
Kawarabayasi, Y.9
Kotani, H.10
-
53
-
-
27644575900
-
Indolyl esters and amides related to indomethacin are selective COX-2 inhibitors
-
DOI 10.1016/j.bmc.2005.07.073, PII S0968089605007327
-
Kalgutkar, A.S.; Crews, B.C.; Saleh, S.; Prudhomme, D.; Marnett, L.J. Indolyl esters and amides related to indomethacin are selective COX-2 inhibitors. Bioorg. Med. Chem., 2005, 13, 6810-6822. (Pubitemid 41571227)
-
(2005)
Bioorganic and Medicinal Chemistry
, vol.13
, Issue.24
, pp. 6810-6822
-
-
Kalgutkar, A.S.1
Crews, B.C.2
Saleh, S.3
Prudhomme, D.4
Marnett, L.J.5
-
54
-
-
59049089110
-
Type 5 17beta-hydroxysteroid dehydrogenase/prostaglandin F synthase (AKR1C3): Role in breast cancer and inhibition by non-steroidal anti-inflammatory drug analogs
-
Byrns, M.C.; Penning, T.M. Type 5 17beta-hydroxysteroid dehydrogenase/prostaglandin F synthase (AKR1C3): role in breast cancer and inhibition by non-steroidal anti-inflammatory drug analogs. Chem. Biol. Interact., 2009, 178, 221-227.
-
(2009)
Chem. Biol. Interact.
, vol.178
, pp. 221-227
-
-
Byrns, M.C.1
Penning, T.M.2
-
55
-
-
37349047898
-
An indomethacin analogue, N-(4-chlorobenzoyl)-melatonin, is a selective inhibitor of aldo-keto reductase 1C3 (type 2 3α-HSD, type 5 17β-HSD, and prostaglandin F synthase), a potential target for the treatment of hormone dependent and hormone independent malignancies
-
DOI 10.1016/j.bcp.2007.09.008, PII S0006295207006119
-
Byrns, M.C.; Steckelbroeck, S.; Penning, T.M. An indomethacin analogue, N-(4-chlorobenzoyl)-melatonin, is a selective inhibitor of aldo-keto reductase 1C3 (type 2 3alpha-HSD, type 5 17beta-HSD, and prostaglandin F synthase), a potential target for the treatment of hormone dependent and hormone independent malignancies. Biochem. Pharmacol., 2008, 75, 484-493. (Pubitemid 350298472)
-
(2008)
Biochemical Pharmacology
, vol.75
, Issue.2
, pp. 484-493
-
-
Byrns, M.C.1
Steckelbroeck, S.2
Penning, T.M.3
-
56
-
-
37349053079
-
A salicylic acid-based analogue discovered from virtual screening as a potent inhibitor of human 20α-hydroxysteroid dehydrogenase
-
DOI 10.2174/157340607782360399
-
Dhagat, U.; Carbone, V.; Chung, R.P.; Matsunaga, T.; Endo, S.; Hara, A.; El-Kabbani, O. A salicylic acid-based analogue discovered from virtual screening as a potent inhibitor of human 20alpha-hydroxysteroid dehydrogenase. Med Chem, 2007, 3, 546-550. (Pubitemid 350303069)
-
(2007)
Medicinal Chemistry
, vol.3
, Issue.6
, pp. 546-550
-
-
Dhagat, U.1
Carbone, V.2
Chung, R.P.T.3
Matsunaga, T.4
Endo, S.5
Hara, A.6
El-Kabbani, O.7
-
57
-
-
26844480987
-
Nonsteroidal anti-inflammatory drugs and their analogues as inhibitors of aldo-keto reductase AKR1C3: New lead compounds for the development of anticancer agents
-
DOI 10.1016/j.bmcl.2005.08.063, PII S0960894X05010917
-
Gobec, S.; Broi, P.; Laninik Ri ner, T. Nonsteroidal anti-inflammatory drugs and their analogues as inhibitors of aldo-keto reductase AKR1C3: new lead compounds for the development of anticancer agents. Bioorg. Med. Chem. Lett., 2005, 15, 5170-5175. (Pubitemid 41463641)
-
(2005)
Bioorganic and Medicinal Chemistry Letters
, vol.15
, Issue.23
, pp. 5170-5175
-
-
Gobec, S.1
Brozic, P.2
Rizner, T.L.3
-
58
-
-
0032573601
-
Identification of a retinoic acid responsive aldoketoreductase expressed in HL60 leukaemic cells
-
DOI 10.1016/S0014-5793(98)01435-5, PII S0014579398014355
-
Mills, K.I.; Gilkes, A.F.; Sweeney, M.; Choudhry, M.A.; Woodgate, L.J.; Bunce, C.M.; Brown, G.; Burnett, A.K. Identification of a retinoic acid responsive aldoketoreductase expressed in HL60 leukaemic cells. FEBS Lett., 1998, 440, 158-162. (Pubitemid 28558756)
-
(1998)
FEBS Letters
, vol.440
, Issue.1-2
, pp. 158-162
-
-
Mills, K.I.1
Gilkes, A.F.2
Sweeney, M.3
Choudhry, M.A.4
Woodgate, L.J.5
Bunce, C.M.6
Brown, G.7
Burnett, A.K.8
-
59
-
-
59049099037
-
Derivatives of pyrimidine, phthalimide and anthranilic acid as inhibitors of human hydroxysteroid dehydrogenase AKR1C1
-
Bro ic, P.; Cesar, J.; Kova, A.; Davies, M.; Johnson, A.P.; Fishwick, C.W.G.; Laninik Ri ner, T.; Gobec, S. Derivatives of pyrimidine, phthalimide and anthranilic acid as inhibitors of human hydroxysteroid dehydrogenase AKR1C1. Chem. Biol. Interact., 2009, 178, 158-164.
-
(2009)
Chem. Biol. Interact.
, vol.178
, pp. 158-164
-
-
Bro Ic, P.1
Cesar, J.2
Kova, A.3
Davies, M.4
Johnson, A.P.5
Fishwick, C.W.G.6
Laninik Ri Ner, T.7
Gobec, S.8
-
60
-
-
49449097049
-
Selectivity determinants of inhibitor binding to human 20alpha-hydroxysteroid dehydrogenase: Crystal structure of the enzyme in ternary complex with coenzyme and the potent inhibitor 3,5-dichlorosalicylic acid
-
Dhagat, U.; Endo, S.; Sumii, R.; Hara, A.; El-Kabbani, O. Selectivity determinants of inhibitor binding to human 20alpha-hydroxysteroid dehydrogenase: crystal structure of the enzyme in ternary complex with coenzyme and the potent inhibitor 3,5-dichlorosalicylic acid. J. Med. Chem., 2008, 51, 4844-4848.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 4844-4848
-
-
Dhagat, U.1
Endo, S.2
Sumii, R.3
Hara, A.4
El-Kabbani, O.5
-
61
-
-
60249087561
-
Discovery of new inhibitors of aldo-keto reductase 1C1 by structure-based virtual screening
-
Broi, P.; Turk, S.; Laninik Riner, T.; Gobec, S. Discovery of new inhibitors of aldo-keto reductase 1C1 by structure-based virtual screening. Mol. Cell. Endocrinol., 2009, 301, 245-250.
-
(2009)
Mol. Cell. Endocrinol.
, vol.301
, pp. 245-250
-
-
Broi, P.1
Turk, S.2
Laninik Riner, T.3
Gobec, S.4
-
62
-
-
66249105304
-
Structure-guided design, synthesis, and evaluation of salicylic acid-based inhibitors targeting a selectivity pocket in the active site of human 20alpha-hydroxysteroid dehydrogenase (AKR1C1)
-
El-Kabbani, O.; Scammells, P.J.; Gosling, J.; Dhagat, U.; Endo, S.; Matsunaga, T.; Soda, M.; Hara, A. Structure-guided design, synthesis, and evaluation of salicylic acid-based inhibitors targeting a selectivity pocket in the active site of human 20alpha-hydroxysteroid dehydrogenase (AKR1C1). J. Med. Chem., 2009, 52, 3259-3264.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 3259-3264
-
-
El-Kabbani, O.1
Scammells, P.J.2
Gosling, J.3
Dhagat, U.4
Endo, S.5
Matsunaga, T.6
Soda, M.7
Hara, A.8
|