VEGF expression is associated with negative estrogen receptor status in patients with breast cancer

被引:41
作者
Fuckar, D
Dekanic, A
Stifter, S
Mustac, E
Krstulja, M
Dobrila, F
Jonjic, N
机构
[1] Univ Rijeka, Dept Pathol, Sch Med, Rijeka 51000, Croatia
[2] Univ Rijeka, Ctr Hosp, Univ Dept Surg, Rijeka, Croatia
关键词
breast neoplasm; vascular endothelial growth factor A; premenopause; postmenopause; receptors; estrogen; immunohistochemistry;
D O I
10.1177/106689690601400109
中图分类号
R36 [病理学];
学科分类号
100104 [病理学与病理生理学];
摘要
The aim of this study was to analyze the association between vascular endothelial growth factor (VEGF) expression on tumor cells and other clinicopathologic parameters in breast cancer that Could give additional information oil its prognostic significance. Immunohistochemical analysis of expression of VEGF, estrogen (ER) and progesterone receptor (PR), HER-2/neu, and Ki67 was performed in 233 breast cancers. VEGF expression estimated semiquantitatively was correlated with all the above-mentioned parameters as well as with clinicopathologic characteristics of breast cancer such as menopausal status of patients, tumor size, histologic and nuclear grade, vascular invasion, and lymph node status. Most of the tumor cells and some stromal components expressed VEGF. A higher percentage of VEGF-positive tumor cells was present in premenopausal patients and in ER-negative tumors. In postmenopausal patients tumors with a higher expression of VEGF were associated not only with ER-negative but also with HER-2/neu-positive tumor cells. These ER-negative tumors were characterized by a higher proliferative activity. Angiogenic switch as well as proliferative activity of breast cancer cells probably are unfavorably dependent on estrogen activity. This negative correlation between VEGF expression and ER status may not only shed more light on tumor biology but may also have future therapeutic implications.
引用
收藏
页码:49 / 55
页数:7
相关论文
共 30 条
[1]
Ali SH, 2000, CANCER RES, V60, P7094
[2]
Vascular endothelial growth factor is modulated in vascular muscle cells by estradiol, tamoxifen, and hypoxia [J].
Bausero, P ;
Ben-Mahdi, MH ;
Mazucatelli, JP ;
Bloy, C ;
Perrot-Applanat, M .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2000, 279 (05) :H2033-H2042
[3]
Effect of imatinib mesylate on neuroblastoma tumorigenesis and vascular endothelial growth factor expression [J].
Beppu, K ;
Jaboine, J ;
Merchant, MS ;
Mackall, CL ;
Thiele, CJ .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (01) :46-55
[4]
COORDINATE EXPRESSION OF VASCULAR ENDOTHELIAL GROWTH-FACTOR RECEPTOR-1 (FLT-1) AND ITS LIGAND SUGGESTS A PARACRINE REGULATION OF MURINE VASCULAR DEVELOPMENT [J].
BREIER, G ;
CLAUSS, M ;
RISAU, W .
DEVELOPMENTAL DYNAMICS, 1995, 204 (03) :228-239
[5]
Celen O, 2004, NEOPLASMA, V51, P293
[6]
DREISBACH LP, 2002, ASCO ANN M
[7]
ELSON CW, 1991, HISTOPATHOLOGY, V19, P403
[8]
Feige JJ, 2000, B ACAD NAT MED PARIS, V184, P537
[9]
The biology of vascular endothelial growth factor [J].
Ferrara, N ;
DavisSmyth, T .
ENDOCRINE REVIEWS, 1997, 18 (01) :4-25
[10]
Foekens JA, 2001, CANCER RES, V61, P5407