Retinoic acid receptors α, β and γ, and cellular retinol binding protein-I expression in breast fibrocystic disease and cancer (817 views)
Eur J Endocrinol (ISSN: 0804-4643), 1997 Oct; 137(4): 410-414.
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Paper type: Journal Article,
Impact factor: 1.968, 5-year impact factor: 3.325
Url: http://www.scopus.com/inward/record.url?eid=2-s2.0-0030869575&partnerID=40&md5=320df6df0ac072363926b88dc749a040
Keywords: Estrogen Receptor, Gene Product, Messenger Rna, Progesterone Receptor, Receptor Subtype, Retinoic Acid Receptor, Retinol Binding Protein, Retinol Derivative, Adult, Aged, Article, Breast Carcinoma, Cancer Control, Clinical Article, Controlled Study, Drug Targeting, Fibrocystic Breast Disease, Human, Human Tissue, Priority Journal, Protein Induction, Receptor Upregulation, Reverse Transcription Polymerase Chain Reaction, Breast Neoplasms, Female, Middle Aged, Retinol-Binding Proteins, Genetic,
Affiliations:
Istituto di Endocrinologia, Facoltá di Medicina, Seconda Universitá di Napoli, Naples, Italy
Ist. Naz. Tumori Fondazione G. P., Univ.́ di Napoli Federico II, Naples, Italy
Istituto di Medicina Nucleare, Univ.́ di Napoli Federico II, Naples, Italy
Dipto. Biochim. Biotecnologie M., Univ.́ di Napoli Federico II, Naples, Italy
Cattedra di Endocrinologia, Seconda Universita'di Napoli, via Pansini 5, 80131 Naples, Italy
References:
Not available.
Eur J Endocrinol (ISSN: 0804-4643), 1997 Oct; 137(4): 410-414.
Export to BibTeX Export to EndNote
Paper type: Journal Article,
Impact factor: 1.968, 5-year impact factor: 3.325
Url: http://www.scopus.com/inward/record.url?eid=2-s2.0-0030869575&partnerID=40&md5=320df6df0ac072363926b88dc749a040
Keywords: Estrogen Receptor, Gene Product, Messenger Rna, Progesterone Receptor, Receptor Subtype, Retinoic Acid Receptor, Retinol Binding Protein, Retinol Derivative, Adult, Aged, Article, Breast Carcinoma, Cancer Control, Clinical Article, Controlled Study, Drug Targeting, Fibrocystic Breast Disease, Human, Human Tissue, Priority Journal, Protein Induction, Receptor Upregulation, Reverse Transcription Polymerase Chain Reaction, Breast Neoplasms, Female, Middle Aged, Retinol-Binding Proteins, Genetic,
Affiliations:
Istituto di Endocrinologia, Facoltá di Medicina, Seconda Universitá di Napoli, Naples, Italy
Ist. Naz. Tumori Fondazione G. P., Univ.́ di Napoli Federico II, Naples, Italy
Istituto di Medicina Nucleare, Univ.́ di Napoli Federico II, Naples, Italy
Dipto. Biochim. Biotecnologie M., Univ.́ di Napoli Federico II, Naples, Italy
Cattedra di Endocrinologia, Seconda Universita'di Napoli, via Pansini 5, 80131 Naples, Italy
References:
Not available.
Retinoic acid receptors α, β and γ, and cellular retinol binding protein-I expression in breast fibrocystic disease and cancer
Retinoids seem to act as agents of chemoprevention and differentiation in breast diseases. Their action is mediated by nuclear receptors, retinoic acid receptors (RARα, RARβ, RARγ) and retinoid X receptors (RXRα, RXRβ, RXRγ,) and modulated by cellular retinol binding proteins (CRBP). There are few published data on CRBP expression. In this study, we evaluated the expression of RARα, β and γ and CRBP type I (CRBP-I) gene expression in fibrocystic disease (FD) and in breast cancer (BC), studying 14 FD and 20 BC surgical samples by reverse transcription (RT)-PCR. We also evaluated mRNA concentrations in cancer samples by a semiquantitative PCR method, co- amplifying RARα, RARβ and CRBP-I genes with an unrelated gene, glyceraldehyde 3-phosphate dehydrogenase (GAPDH), as internal control. All benign and malignant breast tissues expressed RARα, β and γ, and CRBP-I mRNAs. A greater concentration of RARβ mRNA was detected in cancer tissues with lower oestrogen and progesterone receptor concentrations, whereas RARe was detected in variable concentrations that were not related to those of steroid receptors. The CRBP-I concentration was similar in all samples studied. We demonstrated that all three PARs and CRBP-I transcripts are expressed in FD, and that RARβ, RARγ and CRBP-I mRNAs also are present in BC tissues. This indicates that both malignant and benign breast tissues may be target for retinoids, justifying the use of natural and synthetic vitamin A derivatives in the chemoprevention of breast disease.
Retinoids seem to act as agents of chemoprevention and differentiation in breast diseases. Their action is mediated by nuclear receptors, retinoic acid receptors (RARα, RARβ, RARγ) and retinoid X receptors (RXRα, RXRβ, RXRγ,) and modulated by cellular retinol binding proteins (CRBP). There are few published data on CRBP expression. In this study, we evaluated the expression of RARα, β and γ and CRBP type I (CRBP-I) gene expression in fibrocystic disease (FD) and in breast cancer (BC), studying 14 FD and 20 BC surgical samples by reverse transcription (RT)-PCR. We also evaluated mRNA concentrations in cancer samples by a semiquantitative PCR method, co- amplifying RARα, RARβ and CRBP-I genes with an unrelated gene, glyceraldehyde 3-phosphate dehydrogenase (GAPDH), as internal control. All benign and malignant breast tissues expressed RARα, β and γ, and CRBP-I mRNAs. A greater concentration of RARβ mRNA was detected in cancer tissues with lower oestrogen and progesterone receptor concentrations, whereas RARe was detected in variable concentrations that were not related to those of steroid receptors. The CRBP-I concentration was similar in all samples studied. We demonstrated that all three PARs and CRBP-I transcripts are expressed in FD, and that RARβ, RARγ and CRBP-I mRNAs also are present in BC tissues. This indicates that both malignant and benign breast tissues may be target for retinoids, justifying the use of natural and synthetic vitamin A derivatives in the chemoprevention of breast disease.
Retinoic acid receptors α, β and γ, and cellular retinol binding protein-I expression in breast fibrocystic disease and cancer
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Retinoic acid receptors α, β and γ, and cellular retinol binding protein-I expression in breast fibrocystic disease and cancer
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Agmon I, Amit M, Auerbach T, Bashan A, Baram D, Bartels H, Berisio R, Greenberg I, Harms J, Hansen HAS, Kessler M, Pyetan E, Schluenzen F, Sittner A, Yonath A, Zarivach R
* Ribosomal crystallography: A flexible nucleotide anchoring tRNA translocation, facilitates peptide-bond formation, chirality discrimination and antibiotics synergism (416 views)
Febs Lett (ISSN: 0014-5793, 0014-5793print, 1873-3468electronic), 2004 Jun 1; 567(1): 20-26.
Impact Factor: 3.843
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Esposito G, Ligresti A, Izzo AA, Bisogno T, Ruvo M, Di Rosa M, Di Marzo V, Iuvone T
* The endocannabinoid system protects rat glioma cells against HIV-1 Tat protein-induced cytotoxicity: Mechanism and regulation (769 views)
Jbc Papers (ISSN: 0021-9258, 1083-351x, 0021-9258linking), 2002 Dec 27; 277(52): 50348-50354.
Impact Factor: 6.696
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Dathan N, Parlato R, Rosica A, De Felice M, Di Lauro R
* Distribution Of The Titf2/Foxe1 Gene Product Is Consistent With An Important Role In The Development Of Foregut Endoderm, Palate, And Hair (301 views)
Developmental Dynamics, 2002; 224: 450-456.
Impact Factor: 2.668
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FRITTITTA L, VIGNERI R, PAPA V, GOLDFINE I, GRASSO G, TRISCHITTA V
Structural and functional studies of insulin receptors in human breast cancer (483 views)
Breast Cancer Res Tr Kluwer Academic Publishers (ISSN: 0167-6806), 1993; 25(1): 73-82.
Impact Factor: 2.43
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Papa V, Reese CC, Brunetti A, Vigneri R, Siiteri PK, Goldfine ID
Progestins increase insulin receptor content and insulin stimulation of growth in human breast carcinoma cells (593 views)
Cancer Res (ISSN: 0008-5472, 1538-7445, 1538-7445electronic), 1990 Dec 15; 50(24): 7858-7862.
Impact Factor: 8.426
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28 Records (27 excluding Abstracts).
Total impact factor: 93.213 (93.213 excluding Abstracts).
Total 5 year impact factor: 92.306 (92.306 excluding Abstracts).
Total impact factor: 93.213 (93.213 excluding Abstracts).
Total 5 year impact factor: 92.306 (92.306 excluding Abstracts).
817 views. Last view on Sunday 13 October 2024, 10:02:44
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