OVEREXPRESSION OF HER-2 NEU IN ENDOMETRIAL CANCER IS ASSOCIATED WITH ADVANCED STAGE DISEASE

被引:234
作者
BERCHUCK, A
RODRIGUEZ, G
KINNEY, RB
SOPER, JT
DODGE, RK
CLARKEPEARSON, DL
BAST, RC
机构
[1] DUKE UNIV,DUKE COMPREHENS CANC CTR,DURHAM,NC 27706
[2] DUKE UNIV,DEPT PHARMACOL,DIV GYNECOL ONCOL,DURHAM,NC 27706
[3] DUKE UNIV,DEPT PATHOL,DURHAM,NC 27706
[4] DUKE UNIV,MED CTR,DEPT BIOSTAT,DURHAM,NC 27710
[5] DUKE UNIV,MED CTR,DEPT MED,DURHAM,NC 27710
[6] DUKE UNIV,MED CTR,DEPT MICROBIOL IMMUNOL,DURHAM,NC 27710
关键词
ENDOMETRIAL CANCER; HER-2 NEU ONCOGENE; ENDOMETRIUM;
D O I
10.1016/0002-9378(91)90615-X
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Prior studies have shown that overexpression of HER-2/neu occurs in one third of breast and ovarian cancers and that overexpression is associated with poor prognosis. We used a monoclonal antibody to assess immunohistochemically the level of HER-2/neu expression in normal and malignant endometrium. In 24 normal endometrial samples light to moderate (1+ to 2+) staining for HER-2/neu was seen in the glands, and there was no variation in intensity of staining during the menstrual cycle. Among 95 endometrial adenocarcinomas, nine (9%) were found to have heavier staining for HER-2/neu than was seen in normal endometrium (3+). High expression of HER-2/neu was found in 27% of patients with metastatic disease compared with 4% of patients with disease confined to the uterus (p < 0.005). High HER-2/neu expression also was associated with absence of estrogen receptor (p < 0.005) and with increased mortality from cancer. Further studies are needed to determine the significance of HER-2/neu overexpression in endometrial cancer.
引用
收藏
页码:15 / 21
页数:7
相关论文
共 17 条
[1]  
BACUS SS, 1990, ARCH PATHOL LAB MED, V114, P164
[2]   THE NEU ONCOGENE ENCODES AN EPIDERMAL GROWTH-FACTOR RECEPTOR-RELATED PROTEIN [J].
BARGMANN, CI ;
HUNG, MC ;
WEINBERG, RA .
NATURE, 1986, 319 (6050) :226-230
[3]   MULTIPLE INDEPENDENT ACTIVATIONS OF THE NEU ONCOGENE BY A POINT MUTATION ALTERING THE TRANSMEMBRANE DOMAIN OF P185 [J].
BARGMANN, CI ;
HUNG, MC ;
WEINBERG, RA .
CELL, 1986, 45 (05) :649-657
[4]  
BERCHUCK A, 1990, CANCER RES, V50, P4087
[5]   EPIDERMAL GROWTH-FACTOR RECEPTOR EXPRESSION IN NORMAL AND MALIGNANT ENDOMETRIUM [J].
BERCHUCK, A ;
SOISSON, AP ;
OLT, GJ ;
SOPER, JT ;
CLARKEPEARSON, DL ;
BAST, RC ;
MCCARTY, KS .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1989, 161 (05) :1247-1252
[6]   INFLUENCE OF CYTOPLASMIC STEROID-RECEPTOR CONTENT ON PROGNOSIS OF EARLY STAGE ENDOMETRIAL CARCINOMA [J].
CREASMAN, WT ;
SOPER, JT ;
MCCARTY, KS ;
MCCARTY, KS ;
HINSHAW, W ;
CLARKEPEARSON, DL .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1985, 151 (07) :922-932
[7]   STAGE-SPECIFIC AND TISSUE-SPECIFIC EXPRESSION OF THE NEU ONCOGENE IN RAT DEVELOPMENT [J].
KOKAI, Y ;
COHEN, JA ;
DREBIN, JA ;
GREENE, MI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (23) :8498-8501
[8]   AUTORADIOGRAPHIC LOCALIZATION OF EPIDERMAL GROWTH-FACTOR RECEPTORS TO ALL MAJOR UTERINE CELL-TYPES [J].
LIN, TH ;
MUKKU, VR ;
VERNER, G ;
KIRKLAND, JL ;
STANCEL, GM .
BIOLOGY OF REPRODUCTION, 1988, 38 (02) :403-411
[9]  
MCKENZIE SJ, 1989, ONCOGENE, V4, P543
[10]   DATING THE ENDOMETRIAL BIOPSY [J].
NOYES, RW ;
HERTIG, AT ;
ROCK, J .
FERTILITY AND STERILITY, 1950, 1 (01) :3-25