Morphogenetic action of retinoids and estrogens.

Retinoids and estrogens are small lipophilic compounds fulfilling important biological roles in vertebrate development, reproduction and homeostasis. Both types of ligands are regulators of gene transcription by binding to (nuclear) proteins acting as ligand-activatable transcription factors, members of the nuclear receptor gene superfamily. Retinoids and their multiple receptors (RARs/RXRs) are particularly well-known for their role in early development and spermatogenesis, while much less is known about the two estrogen receptors (ERalpha/beta) during development. In this article we describe some of our previous and present work in both areas of research.

[1]  S. Ross,et al.  Vitamin A in epithelial differentiation and skin carcinogenesis. , 2009, Nutrition reviews.

[2]  B. van der Burg,et al.  Retinoic acid hydroxylase (CYP26) is a key enzyme in neuronal differentiation of embryonal carcinoma cells. , 1999, Developmental Biology.

[3]  E. Sonneveld,et al.  Embryonal carcinoma cell lines stably transfected with mRARbeta2-lacZ: sensitive system for measuring levels of active retinoids. , 1999, Experimental cell research.

[4]  A. Durston,et al.  Expression of retinoic acid 4-hydroxylase (CYP26) during mouse and Xenopus laevis embryogenesis , 1999, Mechanisms of Development.

[5]  J. Gustafsson,et al.  Expression of estrogen receptor alpha and beta during mouse embryogenesis , 1999, Mechanisms of Development.

[6]  A D Vethaak,et al.  Development of a stably transfected estrogen receptor-mediated luciferase reporter gene assay in the human T47D breast cancer cell line. , 1999, Toxicological sciences : an official journal of the Society of Toxicology.

[7]  J. Gustafsson,et al.  Generation and reproductive phenotypes of mice lacking estrogen receptor beta. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[8]  T. Pieler,et al.  Regionalized metabolic activity establishes boundaries of retinoic acid signalling , 1998, The EMBO journal.

[9]  J. Corton,et al.  Interaction of Estrogenic Chemicals and Phytoestrogens with Estrogen Receptor β. , 1998, Endocrinology.

[10]  U. Lendahl,et al.  Retinoid-X receptor signalling in the developing spinal cord , 1998, Nature.

[11]  J. Voorhees,et al.  Retinoic acid receptors regulate expression of retinoic acid 4-hydroxylase that specifically inactivates all-trans retinoic acid in human keratinocyte HaCaT cells. , 1998, The Journal of investigative dermatology.

[12]  T. Jessell,et al.  Motor Neuron–Derived Retinoid Signaling Specifies the Subtype Identity of Spinal Motor Neurons , 1998, Cell.

[13]  B. van der Burg,et al.  Human retinoic acid (RA) 4-hydroxylase (CYP26) is highly specific for all-trans-RA and can be induced through RA receptors in human breast and colon carcinoma cells. , 1998, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.

[14]  G. E. Jones,et al.  Retinoic acid as a chemotactic molecule in neuronal development , 1998, International Journal of Developmental Neuroscience.

[15]  R. Krumlauf,et al.  Initiation of Rhombomeric Hoxb4 Expression Requires Induction by Somites and a Retinoid Pathway , 1998, Neuron.

[16]  G. Folkers,et al.  Inhibition of retinoic acid receptor-mediated signalling alters positional identity in the developing hindbrain. , 1998, Development.

[17]  P. Chambon,et al.  Mouse P450RAI (CYP26) Expression and Retinoic Acid-inducible Retinoic Acid Metabolism in F9 Cells Are Regulated by Retinoic Acid Receptor γ and Retinoid X Receptor α* , 1998, The Journal of Biological Chemistry.

[18]  J. Sussenbach,et al.  The role of MAP kinase in TPA-mediated cell cycle arrest of human breast cancer cells , 1998, Oncogene.

[19]  B. van der Burg,et al.  Mitogenic Signaling of Insulin-like Growth Factor I in MCF-7 Human Breast Cancer Cells Requires Phosphatidylinositol 3-Kinase and Is Independent of Mitogen-activated Protein Kinase* , 1997, The Journal of Biological Chemistry.

[20]  E. Mambo,et al.  Estrogen-dependent transcriptional activation and vitellogenin gene memory. , 1997, Molecular endocrinology.

[21]  F. Dilworth,et al.  cDNA Cloning of Human Retinoic Acid-metabolizing Enzyme (hP450RAI) Identifies a Novel Family of Cytochromes P450 (CYP26)* , 1997, The Journal of Biological Chemistry.

[22]  D. Gottlieb,et al.  CYP26, a Novel Mammalian Cytochrome P450, Is Induced by Retinoic Acid and Defines a New Family* , 1997, The Journal of Biological Chemistry.

[23]  B. van der Burg,et al.  Autoinduction of Retinoic Acid Metabolism to Polar Derivatives with Decreased Biological Activity in Retinoic Acid-sensitive, but Not in Retinoic Acid-resistant Human Breast Cancer Cells* , 1997, The Journal of Biological Chemistry.

[24]  Y. Fujii‐Kuriyama,et al.  Metabolic inactivation of retinoic acid by a novel P450 differentially expressed in developing mouse embryos , 1997, The EMBO journal.

[25]  P. Chambon,et al.  Genetic evidence that the retinoid signal is transduced by heterodimeric RXR/RAR functional units during mouse development. , 1997, Development.

[26]  F. Dilworth,et al.  Identification of the Retinoic Acid-inducible All-trans-retinoic Acid 4-Hydroxylase* , 1996, The Journal of Biological Chemistry.

[27]  J. Polman,et al.  ERβ: Identification and characterization of a novel human estrogen receptor , 1996 .

[28]  J. Gustafsson,et al.  Cloning of a novel receptor expressed in rat prostate and ovary. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[29]  Bart,et al.  Cyclin D1 triggers autonomous growth of breast cancer cells by governing cell cycle exit , 1996, Molecular and cellular biology.

[30]  K. Korach,et al.  Alterations of maternal estrogen levels during gestation affect the skeleton of female offspring. , 1996, Endocrinology.

[31]  J. Takatsuka,et al.  Retinoic acid metabolism and inhibition of cell proliferation: an unexpected liaison. , 1996, Cancer research.

[32]  Dirk,et al.  All-trans-4-oxo-retinoic acid: a potent inducer of in vivo proliferation of growth-arrested A spermatogonia in the vitamin A-deficient mouse testis. , 1996, Endocrinology.

[33]  Philippe Kastner,et al.  Nonsteroid nuclear receptors: What Are genetic studies telling us about their role in real life? , 1995, Cell.

[34]  R. Newbold Cellular and molecular effects of developmental exposure to diethylstilbestrol: implications for other environmental estrogens. , 1995, Environmental health perspectives.

[35]  N. Keiding,et al.  Declining semen quality and increasing incidence of testicular cancer: is there a common cause? , 1995, Environmental health perspectives.

[36]  B. Burg,et al.  Differential regulation of AP1 activity by retinoic acid in hormone-dependent and -independent breast cancer cells , 1995, Molecular and Cellular Endocrinology.

[37]  K. Sulik,et al.  Teratogenicity of low doses of all-trans retinoic acid in presomite mouse embryos. , 1995, Teratology.

[38]  K. Nelson,et al.  Exposure to diethylstilbestrol during a critical developmental period of the mouse reproductive tract leads to persistent induction of two estrogen-regulated genes. , 1994, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.

[39]  K. Korach,et al.  Alteration of reproductive function but not prenatal sexual development after insertional disruption of the mouse estrogen receptor gene. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[40]  G. Folkers,et al.  The retinoid ligand 4-oxo-retinoic acid is a highly active modulator of positional specification , 1993, Nature.

[41]  A. Soto,et al.  Developmental effects of endocrine-disrupting chemicals in wildlife and humans. , 1993, Environmental health perspectives.

[42]  B. Burg,et al.  Retinoic acid resistance of estradiol-independent breast cancer cells coincides with diminished retinoic acid receptor function , 1993, Molecular and Cellular Endocrinology.

[43]  J. van Dun,et al.  Effects of liarozole, a new antitumoral compound, on retinoic acid-induced inhibition of cell growth and on retinoic acid metabolism in MCF-7 human breast cancer cells. , 1992, Cancer research.

[44]  M. J. Coon,et al.  Role of isozymes of rabbit microsomal cytochrome P-450 in the metabolism of retinoic acid, retinol, and retinal. , 1992, Molecular pharmacology.

[45]  D W Nebert,et al.  Proposed role of drug-metabolizing enzymes: regulation of steady state levels of the ligands that effect growth, homeostasis, differentiation, and neuroendocrine functions. , 1991, Molecular endocrinology.

[46]  P. Chambon,et al.  Retinoic acid receptors and cellular retinoid binding proteins. I. A systematic study of their differential pattern of transcription during mouse organogenesis. , 1990, Development.

[47]  B. van der Burg,et al.  Stimulation of TPA-responsive element activity by a cooperative action of insulin and estrogen in human breast cancer cells. , 1990, Molecular endocrinology.

[48]  P. Chambon,et al.  Differential expression of genes encoding α, β and γ retinoic acid receptors and CRABP in the developing limbs of the mouse , 1989, Nature.

[49]  H. Hendriks,et al.  Retinoic acid causes an anteroposterior transformation in the developing central nervous system , 1989, Nature.

[50]  B. Burg,et al.  Direct effects of estrogen on c-fos and c-myc protooncogene expression and cellular proliferation in human breast cancer cells , 1989, Molecular and Cellular Endocrinology.

[51]  G. Van Nijen,et al.  Ketoconazole inhibits the in vitro and in vivo metabolism of all-trans-retinoic acid. , 1988, The Journal of pharmacology and experimental therapeutics.

[52]  M. Blankenstein,et al.  Mitogenic stimulation of human breast cancer cells in a growth factor‐defined medium: Synergistic action of insulin and estrogen , 1988, Journal of cellular physiology.

[53]  A. Herbst,et al.  Adenocarcinoma of the vagina. Association of maternal stilbestrol therapy with tumor appearance in young women. , 1971, The New England journal of medicine.

[54]  M. Petkovich,et al.  A molecular basis for retinoic acid-induced axial truncation. , 1999, Developmental biology.

[55]  A. Ekbom,et al.  Growing evidence that several human cancers may originate in utero. , 1998, Seminars in cancer biology.

[56]  A. Durston,et al.  Retinoids and related signals in early development of the vertebrate central nervous system. , 1998, Current topics in developmental biology.

[57]  A. Durston,et al.  4 Retinoids and Related Signals in Early Development of the Vertebrate Central Nervous System , 1998 .

[58]  J. Corton,et al.  Interaction of estrogenic chemicals and phytoestrogens with estrogen receptor beta. , 1998, Endocrinology.

[59]  I. Gut,et al.  P450 in the rat and man: methods of investigation, substrate specificities and relevance to cancer. , 1994, Xenobiotica; the fate of foreign compounds in biological systems.

[60]  S. Pemrick,et al.  The retinoid receptors. , 1994, Leukemia.

[61]  Pemrick Sm,et al.  The retinoid receptors. , 1994 .

[62]  C. Lieber,et al.  Increased hepatic retinal dehydrogenase activity after phenobarbital and ethanol administration. , 1989, Biochemical pharmacology.

[63]  M. Sporn,et al.  Cellular biology and biochem-istry of the retinoids , 1984 .

[64]  Bart,et al.  Printed in U.S.A. Copyright © 1999 by The Endocrine Society Ontogeny of Estrogen Receptor- � Expression in Rat Testis* , 2022 .

[65]  J. Gustafsson,et al.  Cloning of a novel estrogen receptor expressed in rat prostate and ovary , 2022 .