Literature DB >> 2400995

Tumor-associated antigens common to humans and chemically induced colonic tumors of the rat.

J D Shetye1, C A Rubio, U Harmenberg, J Ware, A Duvander, H T Mellstedt.   

Abstract

The expression of human tumor-associated antigens CO17-1A, GA73-3, BR55-2, GICA 19-9, and CA50 and of carcinoembryonic antigen was immunohistochemically studied in the colonic mucosa of 70 Sprague-Dawley rats. Fifty were treated with 1,2-dimethylhydrazine (DMH) (with EDTA as a vehicle), ten were treated with EDTA only, and ten were untreated normal rats. The tumors were histogenetically divided as: (a) adenocarcinomas arising from villous adenomas; (b) adenocarcinomas arising from lymphoid-associated mucosa (LAM); and (c) adenocarcinomas arising in flat mucosa. Of 44 colonic adenocarcinomas, BR55-2 was expressed in 41 tumors, CO17-1A in 40 tumors, GA73-3 in 38 tumors, and GICA 19-9 in 38 tumors. CA50 and carcinoembryonic antigen were not expressed in the tumors. The highest antigenic expression (number of cells) was observed in adenocarcinomas arising in villous adenomas and the lowest in those arising in flat mucosa. Adenocarcinomas arising in LAM had an intermediate expression. The expression of these antigens had no correlation to the localization of the tumor and to the differentiation. The expression of these antigens was similar in the non-lymphoid-associated normal colonic mucosa of the untreated, EDTA-treated, and DMH-treated rats. In DMH-treated rats, LAM demonstrated increased expression (number of cells) and increased staining intensity of these tumor-associated antigens. In six of the 50 DMH-treated rats, only LAM expressed carcinoembryonic antigen. CA50 was not expressed in the normal colon of untreated, of EDTA-treated, and of DMH-treated rats, nor was it in DMH-induced tumors. None of the tumor-associated antigens (GICA 19-9 and CA50 and carcinoembryonic antigen) was detected in serum. It is concluded that this animal model would be of value in the preclinical evaluations of monoclonal antibodies for therapy in humans.

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Year:  1990        PMID: 2400995

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  4 in total

1.  Inhibition of tumor progression and neoangiogenesis using cyclic RGD-peptides in a chemically induced colon carcinoma in rats.

Authors:  Jörg Haier; Ulrike Goldmann; Birgit Hotz; Norbert Runkel; Ulrich Keilholz
Journal:  Clin Exp Metastasis       Date:  2002       Impact factor: 5.150

2.  Ear tumours induced by experimental carcinogenesis in the rat: excision prevents early death.

Authors:  J Shetye; T Mathiesen; J Fagerberg; C Rubio
Journal:  Int J Colorectal Dis       Date:  1994-08       Impact factor: 2.571

3.  Expression of an antigen homologous to the human CO17-1A/GA733 colon cancer antigen in animal tissues.

Authors:  J Zaloudik; S Basak; M Nesbit; D W Speicher; W H Wunner; E Miller; C Ernst-Grotkowski; R Kennedy; L P Bergsagel; T Koido; D Herlyn
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

4.  Corrupted colonic crypt fission in carcinogen-treated rats.

Authors:  Carlos A Rubio
Journal:  PLoS One       Date:  2017-03-08       Impact factor: 3.240

  4 in total

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