Literature DB >> 2835154

Transcription of genes of the carcinoembryonic antigen family in malignant and nonmalignant human tissues.

D Cournoyer1, N Beauchemin, D Boucher, S Benchimol, A Fuks, C P Stanners.   

Abstract

Normal and diseased human tissues were analyzed for the transcription of genes of the carcinoembryonic (CEA) family. Epithelial tissues of colonic origin, whether malignant or normal, all express two closely related mRNA species of 3.0- and 3.5-kilobase mRNA which code for CEA. Only tissues of colonic origin were found to express these CEA-specific transcripts. Colon carcinomas consistently express a 2.6-kilobase mRNA species as well which codes for nonspecific cross-reacting antigen. Nonneoplastic colon mucosas, on the other hand, express lower or nondetectable levels of this transcript. Most breast carcinomas produce only the nonspecific cross-reacting antigen mRNA, whereas leukocytes of chronic myelogeneous leukemia express both nonspecific cross-reacting antigen mRNA and a 2.3-kilobase mRNA corresponding to a yet undefined gene of the CEA family. Thus the multiple CEA-like products reported to be produced by these tissues correspond to only four different mRNA species coding for three different peptides. These data suggest a less complex organization of the CEA family than was previously suspected and point to posttranscriptional modifications, such as variable patterns of glycosylation, as the likely reason for much of the observed complexity in CEA-like glycoproteins.

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Year:  1988        PMID: 2835154

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


  11 in total

1.  A colonic tissue architecture assay applied to human colon carcinoma cells.

Authors:  C Ilantzis; C P Stanners
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2.  Spectrum of carcinoembryonic antigen immunoreactivity from isolated ductal hyperplasias to atypical hyperplasias associated with infiltrating ductal breast cancer.

Authors:  F C Schmitt; L Andrade
Journal:  J Clin Pathol       Date:  1995-01       Impact factor: 3.411

Review 3.  Adhesion molecules and their role in cancer metastasis.

Authors:  R M Lafrenie; M R Buchanan; F W Orr
Journal:  Cell Biophys       Date:  1993 Aug-Dec

4.  Characterization of genetically modified T-cell receptors that recognize the CEA:691-699 peptide in the context of HLA-A2.1 on human colorectal cancer cells.

Authors:  Maria R Parkhurst; Jayne Joo; John P Riley; Zhiya Yu; Yong Li; Paul F Robbins; Steven A Rosenberg
Journal:  Clin Cancer Res       Date:  2009-01-01       Impact factor: 12.531

5.  Human lung tumor-associated antigen identified as an extracellular matrix adhesion molecule.

Authors:  F A Chen; E A Repasky; R B Bankert
Journal:  J Exp Med       Date:  1991-05-01       Impact factor: 14.307

6.  Carcinoembryonic antigen, a human tumor marker, cooperates with Myc and Bcl-2 in cellular transformation.

Authors:  R A Screaton; L Z Penn; C P Stanners
Journal:  J Cell Biol       Date:  1997-05-19       Impact factor: 10.539

7.  Detection of mRNAs of carcinoembryonic antigen and nonspecific cross-reacting antigen genes in colorectal adenomas and carcinomas by in situ hybridization.

Authors:  T Higashide; Y Hinoda; J Itoh; H Takahashi; Y Satoh; Y Ibayashi; K Imai; A Yachi
Journal:  Jpn J Cancer Res       Date:  1990-11

8.  Expression of carcinoembryonic antigen (CEA) and nonspecific crossreacting antigen (NCA) in gastrointestinal cancer; the correlation with degree of differentiation.

Authors:  Y Kodera; K Isobe; M Yamauchi; T Satta; T Hasegawa; S Oikawa; K Kondoh; S Akiyama; K Itoh; I Nakashima
Journal:  Br J Cancer       Date:  1993-07       Impact factor: 7.640

9.  Nonspecific crossreacting antigen (NCA) is a major member of the carcinoembryonic antigen (CEA)-related gene family expressed in lung cancer.

Authors:  T Hasegawa; K Isobe; Y Tsuchiya; S Oikawa; H Nakazato; I Nakashima; K Shimokata
Journal:  Br J Cancer       Date:  1993-01       Impact factor: 7.640

10.  Human carcinoembryonic antigen, an intercellular adhesion molecule, blocks fusion and differentiation of rat myoblasts.

Authors:  F J Eidelman; A Fuks; L DeMarte; M Taheri; C P Stanners
Journal:  J Cell Biol       Date:  1993-10       Impact factor: 10.539

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