File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1002/path.6157
- Scopus: eid_2-s2.0-85166941471
- WOS: WOS:001043412400001
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Overexpression of BQ323636.1 contributes to anastrozole resistance in AR+ve/ER+ve breast cancer
Title | Overexpression of BQ323636.1 contributes to anastrozole resistance in AR+ve/ER+ve breast cancer |
---|---|
Authors | |
Keywords | anastrozole androgen receptor AR antagonist aromatase inhibitor resistance BQ323636.1 breast cancer oestrogen receptor |
Issue Date | 9-Aug-2023 |
Publisher | Pathological Society of Great Britain and Ireland |
Citation | Journal of Pathology, 2023, v. 260, n. 4, p. 156-168 How to Cite? |
Abstract | Aromatase inhibitors (Ais) are used as adjuvant endocrine therapy for oestrogen receptor-positive (ER+ve) post-menopausal breast cancer patients. Ais, by inhibiting the enzyme aromatase, block the conversion of androgen to oestrogen, reducing oestrogen levels. Resistance to Ais limits their clinical utilisation. Here, we show that overexpression of BQ323636.1 (BQ), a novel splice variant of nuclear co-repressor NCOR2, is associated with resistance to the non-steroidal aromatase inhibitor anastrozole in ER+ve post-menopausal breast cancer. Mechanistic study indicates that BQ overexpression enhances androgen receptor (AR) activity and in the presence of anastrozole, causes hyper-activation of AR signalling, which unexpectedly enhanced cell proliferation, through increased expression of CDK2, CDK4, and CCNE1. BQ overexpression reverses the effect of anastrozole in ER+ve breast cancer in an AR-dependent manner, whilst co-treatment with the AR antagonist bicalutamide recovered its therapeutic effect both in vitro and in vivo. Thus, for BQ-overexpressing breast cancer, targeting AR can combat anastrozole resistance. Clinical study of 268 primary breast cancer samples of ER+ve patients who had been treated with non-steroidal Ais showed 32.5% (38/117) of cases with combined high nuclear expression of BQ and AR, which were found to be significantly associated with Ai resistance. Non-steroidal Ai-treated patients with high nuclear expression of both BQ and AR had poorer overall, disease-specific, and disease-free survival. These findings suggest the importance of assessing BQ and AR expression status in the primary ER+ve breast tumour prior to Ai treatment. This may save patients from inappropriate treatment and enable effective therapy to be given at an early stage. © 2023 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland. |
Persistent Identifier | http://hdl.handle.net/10722/331396 |
ISSN | 2023 Impact Factor: 5.6 2023 SCImago Journal Rankings: 2.426 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Tsoi, H | - |
dc.contributor.author | Lok, J | - |
dc.contributor.author | Man, EP | - |
dc.contributor.author | Cheng, CN | - |
dc.contributor.author | Leung, MH | - |
dc.contributor.author | You, CP | - |
dc.contributor.author | Chan, SY | - |
dc.contributor.author | Chan, WL | - |
dc.contributor.author | Khoo, US | - |
dc.date.accessioned | 2023-09-21T06:55:20Z | - |
dc.date.available | 2023-09-21T06:55:20Z | - |
dc.date.issued | 2023-08-09 | - |
dc.identifier.citation | Journal of Pathology, 2023, v. 260, n. 4, p. 156-168 | - |
dc.identifier.issn | 0022-3417 | - |
dc.identifier.uri | http://hdl.handle.net/10722/331396 | - |
dc.description.abstract | <p>Aromatase inhibitors (Ais) are used as adjuvant endocrine therapy for oestrogen receptor-positive (ER+ve) post-menopausal breast cancer patients. Ais, by inhibiting the enzyme aromatase, block the conversion of androgen to oestrogen, reducing oestrogen levels. Resistance to Ais limits their clinical utilisation. Here, we show that overexpression of BQ323636.1 (BQ), a novel splice variant of nuclear co-repressor NCOR2, is associated with resistance to the non-steroidal aromatase inhibitor anastrozole in ER+ve post-menopausal breast cancer. Mechanistic study indicates that BQ overexpression enhances androgen receptor (AR) activity and in the presence of anastrozole, causes hyper-activation of AR signalling, which unexpectedly enhanced cell proliferation, through increased expression of <em>CDK2</em>, <em>CDK4</em>, and <em>CCNE1</em>. BQ overexpression reverses the effect of anastrozole in ER+ve breast cancer in an AR-dependent manner, whilst co-treatment with the AR antagonist bicalutamide recovered its therapeutic effect both <em>in vitro</em> and <em>in vivo</em>. Thus, for BQ-overexpressing breast cancer, targeting AR can combat anastrozole resistance. Clinical study of 268 primary breast cancer samples of ER+ve patients who had been treated with non-steroidal Ais showed 32.5% (38/117) of cases with combined high nuclear expression of BQ and AR, which were found to be significantly associated with Ai resistance. Non-steroidal Ai-treated patients with high nuclear expression of both BQ and AR had poorer overall, disease-specific, and disease-free survival. These findings suggest the importance of assessing BQ and AR expression status in the primary ER+ve breast tumour prior to Ai treatment. This may save patients from inappropriate treatment and enable effective therapy to be given at an early stage. © 2023 The Authors. <em>The Journal of Pathology</em> published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.</p> | - |
dc.language | eng | - |
dc.publisher | Pathological Society of Great Britain and Ireland | - |
dc.relation.ispartof | Journal of Pathology | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | anastrozole | - |
dc.subject | androgen receptor | - |
dc.subject | AR antagonist | - |
dc.subject | aromatase inhibitor resistance | - |
dc.subject | BQ323636.1 | - |
dc.subject | breast cancer | - |
dc.subject | oestrogen receptor | - |
dc.title | Overexpression of BQ323636.1 contributes to anastrozole resistance in AR+ve/ER+ve breast cancer | - |
dc.type | Article | - |
dc.identifier.doi | 10.1002/path.6157 | - |
dc.identifier.scopus | eid_2-s2.0-85166941471 | - |
dc.identifier.volume | 260 | - |
dc.identifier.issue | 4 | - |
dc.identifier.spage | 156 | - |
dc.identifier.epage | 168 | - |
dc.identifier.eissn | 1096-9896 | - |
dc.identifier.isi | WOS:001043412400001 | - |
dc.identifier.issnl | 0022-3417 | - |