Increased Expression of Follistatin in Breast Cancer Reduces Invasiveness and Clinically Correlates with Better Survival

被引:19
作者
Zabkiewicz, Catherine [1 ]
Resaul, Jeyna [1 ]
Hargest, Rachel [1 ]
Jiang, Wen Guo [1 ]
Ye, Lin [1 ]
机构
[1] Cardiff Univ, Sch Med, Cardiff China Med Res Collaborat, Henry Wellcome Bldg, Cardiff CF14 4XN, S Glam, Wales
关键词
Follistatin; breast cancer; survival; ACTIVIN-A; BONE METASTASIS; CELL; GROWTH; TRANSCRIPTION; FLRG; ANTAGONISTS; MECHANISMS; CARCINOMA; PROTEINS;
D O I
10.21873/cgp.20035
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: Activin and its antagonist follistatin (FST) have been implicated in several solid tumours. This study investigated the role of FST in breast cancer. Materials and Methods: FST expression was examined using reverse transcription polymerase chain reaction (RT-PCR), real-time quantitative polymerase chain reaction (qPCR) and immunohistochemistry in a cohort of breast cancer samples. Expression was correlated to pathological and prognostic parameters in our patient cohort. FST was overexpressed in MCF-7 cells and assays for growth and invasion were performed. Results: FST is expressed in breast tissue, in the cytoplasm of mammary epithelial cells. Expression was decreased in breast cancer tissue in comparison to normal mammary tissue. Over-expression of FST in vitro led to significantly increased growth rate and reduced invasion. Higher FST associates with lower-grade tumours and better survival. Conclusion: Our results suggest a role for FST as a suppressor of invasion and metastasis in breast cancer.
引用
收藏
页码:241 / 251
页数:11
相关论文
共 34 条
[1]   The bright and the dark sides of activin in wound healing and cancer [J].
Antsiferova, Maria ;
Werner, Sabine .
JOURNAL OF CELL SCIENCE, 2012, 125 (17) :3929-3937
[2]   Transcription activation of FLRG and follistatin by activin A, through Smad proteins, participates in a negative feedback loop to modulate activin A function [J].
Bartholin, L ;
Maguer-Satta, V ;
Hayette, S ;
Martel, S ;
Badoux, M ;
Corbo, L ;
Magaud, JP ;
Rimokh, R .
ONCOGENE, 2002, 21 (14) :2227-2235
[3]   Activin-a signaling promotes epithelial–mesenchymal transition, invasion, and metastatic growth of breast cancer [J].
Bashir M. ;
Damineni S. ;
Mukherjee G. ;
Kondaiah P. .
npj Breast Cancer, 1 (1)
[4]   Differential expression of follistatin and FLRG in human breast proliferative disorders [J].
Bloise, Enrrico ;
Couto, Henrique L. ;
Massai, Lauretta ;
Ciarmela, Pasquapina ;
Mencarelli, Marzia ;
Borges, Lavinia E. ;
Muscettola, Michela ;
Grasso, Giovanni ;
Amaral, Vania F. ;
Cassali, Geovanni D. ;
Petraglia, Felice ;
Reis, Fernando M. .
BMC CANCER, 2009, 9 :320
[5]   Activin A mediates growth inhibition and cell cycle arrest through smads in human breast cancer cells [J].
Burdette, JE ;
Jeruss, JS ;
Kurley, SJ ;
Lee, EJ ;
Woodruff, TK .
CANCER RESEARCH, 2005, 65 (17) :7968-7975
[6]   Activin and estrogen crosstalk regulates transcription in human breast cancer cells [J].
Burdette, Joanna E. ;
Woodruff, Teresa K. .
ENDOCRINE-RELATED CANCER, 2007, 14 (03) :679-689
[7]  
Couto HL, 2016, APPL IMMUNOHISTOCHEM
[8]   Mechanisms of action of bone morphogenetic proteins in cancer [J].
Davis, Hayley ;
Raja, Erna ;
Miyazono, Kohei ;
Tsubakihara, Yutaro ;
Moustakas, Aristidis .
CYTOKINE & GROWTH FACTOR REVIEWS, 2016, 27 :81-92
[9]   Activins and activin antagonists in hepatocellular carcinoma [J].
Deli, Alev ;
Kreidl, Emanuel ;
Santifaller, Stefan ;
Trotter, Barbara ;
Seir, Katja ;
Berger, Walter ;
Schulte-Hermann, Rolf ;
Rodgarkia-Dara, Chantal ;
Grusch, Michael .
WORLD JOURNAL OF GASTROENTEROLOGY, 2008, 14 (11) :1699-1709
[10]   Antagonists of activin signaling: mechanisms and potential biological applications [J].
Harrison, CA ;
Gray, PC ;
Vale, WW ;
Robertson, DM .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2005, 16 (02) :73-78