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Clinical and Molecular Investigations of the DF3 Breast Cancer-Associated Antigen

  • Daniel F. Hayes
  • Miyako Abe
  • Javed Siddiqui
  • Carlo Tondini
  • Donald W. Kufe

Abstract

The murine MAb DF3 is an IgG1 which was generated against a membrane-enriched cell extract prepared from a human breast carcinoma metastatic to liver (1). Immunoperoxidase studies have demonstrated that MAb DF3 clearly distinguishes malignant and benign breast lesions. Whereas MAb DF3 produces a cytosolic staining pattern in 78% of breast carcinomas, such a pattern is observed in less than 10% of fibrocystic lesions or fibroadenomas (1). In contrast, reactivity of benign breast lesions with MAb DF3 is primarily on the apical borders of the ductules. MAb DF3 also reacts with a variety of non-mammary adenocarcinomas, but, of note, not with colon carcinomas (1). MAb DF3 does not react with tumors of mesenchymal origin. MAb DF3 also reacts with the apical surface of normal breast ductal epithelium, as well as the apical secretory surfaces of several other normal epithelial tissues such as liver, lung, kidney (distal collecting tubules), bladder, testis, uterus, ovary, and sebaceous and sweat glands (2). MAb DF3 does not react with normal adult spleen, colon, bone marrow, heart, stomach, duodenum, skin, or adrenal cortex (2).

Keywords

Metastatic Breast Cancer Sodium Butyrate Benign Breast Lesion Partial cDNA Clone High Molecular Weight Glycoprotein 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer Science+Business Media New York 1989

Authors and Affiliations

  • Daniel F. Hayes
    • 1
  • Miyako Abe
    • 1
  • Javed Siddiqui
    • 1
  • Carlo Tondini
    • 1
  • Donald W. Kufe
    • 1
  1. 1.Laboratory of Clinical PharmacologyDana Farber Cancer InstituteBostonUSA

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