Expression of bone morphogenetic protein-2 and its receptors in epithelial ovarian cancer and their influence on the prognosis of ovarian cancer patients

被引:75
作者
Ma, Ying [1 ]
Ma, Lin [1 ]
Guo, Quan [1 ]
Zhang, Shulan [1 ]
机构
[1] China Med Univ, Shengjing Hosp, Dept Obstet & Gynecol, Shenyang 110004, Peoples R China
关键词
RETINOBLASTOMA PROTEIN; GENE-EXPRESSION; LUNG CARCINOMAS; TUMOR-GROWTH; A549; CELLS; PROLIFERATION; REGULATORS; BMP2;
D O I
10.1186/1756-9966-29-85
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: To determine the expression of bone morphogenetic protein-2 (BMP-2) and its receptors BMPRIA, BMPRIB, and BMPRII in epithelial ovarian cancer (EOC) and to analyze their influence on the prognosis of ovarian cancer patients. Methods: Semi-quantitative RT-PCR and western blot were applied to detect the expression of BMP-2 and its receptors BMPRIA, BMPRIB, and BMPRII in EOC, benign ovarian tumors, and normal ovarian tissue at the mRNA and protein levels. Immunohistochemistry was used to determine the expression of BMP-2 and its receptors in 100 patients with EOC to analyze their influence on the five-year survival rate and survival time of ovarian cancer patients. Results: (1) The mRNA and protein expression levels of BMP-2, BMPRIB, and BMPRII in ovarian cancer tissue were remarkably lower than those in benign ovarian tumors and normal ovarian tissue, while no significant differences in BMPRIA expression level was found among the three kinds of tissues. (2) The five-year survival rate and the average survival time after surgery of EOC patients with positive expression of BMP-2, BMPRIB, and BMPRII were remarkably higher than those of patients with negative expression of BMP-2, BMPRIB, and BMPRII. BMPRIA expression was not associated with the five-year survival rate or with the average survival time of ovarian cancer patients. Conclusions: BMP-2, BMPRIB, and BMPRII exhibited low expression in EOC tissue, and variation or loss of expression may indicate poor prognosis for ovarian cancer patients.
引用
收藏
页数:6
相关论文
共 23 条
[11]  
Langenfeld EM, 2004, MOL CANCER RES, V2, P141
[12]   The mature bone morphogenetic protein-2 is aberrantly expressed in non-small cell lung carcinomas and stimulates tumor growth of A549 cells [J].
Langenfeld, EM ;
Calvano, SE ;
Abou-Nukta, F ;
Lowry, SF ;
Amenta, P ;
Langenfeld, J .
CARCINOGENESIS, 2003, 24 (09) :1445-1454
[13]   Gene expression profiling of primary cultures of ovarian epithelial cells identifies novel molecular classifiers of ovarian cancer [J].
Le Page, C ;
Ouellet, V ;
Madore, J ;
Ren, F ;
Hudson, TJ ;
Tonin, PN ;
Provencher, DM ;
Mes-Masson, AM .
BRITISH JOURNAL OF CANCER, 2006, 94 (03) :436-445
[14]   Divergence and convergence of TGF-β/BMP signaling [J].
Miyazono, K ;
Kusanagi, K ;
Inoue, H .
JOURNAL OF CELLULAR PHYSIOLOGY, 2001, 187 (03) :265-276
[15]   Isolation and characterization of a novel human NM23-H1B gene, a different transcript of NM23-H1 [J].
Ni, XH ;
Gu, SH ;
Dai, JL ;
Cheng, HP ;
Guo, LC ;
Li, L ;
Ji, CN ;
Xie, Y ;
Ying, K ;
Mao, YM .
JOURNAL OF HUMAN GENETICS, 2003, 48 (02) :96-100
[16]  
Orui H, 2000, J Orthop Sci, V5, P600, DOI 10.1007/s007760070012
[17]   Antiproliferative effects of recombinant human bone morphogenetic protein-2 on human tumor colony-forming units [J].
Soda, H ;
Raymond, E ;
Sharma, S ;
Lawrence, R ;
Cerna, C ;
Gomez, L ;
Timony, GA ;
Von Hoff, DD ;
Izbicka, E .
ANTI-CANCER DRUGS, 1998, 9 (04) :327-331
[18]  
Tada A, 1998, ONCOL REP, V5, P1137
[19]   BONE - FORMATION BY AUTOINDUCTION [J].
URIST, MR .
SCIENCE, 1965, 150 (3698) :893-&
[20]   BMP2 exposure results in decreased PTEN protein degradation and increased PTEN levels [J].
Waite, KA ;
Eng, C .
HUMAN MOLECULAR GENETICS, 2003, 12 (06) :679-684