Prospective evaluation of a novel approach for the use of a quantitative galactose oxidase-Schiff reaction in ductal fluid samples from women with breast carcinoma

被引:8
作者
Chagpar, A
Evelegh, M
Fritsche, HA
Krishnamurthy, S
Hunt, KK
Kuerer, HM
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Surg Oncol, Houston, TX 77030 USA
[2] IMI, Toronto, ON, Canada
[3] Univ Texas, MD Anderson Canc Ctr, Dept Lab Med, Houston, TX 77030 USA
[4] Univ Texas, MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
关键词
nipple aspirate fluid; galactose oxidase-Schiff reaction; breast carcinoma; hue; chroma;
D O I
10.1002/cncr.20311
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. The galactose oxidase-Schiff reaction (GOS) yields positive findings in a number of malignant solid tumors. The goals of the current study were to develop a novel technique for quantifying GOS reactivity in nipple aspirate fluid (NAF) samples from women with invasive breast carcinoma and to assess the clinical utility of the technique in this setting. METHODS. Patients with biopsy-proven unilateral invasive breast carcinoma were eligible for study entry. Before definitive surgery, NAF samples were obtained from healthy breast tissue and malignant breast tissue from 23 women with breast carcinoma. Under blind conditions with respect to clinical data, 10 muL NAF samples were applied to a glass fiber membrane and incubated with 100 muL galactose oxidase and 1 mL Schiff reagent. The stain was developed and the color reaction quantitated by measuring hue (shade) and chroma (intensity) using a spectrophotometer. RESULTS. GOS reactivity was quantitated using two color parameters, hue and chroma. Because chroma varies with concentration, this measurement was adjusted for the concentration of NAF in each sample. After adjustment for NAF concentration, chroma was found to be statistically significantly different in the affected breast tissue sample and the healthy contralateral internal control sample (P = 0.001). CONCLUSIONS. A quantitative measure of GOS reactivity based on spectrophotometric measurement of intensity of color has been developed and was found to be significantly different in the affected breast compared with the unaffected breast in the Current population of patients with breast carcinoma. The preliminary results support further exploration of this novel quantitative test in patients with breast carcinoma. (C) 2004 American Cancer Society.
引用
收藏
页码:2549 / 2554
页数:6
相关论文
共 43 条
[11]   AN EVALUATION OF CA125, CA1 AND PEANUT LECTIN IMMUNOREACTIVITY IN EPITHELIAL OVARIAN NEOPLASMS - CORRELATION WITH HISTOPATHOLOGICAL FEATURES, PROGNOSTIC VARIABLES AND PATIENT OUTCOME [J].
FRIEDLANDER, M ;
LEARY, J ;
RUSSELL, P .
PATHOLOGY, 1988, 20 (01) :38-44
[12]  
Hanisch FG, 1997, HISTOL HISTOPATHOL, V12, P263
[13]  
ITZKOWITZ SH, 1989, CANCER RES, V49, P197
[14]   The promise and pitfalls of breast fluid proteins as markers for cancer detection [J].
King, BL .
CANCER JOURNAL, 2002, 8 (04) :295-297
[15]  
Klein P, 2001, Breast J, V7, P378, DOI 10.1046/j.1524-4741.2001.07601.x
[16]   THE SIGNIFICANCE OF LECTIN RECEPTORS FOR THE EVALUATION OF HORMONE DEPENDENCE IN BREAST-CANCER [J].
KLEIN, PJ ;
VIERBUCHEN, M ;
FISCHER, J ;
SCHULZ, KD ;
FARRAR, G ;
UHLENBRUCK, G .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1983, 19 (01) :839-844
[17]   SECRETION-ASSOCIATED LECTIN-BINDING SITES AS A PARAMETER OF HORMONE DEPENDENCE IN MAMMARY-CARCINOMA [J].
KLEIN, PJ ;
VIERBUCHEN, M ;
WURZ, H ;
SCHULZ, KD ;
NEWMAN, RA .
BRITISH JOURNAL OF CANCER, 1981, 44 (05) :746-748
[18]   PRESENCE AND SIGNIFICANCE OF THE THOMSEN-FRIEDENREICH ANTIGEN IN MAMMARY-GLAND .2. ITS TOPOCHEMISTRY IN NORMAL, HYPERPLASTIC AND CARCINOMA TISSUE OF THE BREAST [J].
KLEIN, PJ ;
NEWMAN, RA ;
MULLER, P ;
UHLENBRUCK, G ;
CITOLER, P ;
SCHAEFER, HE ;
LENNARTZ, KJ ;
FISCHER, R .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1979, 93 (02) :205-214
[19]  
KLEIN PJ, 1981, RECENT RES CANCER, V79, P1
[20]   Nipple aspirate fluid cytology in breast carcinoma [J].
Krishnamurthy, S ;
Sneige, N ;
Thompson, PA ;
Marcy, SM ;
Singletary, SE ;
Cristofanilli, M ;
Hunt, KK ;
Kuerer, HM .
CANCER CYTOPATHOLOGY, 2003, 99 (02) :97-104