» Articles » PMID: 10705921

Role of Retinoid Receptors in the Prevention and Treatment of Breast Cancer

Overview
Date 2000 Mar 8
PMID 10705921
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Retinoids are vitamin A-related compounds that have been found to prevent cancer in animals and humans. In this review, we discuss the role of retinoids and their receptors in the treatment and prevention of breast cancer. The retinoid receptors are expressed in normal and malignant breast cells, and are critical for normal development. In breast cells, when bound by retinoid hormones, these proteins regulate proliferation, apoptosis, and differentiation. The mechanism by which retinoids inhibit breast cell growth has not been completely elucidated, however, retinoids have been shown to affect multiple signal transduction pathways, including IGF-, TGFbeta-, and AP-1-dependent pathways. Retinoids have also been shown to suppress the growth and prevent the development of breast cancer in animals. These agents suppress tumorigenesis in carcinogen-treated rats and in transgenic mice, and inhibit the growth of transplanted breast tumors. These promising preclinical results have provided the rationale to test retinoids in clinical trials for the treatment and prevention of breast cancer. Several retinoids, including all trans retinoic acid and 9-cis retinoic acid, have been shown to have modest activity in the treatment of breast cancer, and these agents are now in clinical trials in combination with cytotoxic agents and anti-estrogens. Another retinoid, 4-HPR, is currently being tested in a human cancer prevention trial. Preliminary results suggest that 4-HPR may suppress breast cancer development in premenopausal women. Future clinical trials will focus on testing new synthetic retinoids that have reduced toxicity and enhanced therapeutic and preventive efficacy.

Citing Articles

Translation of a Tissue-Selective Rexinoid, UAB30, to the Clinic for Breast Cancer Prevention.

Muccio D, Atigadda V, Brouillette W, Bland K, Krontiras H, Grubbs C Curr Top Med Chem. 2016; 17(6):676-695.

PMID: 27320329 PMC: 9904082. DOI: 10.2174/1568026616666160617093604.


During hormone depletion or tamoxifen treatment of breast cancer cells the estrogen receptor apoprotein supports cell cycling through the retinoic acid receptor α1 apoprotein.

Salazar M, Ratnam M, Patki M, Kisovic I, Trumbly R, Iman M Breast Cancer Res. 2011; 13(1):R18.

PMID: 21299862 PMC: 3109587. DOI: 10.1186/bcr2827.


The rexinoid bexarotene represses cyclin D1 transcription by inducing the DEC2 transcriptional repressor.

Li Y, Shen Q, Kim H, Bissonnette R, Lamph W, Yan B Breast Cancer Res Treat. 2010; 128(3):667-77.

PMID: 20821348 PMC: 3444826. DOI: 10.1007/s10549-010-1083-9.


Retinoid-induced histone deacetylation inhibits telomerase activity in estrogen receptor-negative breast cancer cells.

Phipps S, Love W, White T, Andrews L, Tollefsbol T Anticancer Res. 2010; 29(12):4959-64.

PMID: 20044602 PMC: 2888005.


Expression analyses of nuclear receptor genes in breast cancer cell lines exposed to soy phytoestrogens after BRCA2 knockdown by TaqMan Low-Density Array (TLDA).

Satih S, Savinel H, Rabiau N, Fontana L, Bignon Y, Bernard-Gallon D J Mol Signal. 2009; 4:3.

PMID: 19442290 PMC: 2687443. DOI: 10.1186/1750-2187-4-3.


References
1.
Veronesi U, De Palo G, Costa A, Formelli F, Marubini E, Del Vecchio M . Chemoprevention of breast cancer with retinoids. J Natl Cancer Inst Monogr. 1992; (12):93-7. View

2.
Anzano M, Peer C, Smith J, Mullen L, Shrader M, Logsdon D . Chemoprevention of mammary carcinogenesis in the rat: combined use of raloxifene and 9-cis-retinoic acid. J Natl Cancer Inst. 1996; 88(2):123-5. DOI: 10.1093/jnci/88.2.123. View

3.
Lee J, Newman R, Lippman S, Huber M, Minor T, Raber M . Phase I evaluation of all-trans-retinoic acid in adults with solid tumors. J Clin Oncol. 1993; 11(5):959-66. DOI: 10.1200/JCO.1993.11.5.959. View

4.
Bischoff E, Gottardis M, MOON T, HEYMAN R, Lamph W . Beyond tamoxifen: the retinoid X receptor-selective ligand LGD1069 (TARGRETIN) causes complete regression of mammary carcinoma. Cancer Res. 1998; 58(3):479-84. View

5.
Hong W, Lippman S, Itri L, Karp D, Lee J, Byers R . Prevention of second primary tumors with isotretinoin in squamous-cell carcinoma of the head and neck. N Engl J Med. 1990; 323(12):795-801. DOI: 10.1056/NEJM199009203231205. View