Literature DB >> 4020386

Tissue distribution of breast cancer-associated antigens defined by monoclonal antibodies.

A E Frankel, D B Ring, F Tringale, S T Hsieh-Ma.   

Abstract

Balb/c mice were immunized with membrane preparations of primary and metastatic breast carcinomas or with live breast cancer cell lines. Sixty-two fusions were performed between immune splenocytes and SP2/0 mouse myeloma cells, and 107 hybridomas were cloned that produced antibody reactive with breast cancer membrane extract, cell lines, and frozen sections, but not with normal tissue membrane extracts or a human fibroblast line. Ninety-four monoclonal antibodies were purified and tested for binding to 16 normal tissue frozen sections and five blood cell types. Thirty-five of the 94 antibodies were also tested on breast cancer sections from 21 patients, 14 breast cancer cell lines, and 11 nonbreast tumor sections. Two of 94 antibodies showed no reactivity to any of the 21 normal tissues or 11 nonbreast neoplasms studied. These two antibodies, 451B7 and 452F2, bound 60% of the breast cancer cell lines and 25% of the breast cancer tissue sections. Eight additional antibodies bound three or fewer of 21 normal tissues. These antibodies bound 25-85% of breast cancer sections, 0-75% of breast cancer cell lines, and many of the nonbreast cancers. A comparison of normal tissues and nonbreast tumors bound by the breast cancer-reactive antibodies indicated that most of the cross-reacting normal tissue structures were epithelial in origin, and that the most cross-reactive nonbreast cancers were those of secondary sex organs (uterus, prostate, ovary).

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Year:  1985        PMID: 4020386

Source DB:  PubMed          Journal:  J Biol Response Mod        ISSN: 0732-6580


  11 in total

1.  Immunocytochemical detection of breast cancer cells in marrow and peripheral blood of patients undergoing high dose chemotherapy with autologous stem cell support.

Authors:  W A Franklin; E J Shpall; P Archer; C S Johnston; S Garza-Williams; L Hami; M A Bitter; R C Bast; R B Jones
Journal:  Breast Cancer Res Treat       Date:  1996       Impact factor: 4.872

2.  Antigen forks: bispecific reagents that inhibit cell growth by binding selected pairs of tumor antigens.

Authors:  D B Ring; S T Hsieh-Ma; T Shi; J Reeder
Journal:  Cancer Immunol Immunother       Date:  1994-07       Impact factor: 6.968

3.  Specific, major histocompatibility complex-unrestricted recognition of tumor-associated mucins by human cytotoxic T cells.

Authors:  D L Barnd; M S Lan; R S Metzgar; O J Finn
Journal:  Proc Natl Acad Sci U S A       Date:  1989-09       Impact factor: 11.205

Review 4.  Immunotoxins against solid tumors.

Authors:  R Pirker
Journal:  J Cancer Res Clin Oncol       Date:  1988       Impact factor: 4.553

5.  A preliminary pharmacokinetic study of 111In-labeled 260F9 anti-(breast cancer) antibody in patients.

Authors:  T W Griffin; F Bokhari; J Collins; M Stochl; M Bernier; M Gionet; D Siebecker; M Wertheimer; E S Giroves; L Greenfield
Journal:  Cancer Immunol Immunother       Date:  1989       Impact factor: 6.968

6.  Response of primary human mammary tumor cell cultures to a monoclonal antibody-recombinant ricin A chain immunotoxin.

Authors:  M J Bjorn; H S Smith; S H Dairkee
Journal:  Cancer Immunol Immunother       Date:  1988       Impact factor: 6.968

7.  Antitumor effects of an immunotoxin made with Pseudomonas exotoxin in a nude mouse model of human ovarian cancer.

Authors:  D J FitzGerald; M C Willingham; I Pastan
Journal:  Proc Natl Acad Sci U S A       Date:  1986-09       Impact factor: 12.779

Review 8.  The use of monoclonal antibody B72.3 in the management of gynecologic malignancies.

Authors:  J Simpson; J Schlom
Journal:  Yale J Biol Med       Date:  1988 Jul-Aug

9.  Purification and characterisation of a breast-cancer-associated glycoprotein not expressed in normal breast and identified by monoclonal antibody 83D4.

Authors:  G Pancino; E Osinaga; C Charpin; D Mistro; J P Barque; A Roseto
Journal:  Br J Cancer       Date:  1991-03       Impact factor: 7.640

10.  Retinoic acid disrupts the Golgi apparatus and increases the cytosolic routing of specific protein toxins.

Authors:  Y N Wu; M Gadina; J H Tao-Cheng; R J Youle
Journal:  J Cell Biol       Date:  1994-05       Impact factor: 10.539

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