Prognostic value of cyclin E expression in breast cancer: a meta-analysis

被引:24
作者
Gao, Sheng [1 ]
Ma, Jing-Jing [1 ]
Lu, Cheng [1 ]
机构
[1] Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Dept Breast Surg, State Key Lab Reprod Med, Nanjing 210004, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Cyclin E; Breast cancer; Prognosis; Disease-free survival; Meta-analysis; E OVEREXPRESSION; POOR SURVIVAL; MARKER; PREMENOPAUSAL; P27(KIP1); PHENOTYPE; THERAPY; COMPLEX; RELAPSE; PROTEIN;
D O I
10.1007/s13277-013-0915-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cyclin E is an important regulator of cell cycle progression. Various studies examined the relationship between cyclin E overexpression with the clinical outcome in patients with breast cancer but yielded conflicting results. Electronic databases updated to May 2013 were searched to find relevant studies. A meta-analysis was conducted with eligible studies which quantitatively evaluated the relationship between cyclin E overexpression and survival of patients with breast cancer. Survival data were aggregated and quantitatively analyzed. We conducted a final analysis of 7,759 patients from 23 eligible studies and evaluated the correlation between cyclin E overexpression and survival in patients with breast cancer. Combined hazard ratios suggested that cyclin E overexpression had an unfavorable impact on overall survival (OS) (hazard ratio (HR) = 1.30, 95 % confidence interval (CI), 1.12-1.49) and breast cancer-specific survival (BCSS) (HR = 1.48, 95 % CI, 1.03-1.93), but not disease-free survival (HR = 1.11; 95 % CI, 0.96-1.27) in patients with breast cancer. Significantly, risks were found among stage I-II breast cancer for (HR = 1.75; 95 % CI, 1.30-2.19). Cyclin E overexpression is associated with poor OS and BCSS in breast cancer.
引用
收藏
页码:3423 / 3430
页数:8
相关论文
共 49 条
[1]   Systematic reviews in health care - Systematic reviews of evaluations of prognostic variables [J].
Altman, DG .
BMJ-BRITISH MEDICAL JOURNAL, 2001, 323 (7306) :224-228
[2]   Placental cadherin and the basal epithelial phenotype of BRCA1-related breast cancer [J].
Arnes, JB ;
Brunet, JS ;
Stefansson, I ;
Bégin, LR ;
Wong, N ;
Chappuis, PO ;
Akslen, LA ;
Foulkes, WD .
CLINICAL CANCER RESEARCH, 2005, 11 (11) :4003-4011
[3]   OPERATING CHARACTERISTICS OF A BANK CORRELATION TEST FOR PUBLICATION BIAS [J].
BEGG, CB ;
MAZUMDAR, M .
BIOMETRICS, 1994, 50 (04) :1088-1101
[4]   PUBLICATION BIAS - A PROBLEM IN INTERPRETING MEDICAL DATA [J].
BEGG, CB ;
BERLIN, JA .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES A-STATISTICS IN SOCIETY, 1988, 151 :419-463
[5]   Cyclin e overexpression reduces infiltrative growth in breast cancer - Yet another link between proliferation control and tumor invasion [J].
Berglund, Pontus ;
Landberg, Goran .
CELL CYCLE, 2006, 5 (06) :606-609
[6]   Induction of mammary gland hyperplasia and carcinomas in transgenic mice expressing human cyclin E [J].
Bortner, DM ;
Rosenberg, MP .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (01) :453-459
[7]   CA IX is an independent prognostic marker in premenopausal breast cancer patients with one to three positive lymph nodes and a putative marker of radiation resistance [J].
Brennan, Donal J. ;
Jirstrom, Karin ;
Kronblad, Asa ;
Millikan, Robert C. ;
Landberg, Goran ;
Duffy, Michael J. ;
Ryden, Lisa ;
Gallagher, William M. ;
O'Brien, Sallyann L. .
CLINICAL CANCER RESEARCH, 2006, 12 (21) :6421-6431
[8]   Over-expression of cyclin A is highly associated with early relapse and reduced survival in patients with primary breast carcinomas [J].
Bukholm, IRK ;
Bukholm, G ;
Nesland, JM .
INTERNATIONAL JOURNAL OF CANCER, 2001, 93 (02) :283-287
[9]   Bcl-2 is a prognostic marker in breast cancer independently of the Nottingham Prognostic Index [J].
Callagy, GM ;
Pharoah, PD ;
Pinder, SE ;
Hsu, FD ;
Nielsen, TO ;
Ragaz, J ;
Ellis, IO ;
Huntsman, D ;
Caldas, C .
CLINICAL CANCER RESEARCH, 2006, 12 (08) :2468-2475
[10]   Meta-analysis confirms BCL2 is an independent prognostic marker in breast cancer [J].
Callagy, Grace M. ;
Webber, Mark J. ;
Pharoah, Paul D. P. ;
Caldas, Carlos .
BMC CANCER, 2008, 8 (1)