Expression of prolactin receptor mRNA in oestrogen receptor positive breast cancers pre- and post-tamoxifen therapy

被引:6
|
作者
de Castillo, B
Cawthorn, S
Moppett, J
Shere, M
Norman, M
机构
[1] Univ Bristol, Henry Wellcome Labs Integrat Neurosci & Endocrino, Bristol BS1 3NY, Avon, England
[2] N Bristol NHS Trust, Breast Care Ctr, Bristol BS16 1LE, Avon, England
[3] Univ Bristol, Dept Pathol & Microbiol, Bristol BS8 1TD, Avon, England
来源
EJSO | 2004年 / 30卷 / 05期
关键词
protactin receptor; tamoxifen; breast cancer;
D O I
10.1016/j.ejso.2003.03.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim. Previous in vitro studies have shown that tamoxifen down-regulates protactin receptors in breast cancer cells. The aim of this study was to determine whether similar changes might provide the basis for a predictive test in patients. Methods. Biopsy specimens were obtained from 28 post-menopausal women immediately before initiation of treatment with tamoxifen (20 mg daily) and after treatment for 7 days. Prolactin receptor mRNA, determined by reverse-transcription polymerase chain reaction, was then expressed relative to 18S ribosomal RNA. Results. There was good evidence for a decline in receptor expression in response to treatment with tamoxifen in the whole group (p = 0.036), but with a particularly marked decrease (> 60%) in a sub-group of 11 patients. No clear correlation with tumour type or grade, or with several other markers (progesterone receptor, c-erb B-2, pS2, or Bcl-2) was apparent. Conclusion. Tamoxifen reduces expression of mRNA encoding the protactin receptor in a sub-group of breast tumours and might provide the basis for a predictive test for tamoxifen therapy. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:515 / 519
页数:5
相关论文
共 50 条
  • [41] Whole genome comparisons of pre- and post-aromatase inhibitor treatment in estrogen receptor positive breast cancer
    Ellis, Matthew J.
    Lie, Ding
    Shen, Dong
    Luo, Jingqin
    Suman, Vera J.
    Wallis, John W.
    Van Tine, Brian A.
    Hoog, Jeremy
    Crowder, Robert J.
    Snider, Jacqueline E.
    Ballman, Karla
    Chen, Ken
    Koboldt, Daniel C.
    Schierding, William S.
    McMichael, Joshua F.
    Miller, Christopher A.
    Kandoth, Cyriac
    Lu, Charles
    Harris, Christopher C.
    McLellan, Michael D.
    Wendl, Michael C.
    DeSchryver, Katherine
    Allred, D. Craig
    Esserman, Laura
    Unzeitig, Gary
    Margenthaler, Julie
    Babiera, G. V.
    Marcom, P. Kelly
    Guenther, J. M.
    Leitch, Marilyn
    Hunt, Kelly
    Olson, John
    Tao, Yu
    Fulton, Lucinda L.
    Fulton, Robert S.
    Harrison, Michelle
    Oberkfell, Ben
    Du, Feiyu
    Demeter, Ryan
    Griffith, Malachi
    Vickery, Tammi L.
    McDonald, Sandra A.
    Watson, Mark
    Dooling, David J.
    Ota, David
    Chang, Li-Wei
    Bose, Ron
    Ley, Timothy J.
    Wilson, Richard K.
    Mardis, Elaine R.
    CANCER RESEARCH, 2012, 72
  • [42] Clinicopathological characteristics of oestrogen receptor negative, progesterone receptor positive breast cancers: re-evaluating subsets within this group
    Ahmed, Syed Salahuddin
    Thike, Aye Aye
    Zhang, Kathryn
    Lim, Jeffrey Chun Tatt
    Puay Hoon Tan
    JOURNAL OF CLINICAL PATHOLOGY, 2017, 70 (04) : 320 - 326
  • [43] Androgen Receptor Expression Is a Significant Prognostic Factor in Estrogen Receptor Positive Breast Cancers Treated with Chemo-Endocrine Therapy
    Castellano, I.
    Allia, E.
    Accortanzo, V.
    Vandone, A. M.
    Chiusa, L.
    Arisio, R.
    Durando, A.
    Donadio, M.
    Bussolati, G.
    Coates, A. S.
    Viale, G.
    Sapino, A.
    LABORATORY INVESTIGATION, 2010, 90 : 39A - 39A
  • [44] Androgen Receptor Expression Is a Significant Prognostic Factor in Estrogen Receptor Positive Breast Cancers Treated with Chemo-Endocrine Therapy
    Castellano, I.
    Allia, E.
    Accortanzo, V.
    Vandone, A. M.
    Chiusa, L.
    Arisio, R.
    Durando, A.
    Donadio, M.
    Bussolati, G.
    Coates, A. S.
    Viale, G.
    Sapino, A.
    MODERN PATHOLOGY, 2010, 23 : 39A - 39A
  • [45] Relationship of coregulator and oestrogen receptor isoform expression to de novo tamoxifen resistance in human breast cancer
    Murphy, LC
    Leygue, E
    Niu, Y
    Snell, L
    Ho, SM
    Watson, PH
    BRITISH JOURNAL OF CANCER, 2002, 87 (12) : 1411 - 1416
  • [46] Relationship of coregulator and oestrogen receptor isoform expression to de novo tamoxifen resistance in human breast cancer
    L C Murphy
    E Leygue
    Y Niu
    L Snell
    S-M Ho
    P H Watson
    British Journal of Cancer, 2002, 87 : 1411 - 1416
  • [47] Increased expression of estrogen receptor β mRNA in tamoxifen-resistant breast cancer patients
    Speirs, V
    Malone, C
    Walton, DS
    Kerin, MJ
    Atkin, SL
    CANCER RESEARCH, 1999, 59 (21) : 5421 - 5424
  • [48] Age specific variation of oestrogen and progesterone receptor expression in 1340 primary operable breast cancers
    Neven, P.
    Huang, H. J.
    Drijkoningen, M.
    Armant, F.
    Berteloot, P.
    Van Limbergen, E.
    Thomas, J.
    Paridaens, R.
    Vergote, I.
    Christiaens, M.
    EJC SUPPLEMENTS, 2004, 2 (03): : 177 - 178
  • [49] Mammographic density changes following discontinuation of tamoxifen in premenopausal women with oestrogen receptor-positive breast cancer
    Won Hwa Kim
    Nariya Cho
    Young-Seon Kim
    Ann Yi
    European Radiology, 2018, 28 : 3176 - 3184
  • [50] 17β-Hydroxysteroid Dehydrogenase Type 14 Is a Predictive Marker for Tamoxifen Response in Oestrogen Receptor Positive Breast Cancer
    Sivik, Tove
    Gunnarsson, Cecilia
    Fornander, Tommy
    Nordenskjold, Bo
    Skoog, Lambert
    Stal, Olle
    Jansson, Agneta
    PLOS ONE, 2012, 7 (07):