GATA3 mRNA expression, but not mutation, associates with longer progression-free survival in ER-positive breast cancer patients treated with first-line tamoxifen for recurrent disease

被引:24
作者
Liu, Jingjing [1 ]
Prager-van der Smissen, Wendy J. C. [1 ]
Look, Maxime P. [1 ]
Sieuwerts, Anieta M. [1 ,2 ]
Smid, Marcel [1 ]
Meijer-van Gelder, Marion E. [1 ]
Foekens, John A. [1 ]
Hollestelle, Antoinette [1 ]
Martens, John W. M. [1 ]
机构
[1] Erasmus MC Canc Inst, Dept Med Oncol, Wytemaweg 80, NL-3015 CN Rotterdam, Netherlands
[2] Canc Genom Netherlands, Amsterdam, Netherlands
关键词
Tamoxifen; GATA3; Mutation; Expression; Recurrent breast cancer; ESTROGEN-RECEPTOR; PROGNOSTIC VALUE; MAMMARY-GLAND; TUMORS; GENE; DIFFERENTIATION; THERAPY; IDENTIFICATION; MORPHOGENESIS; CHEMOTHERAPY;
D O I
10.1016/j.canlet.2016.03.038
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In breast cancer, GATA3 mutations have been associated with a favorable prognosis and the response to neoadjuvant aromatase inhibitor treatment. Therefore, we investigated whether GATA3 mutations predict the outcome of tamoxifen treatment in the advanced setting. In a retrospective study consisting of 235 hormone-naive patients with ER-positive breast cancer who received tamoxifen as first-line treatment for recurrent disease, GATA3 mutations (in 14.0% of patients) did not significantly associate with either the overall response rate (ORR) or with the length of progression-free survival (PFS) after the start of tamoxifen therapy. Interestingly, among 148 patients for whom both mutation and mRNA expression data were available, GATA3 mutations associated with an increased expression of GATA3. However, only 23.7% of GATA3 high tumors had a mutation. Evaluation of the clinical significance of GATA3 mRNA revealed that it was associated with prolonged PFS, but not with the ORR, also in multivariate analysis. Thus, GATA3 mRNA expression, but not GATA3 mutation, is an independent predictor of prolonged PFS in ER-positive breast cancer patients who received first-line tamoxifen for recurrent disease. Besides GATA3 mutation, other mechanisms must exist that underlie increased GATA3 levels. (C) 2016 The Authors. Published by Elsevier Ireland Ltd.
引用
收藏
页码:104 / 109
页数:6
相关论文
共 44 条
[1]   Expression of FOXA1 and GATA-3 in breast cancer: the prognostic significance in hormone receptor-negative tumours [J].
Albergaria, Andre ;
Paredes, Joana ;
Sousa, Barbara ;
Milanezi, Fernanda ;
Carneiro, Vitor ;
Bastos, Joana ;
Costa, Sandra ;
Vieira, Daniella ;
Lopes, Nair ;
Lam, Eric W. ;
Lunet, Nuno ;
Schmitt, Fernando .
BREAST CANCER RESEARCH, 2009, 11 (03)
[2]   Gata-3 is an essential regulator of mammary-gland morphogenesis and luminal-cell differentiation [J].
Asselin-Labat, Marie-Liesse ;
Sutherland, Kate D. ;
Barker, Holly ;
Thomas, Richard ;
Shackleton, Mark ;
Forrest, Natasha C. ;
Hartley, Lynne ;
Robb, Lorraine ;
Grosveld, Frank G. ;
van der Wees, Jacqueline ;
Lindeman, Geoffrey J. ;
Visvader, Jane E. .
NATURE CELL BIOLOGY, 2007, 9 (02) :201-U103
[3]   Sequence analysis of mutations and translocations across breast cancer subtypes [J].
Banerji, Shantanu ;
Cibulskis, Kristian ;
Rangel-Escareno, Claudia ;
Brown, Kristin K. ;
Carter, Scott L. ;
Frederick, Abbie M. ;
Lawrence, Michael S. ;
Sivachenko, Andrey Y. ;
Sougnez, Carrie ;
Zou, Lihua ;
Cortes, Maria L. ;
Fernandez-Lopez, Juan C. ;
Peng, Shouyong ;
Ardlie, Kristin G. ;
Auclair, Daniel ;
Bautista-Pina, Veronica ;
Duke, Fujiko ;
Francis, Joshua ;
Jung, Joonil ;
Maffuz-Aziz, Antonio ;
Onofrio, Robert C. ;
Parkin, Melissa ;
Pho, Nam H. ;
Quintanar-Jurado, Valeria ;
Ramos, Alex H. ;
Rebollar-Vega, Rosa ;
Rodriguez-Cuevas, Sergio ;
Romero-Cordoba, Sandra L. ;
Schumacher, Steven E. ;
Stransky, Nicolas ;
Thompson, Kristin M. ;
Uribe-Figueroa, Laura ;
Baselga, Jose ;
Beroukhim, Rameen ;
Polyak, Kornelia ;
Sgroi, Dennis C. ;
Richardson, Andrea L. ;
Jimenez-Sanchez, Gerardo ;
Lander, Eric S. ;
Gabriel, Stacey B. ;
Garraway, Levi A. ;
Golub, Todd R. ;
Melendez-Zajgla, Jorge ;
Toker, Alex ;
Getz, Gad ;
Hidalgo-Miranda, Alfredo ;
Meyerson, Matthew .
NATURE, 2012, 486 (7403) :405-409
[4]   Tumor aromatase expression as a prognostic factor for local control in young breast cancer patients after breast-conserving treatment [J].
Bollet, Marc A. ;
Savignoni, Alexia ;
De Koning, Leanne ;
Tran-Perennou, Carine ;
Barbaroux, Catherine ;
Degeorges, Armelle ;
Sigal-Zafrani, Brigitte ;
Almouzni, Genevieve ;
Cottu, Paul ;
Salmon, Remy ;
Servant, Nicolas ;
Fourquet, Alain ;
de Cremoux, Patricia .
BREAST CANCER RESEARCH, 2009, 11 (04)
[5]   The significance of GATA3 expression in breast cancer: a 10-year follow-up study [J].
Ciocca, Vincenzo ;
Daskalakis, Constantine ;
Ciocca, Robin M. ;
Ruiz-Orrico, Alejandra ;
Palazzo, Juan P. .
HUMAN PATHOLOGY, 2009, 40 (04) :489-495
[6]   Endocrine resistance in breast cancer - An overview and update [J].
Clarke, Robert ;
Tyson, John J. ;
Dixon, J. Michael .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2015, 418 :220-234
[7]  
den Dunnen JT, 2000, HUM MUTAT, V15, P7
[8]   Whole-genome analysis informs breast cancer response to aromatase inhibition [J].
Ellis, Matthew J. ;
Ding, Li ;
Shen, Dong ;
Luo, Jingqin ;
Suman, Vera J. ;
Wallis, John W. ;
Van Tine, Brian A. ;
Hoog, Jeremy ;
Goiffon, Reece J. ;
Goldstein, Theodore C. ;
Ng, Sam ;
Lin, Li ;
Crowder, Robert ;
Snider, Jacqueline ;
Ballman, Karla ;
Weber, Jason ;
Chen, Ken ;
Koboldt, Daniel C. ;
Kandoth, Cyriac ;
Schierding, William S. ;
McMichael, Joshua F. ;
Miller, Christopher A. ;
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 ;
Maher, Christopher A. ;
Fulton, Lucinda L. ;
Fulton, Robert S. ;
Harrison, Michelle ;
Oberkfell, Ben ;
Du, Feiyu ;
Demeter, Ryan ;
Vickery, Tammi L. ;
Elhammali, Adnan ;
Piwnica-Worms, Helen ;
McDonald, Sandra ;
Watson, Mark .
NATURE, 2012, 486 (7403) :353-360
[9]  
European Organization for Research and Treatment of Cancer BCCG, 2000, MAN CLIN RES TREATM, P116
[10]  
FOEKENS JA, 1989, CANCER RES, V49, P5823