N-cadherin expression in breast cancer: correlation with an aggressive histologic variant - invasive micropapillary carcinoma

被引:73
作者
Nagi, C
Guttman, M
Jaffer, S
Qiao, R
Keren, R
Triana, A
Li, M
Godbold, J
Bleiweiss, IJ
Hazan, RB
机构
[1] Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10461 USA
[2] CUNY Mt Sinai Sch Med, Dept Pathol, New York, NY 10029 USA
[3] CUNY Mt Sinai Sch Med, Dept Oncol Sci, New York, NY 10029 USA
[4] CUNY Mt Sinai Sch Med, Dept Community Med, New York, NY USA
基金
美国国家卫生研究院;
关键词
breast cancer; invasive micropapillary carcinoma; metastasis; N-cadherin; tumor aggressiveness;
D O I
10.1007/s10549-005-7727-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Upregulation of N-cadherin in epithelial tumor cells has been shown to contribute to the invasive/metastatic phenotype. It remains however to be determined whether N-cadherin is increased in human breast cancers with enhanced malignant potential. We examined a large number of invasive breast cancer specimens (n = 114) for N- and E-cadherin. These specimens compared invasive duct carcinomas (IDCs) of varying histologic grades with an aggressive subtype, invasive micropapillary carcinoma of the breast (MPAP), which has a high propensity for lymphatic invasion and lymph node metastasis. Staining scores for N- and E-cadherin were compared between non-MPAP and MPAP IDCs, and between the invasive and ductal carcinoma in situ (DCIS) of each IDC using statistical analysis. We found that N-cadherin was expressed in 76% of MPAP and 52% of non-MPAP carcinomas, and E-cadherin in 57% of MPAP and 36% of non-MPAP tumors. More MPAP (25%) compared to non-MPAP (5%) tumors expressed both cadherins. Of the two cadherins, N-cadherin was significantly associated with MPAP tumors (p = 0.033) compared to E-cad (p = 0.171). Moreover, in the majority of tumors that were positive for N-cadherin, the staining scores were increased in the IDC relative to intraductal components, and this effect was more dramatic in the MPAP carcinomas. This difference for N-cadherin was greater than the corresponding difference for E-cadherin in the MPAP group (p = 0.005), whereas such changes were not significant in the non-MPAP group (p = 0.10). Thus, N-cadherin is associated with tumor aggressiveness and metastatic potential and may contribute to tumor progression.
引用
收藏
页码:225 / 235
页数:11
相关论文
共 47 条
[1]  
Allred DC, 1998, MODERN PATHOL, V11, P155
[2]   LOSS OF EPITHELIAL DIFFERENTIATION AND GAIN OF INVASIVENESS CORRELATES WITH TYROSINE PHOSPHORYLATION OF THE E-CADHERIN BETA-CATENIN COMPLEX IN CELLS TRANSFORMED WITH A TEMPERATURE-SENSITIVE V-SRC GENE [J].
BEHRENS, J ;
VAKAET, L ;
FRIIS, R ;
WINTERHAGER, E ;
VANROY, F ;
MAREEL, MM ;
BIRCHMEIER, W .
JOURNAL OF CELL BIOLOGY, 1993, 120 (03) :757-766
[3]  
Berx G, 1996, ONCOGENE, V13, P1919
[4]   Transforming growth factor-β1 mediates epithelial to mesenchymal transdifferentiation through a RhoA-dependent mechanism [J].
Bhowmick, NA ;
Ghiassi, M ;
Bakin, A ;
Aakre, M ;
Lundquist, CA ;
Engel, ME ;
Arteaga, CL ;
Moses, HL .
MOLECULAR BIOLOGY OF THE CELL, 2001, 12 (01) :27-36
[5]  
Birchmeier W, 1996, CURR TOP MICROBIOL, V213, P117
[6]   PURIFIED N-CADHERIN IS A POTENT SUBSTRATE FOR THE RAPID INDUCTION OF NEURITE OUTGROWTH [J].
BIXBY, JL ;
ZHANG, R .
JOURNAL OF CELL BIOLOGY, 1990, 110 (04) :1253-1260
[7]   Altered expression of adhesion molecules and epithelial-mesenchymal transition in silica-induced rat lung carcinogenesis [J].
Blanco, D ;
Vicent, S ;
Elizegi, E ;
Pino, I ;
Fraga, MF ;
Esteller, M ;
Saffiotti, U ;
Lecanda, F ;
Montuenga, LM .
LABORATORY INVESTIGATION, 2004, 84 (08) :999-1012
[8]   TUMOR INTERACTIONS WITH THE VASCULATURE - ANGIOGENESIS AND TUMOR-METASTASIS [J].
BLOOD, CH ;
ZETTER, BR .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1032 (01) :89-118
[9]  
Bracke ME, 1996, CURR TOP MICROBIOL, V213, P123
[10]   Medical progress - Ductal carcinoma in situ of the breast [J].
Burstein, HJ ;
Polyak, K ;
Wong, JS ;
Lester, SC ;
Kaelin, CM .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (14) :1430-1441