The changes of estrogen receptor-beta variants expression in breast carcinogenesis: Decrease of estrogen receptor-beta2 expression is the key event in breast cancer development
- PMID: 16615154
- DOI: 10.1002/jso.20336
The changes of estrogen receptor-beta variants expression in breast carcinogenesis: Decrease of estrogen receptor-beta2 expression is the key event in breast cancer development
Abstract
Background and objectives: Although more than five variant forms of estrogen receptor-beta (ERbeta) have been identified, their role has not been identified. This study was carried out to investigate the changes of ERbeta variants in breast cancer development.
Methods: Using reverse transcription polymerase chain reaction (RT-PCR) and triple primer PCR (TP-PCR), the expression levels of ERbeta variants mRNA were measured in 66 paired normal and cancer tissues. The relative expression level of ERbeta variants were compared between normal and cancer tissues, and also compared according to various clinicopathological parameters.
Results: Among ERbeta variants, ERbeta2 and ERbeta5 consist of the major proportion of ERbeta expression both in normal and cancer tissues. The ERbeta and ERbeta2 expression levels decreased significantly in the cancers compared with corresponding normal tissues, particularly in ERalpha-expressing cancers. However, ERbeta5 expression level increased significantly in the cancers, especially in those of postmenopausal patients. The relative increase of ERbeta5 expression in cancer tissues was associated with favorable differentiation.
Conclusions: Decrease of ERbeta2 is thought to be the key reason for the decrease in ERbeta expression in cancer tissues, and it is particularly associated with the development of ERalpha-expressing breast cancer.
Copyright 2006 Wiley-Liss, Inc.
Similar articles
-
Distinct mRNA, protein expression patterns and distribution of oestrogen receptors alpha and beta in human primary breast cancer: correlation with proliferation marker Ki-67 and clinicopathological factors.Eur J Cancer. 2005 Dec;41(18):2924-34. doi: 10.1016/j.ejca.2005.09.010. Epub 2005 Nov 10. Eur J Cancer. 2005. PMID: 16289616
-
Expression of estrogen receptor (ER) subtypes and ERbeta isoforms in colon cancer.Cancer Res. 2001 Jan 15;61(2):632-40. Cancer Res. 2001. PMID: 11212261
-
Oestrogen receptors alpha and beta differ in normal human breast and breast carcinomas.J Pathol. 2002 Dec;198(4):450-7. doi: 10.1002/path.1230. J Pathol. 2002. PMID: 12434414
-
Clinical significance of estrogen receptor beta in breast cancer.Cancer Chemother Pharmacol. 2005 Nov;56 Suppl 1:21-6. doi: 10.1007/s00280-005-0107-3. Cancer Chemother Pharmacol. 2005. PMID: 16273360 Review.
-
Estrogen receptor beta in breast cancer--diagnostic and therapeutic implications.Steroids. 2009 Aug;74(8):635-41. doi: 10.1016/j.steroids.2009.02.005. Epub 2009 Mar 4. Steroids. 2009. PMID: 19463683 Review.
Cited by
-
Analysis of estrogen receptor isoforms and variants in breast cancer cell lines.Exp Ther Med. 2011 May;2(3):537-544. doi: 10.3892/etm.2011.226. Epub 2011 Mar 10. Exp Ther Med. 2011. PMID: 22977537 Free PMC article.
-
Estrogen Receptor Beta: The Promising Biomarker and Potential Target in Metastases.Int J Mol Sci. 2021 Feb 6;22(4):1656. doi: 10.3390/ijms22041656. Int J Mol Sci. 2021. PMID: 33562134 Free PMC article. Review.
-
Genes Co-Expressed with ESR2 Influence Clinical Outcomes in Cancer Patients: TCGA Data Analysis.Int J Mol Sci. 2024 Aug 9;25(16):8707. doi: 10.3390/ijms25168707. Int J Mol Sci. 2024. PMID: 39201394 Free PMC article.
-
Divergent mechanisms for trophic actions of estrogens in the brain and peripheral tissues.Brain Res. 2011 Mar 16;1379:119-36. doi: 10.1016/j.brainres.2010.11.081. Epub 2010 Dec 1. Brain Res. 2011. PMID: 21130078 Free PMC article. Review.
-
Estrogen receptor β isoform 5 confers sensitivity of breast cancer cell lines to chemotherapeutic agent-induced apoptosis through interaction with Bcl2L12.Neoplasia. 2013 Nov;15(11):1262-71. doi: 10.1593/neo.131184. Neoplasia. 2013. PMID: 24339738 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical