JCP

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS REGISTER
[Advanced]

Journal of Clinical Pathology 2008;61:197-203; doi:10.1136/jcp.2006.040378
Copyright © 2008 by the BMJ Publishing Group Ltd & Association of Clinical Pathologists.

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Read responses to this article
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this link to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Add article to my folders
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Borgquist, S
Right arrow Articles by Jirström, K
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Borgquist, S
Right arrow Articles by Jirström, K
Right arrowPubmed/NCBI databases
Medline Plus Health Information
*Breast Cancer

ORIGINAL ARTICLES

Oestrogen receptors {alpha} and β show different associations to clinicopathological parameters and their co-expression might predict a better response to endocrine treatment in breast cancer

S Borgquist1,2, C Holm1, M Stendahl1, L Anagnostaki1, G Landberg1, K Jirström1

1 Division of Pathology, Department of Laboratory Medicine; Malmö University Hospital, Malmö, Sweden
2 Division of Oncology, Department of Clinical Sciences, Lund University Hospital, Lund, Sweden

Correspondence to:
Karin Jirström, Division of Pathology, Department of Laboratory Medicine, Lund University, Malmö University Hospital, S-205 02 Malmö, Sweden; karin.jirstrom{at}med.lu.se

Aims: The majority of all breast cancers are hormone responsive, traditionally defined by the expression of oestrogen receptor (ER) {alpha} and/or progesterone receptors. In contrast to ER{alpha}, the clinical significance of the relatively recently identified ERβ is still unclear. This study aimed to define the relationship between ERβ and clinicopathological parameters in a mixed cohort of breast cancer and, furthermore, to investigate the impact of ERβ expression on disease outcome.

Methods: The immunohistochemical expression of ER{alpha} and ERβ was analysed in tissue microarrays containing a total number of 512 tumours with all incident breast cancers diagnosed at the Malmö University Hospital between 1988 and 1992.

Results: 78% of the tumours were ER{alpha} positive and 50% were ERβ positive. ERβ correlated positively with ER{alpha} (p = 0.001). In contrast to ER{alpha}, ERβ was not associated with any important clinicopathological variables. Furthermore, no overall prognostic significance could be demonstrated for ERβ. In the ER{alpha}-positive subgroup, however, a low expression of ERβ correlated with a decreased disease-free survival in patients receiving endocrine treatment (p = 0.003).

Conclusions: Although interrelated, ER{alpha} and ERβ seem to be differentially associated to clinicopathological parameters, and this would support the fact that they might have different functions in vivo. Furthermore, ERβ might be a predictive marker of response to endocrine therapy, although this needs to be confirmed in additional studies, preferably randomised trials.





This article has been cited by other articles:


Home page
J. Clin. Pathol.Home page
V Speirs, C A Green, and A M Shaaban
Oestrogen receptor {beta} immunohistochemistry: time to get it right?
J. Clin. Pathol., October 1, 2008; 61(10): 1150 - 1151.
[Full Text] [PDF]

eLetters:

Read all eLetters

Estrogen receptor beta immunohistochemistry: time to get it right
Valerie Speirs, et al.
JCP Online, 31 Mar 2008 [Full text]



HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS REGISTER
Journal of Clinical Pathology Molecular Pathology
Terms and conditions relating to subscriptions purchased online  ¦  Website terms and conditions  ¦  Privacy policy
Copyright © 2008 by the BMJ Publishing Group Ltd & Association of Clinical Pathologists.