ESTROGEN-RECEPTOR LOCALIZATION IN PARAFFIN SECTIONS BY ENZYME DIGESTION, REPEATED APPLICATIONS OF PRIMARY ANTIBODY, AND IMIDAZOLE

被引:17
作者
ELIAS, JM
HEIMANN, A
CAIN, T
MARGIOTTA, M
GALLERY, F
GOMES, C
机构
[1] Department of Pathology, University Hospital, SUNY, Stony Brook, NY
关键词
Breast cancer; Cytosol assay; Imidazole; Immunocytochemical; Paraffin sections; Steroid receptor measurement;
D O I
10.1179/his.1990.13.1.29
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Measurement of estrogen and progesterone receptors (ER and PR) is very important in selecting treatment for patients with breast cancer because some tumors respond to hormonal treatment. The standard methods for receptor measurements have been the steroid binding assays, especially the biochemical cytosol. These assays have several limitations, among which are that they can not identify tumor cells and they can not be used with routinely fixed and processed tissue. Immunocytochemical techniques with monoclonal antibodies are compatible with the study of receptor content in malignant cells, which is believed to be a good prognosticator of long term survival. One commercial estrogen receptor-immunocytochemical assay kit (ER-ICA) has received Food and Drug Administration approval for diagnostic use; however, it was designed for use on fresh frozen, mildly fixed sections. This study examined the parameters that would permit successful immunostaining with the ER-ICA in routine histologic sections: Enzyme digestion, repeated application of primary antibody, and imidazole in the color development step. Results from ER-ICA performed in paraffin correlated well with those from the cytosol assay, and the technique could be of great value in cases where there is insufficient material for biochemical assay or when frozen material is unavailable. (The J Histotechno 1 13:29, 1990). © 1990 Maney Publishing.
引用
收藏
页码:29 / 33
页数:5
相关论文
共 29 条
  • [11] Sternberger L.A., Hardy P.H., Cuculis J.J., Meyer H., The unlabeled antibody-enzyme method for immunohistochemistry. Preparation and properties of soluble antigen-antibody complex (horseradish peroxidase-antihorseradish peroxidase) and its use in identification of spirochetes, J Histochem Cytochem, 18, (1970)
  • [12] Ku G.F., Fridovich I., Stimulation of the activity of horseradish peroxidase by nitrogenous compounds, J Biol Chem, 263, (1988)
  • [13] Chambers J.T., Kohorn E.L., Schwartz P.E., Estrogen receptor and progestin receptor levels as prognosticators for survival in endometrial cancer, Gynecol Oncol, 31, (1988)
  • [14] Fazekas A.G., Macfarlane J.H., Studies on cytosol and nuclear binding of estradiol in human breast cancer, J Steroid Biochem, 13, (1980)
  • [15] Ottestad L.O., Tvett K.M., Nesland J.M., Et al., An immunocytochemical method for assaying oestrogen receptor in breast cancers. A comparison with the steroid binding assay, Histol Histopathol, 3, (1988)
  • [16] Della Cuna G.R., Principles of endocrine therapy, Handbook of Medical Oncology, (1988)
  • [17] Hanna W., Mobbs B.G., Comparative evaluation of ER-ICA and enzyme immunoassay for the quantitation of estrogen receptors in breast cancer, Am J Clin Pathol, 91, (1989)
  • [18] Straus W., Factors affecting the sensitivity and specificity of the cytochemical reaction for the anti-horseradish peroxidase antibody in lymph tissue sections, J Histochem Cytochem, 28, (1980)
  • [19] Hiort O., Kwan P., Delellis R.A., Immunohistochemistry of estrogen receptor protein in paraffin sections: Effects of enzymatic pretreatment and cobalt chloride intensification, Am J Clin Pathol, 90, (1988)
  • [20] Michels S., Swanson P.E., Frizzera G., Wick M.R., Immuno-staining of leukocyte common antigen using an amplified avi-din-biotin peroxidase complex method and paraffin sections, Arch Pathol Lab Med, 111, (1987)