Home LiteratureArticle Details
PMID: 7819034 Published · ppublish English Journal Article

E-cadherin expression in primary and metastatic thoracic neoplasms and in Barrett's oesophagus.

British journal of cancer ·Vol. 71 ·No. 1 ·1995-01-00 ·Pages 166-72

Bongiorno PF, al-Kasspooles M, Lee SW, Rachwal WJ, Moore JH, Whyte RI, Orringer MB, Beer DG

Abstract

Reduced expression of E-cadherin, a Ca(2+)-dependent cell adhesion molecule present in normal epithelium, has been associated with invasive and metastatic cancer. Immunohistochemistry was used in examining the relationship between E-cadherin expression and stage in 59 oesophageal and 52 lung cancers. Advanced-stage oesophageal cancers were associated with both reduced and disorganised E-cadherin expression (P < 0.01). Advanced-stage lung adenocarcinomas generally exhibited disorganised or reduced E-cadherin expression, but no statistical association between expression pattern and stage was found (P > 0.05). No differences in stage were seen between tumours with reduced or disorganised E-cadherin expression. Altered E-cadherin expression was detected in dysplastic, non-invasive Barrett's oesophagus. Importantly, high-level E-cadherin expression was detected in 17 of 17 lymph nodes containing metastatic cancer. E-cadherin mRNA expression was decreased in tumours with reduced protein expression, but not in tumours with disorganised expression. Expression of alpha-catenin mRNA, an E-cadherin-associated protein, was detected in tissues with altered E-cadherin protein expression. Reduced and disorganised expression of E-cadherin appear to be related to transcriptional and post-translational events respectively, and both appear to represent altered cell adhesion associated with invasion and metastasis in thoracic neoplasms.

MeSH Terms
Adenocarcinoma/chemistry Barrett Esophagus/metabolism Blotting, Northern Cadherins/analysis,genetics Carcinoma, Squamous Cell/chemistry Esophageal Neoplasms/chemistry Humans Immunohistochemistry Lung Neoplasms/chemistry Lymphatic Metastasis RNA, Messenger/analysis Tumor Cells, Cultured
Chemicals
Cadherins RNA, Messenger
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Bongiorno P F
Department of Surgery, University of Michigan Medical School, Ann Arbor 48109.
al-Kasspooles M
Lee S W
Rachwal W J
Moore J H
Whyte R I
Orringer M B
Beer D G
References (33)
33 references, click to expand
  1. DNA sequencing with chain-terminating inhibitors.
    Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463-7 PMID: 271968
  2. E-cadherin: a differentiation marker in thyroid malignancies.
    Cancer Res. 1993 Oct 15;53(20):4987-93 PMID: 8402689
  3. Cadherin cell-adhesion molecules in human epithelial tissues and carcinomas.
    Cancer Res. 1989 Apr 15;49(8):2128-33 PMID: 2702654
  4. Dissecting tumor cell invasion: epithelial cells acquire invasive properties after the loss of uvomorulin-mediated cell-cell adhesion.
    J Cell Biol. 1989 Jun;108(6):2435-47 PMID: 2661563
  5. Expression of the cell-cell adhesion glycoprotein cell-CAM 120/80 in normal human tissues and tumors.
    Am J Pathol. 1989 Jul;135(1):101-10 PMID: 2774055
  6. Cadherins: a molecular family important in selective cell-cell adhesion.
    Annu Rev Biochem. 1990;59:237-52 PMID: 2197976
  7. Altered expression of E-cadherin in gastric cancer tissues and carcinomatous fluid.
    Br J Cancer. 1992 Dec;66(6):1122-30 PMID: 1333788
  8. From cadherins to catenins: cytoplasmic protein interactions and regulation of cell adhesion.
    Trends Genet. 1993 Sep;9(9):317-21 PMID: 8236461
  9. Cadherins in cancer: implications for invasion and metastasis.
    Curr Opin Cell Biol. 1993 Oct;5(5):806-11 PMID: 8240824
  10. Association of the APC gene product with beta-catenin.
    Science. 1993 Dec 10;262(5140):1731-4 PMID: 8259518
  11. Association of the APC tumor suppressor protein with catenins.
    Science. 1993 Dec 10;262(5140):1734-7 PMID: 8259519
  12. E-cadherin and alpha-catenin expression in human esophageal cancer.
    Cancer Res. 1994 Jan 1;54(1):291-6 PMID: 8261454
  13. Cadherin cell adhesion receptors as a morphogenetic regulator.
    Science. 1991 Mar 22;251(5000):1451-5 PMID: 2006419
  14. E-cadherin-mediated cell-cell adhesion prevents invasiveness of human carcinoma cells.
    J Cell Biol. 1991 Apr;113(1):173-85 PMID: 2007622
  15. Down-regulation of E-cadherin expression in Madin Darby canine kidney (MDCK) cells inside tumors of nude mice.
    Int J Cancer. 1991 Apr 1;47(6):922-8 PMID: 2010235
  16. The 102 kd cadherin-associated protein: similarity to vinculin and posttranscriptional regulation of expression.
    Cell. 1991 May 31;65(5):849-57 PMID: 1904011
  17. Expression of the glucocorticoid receptor and K-ras genes in urethan-induced mouse lung tumors and transformed cell lines.
    Exp Lung Res. 1991 Mar-Apr;17(2):371-87 PMID: 2050037
  18. Genetic manipulation of E-cadherin expression by epithelial tumor cells reveals an invasion suppressor role.
    Cell. 1991 Jul 12;66(1):107-19 PMID: 2070412
  19. Evidence for endogenous proteases, mRNA level and insulin as multiple mechanisms of N-cadherin down-regulation during retinal development.
    Development. 1992 Apr;114(4):973-84 PMID: 1618157
  20. Identification of a neural alpha-catenin as a key regulator of cadherin function and multicellular organization.
    Cell. 1992 Jul 24;70(2):293-301 PMID: 1638632
  21. Transcriptional downregulation of gap-junction proteins blocks junctional communication in human mammary tumor cell lines.
    J Cell Biol. 1992 Sep;118(5):1213-21 PMID: 1324944
  22. Expression of the cellular adhesion molecule E-cadherin is reduced or absent in high-grade prostate cancer.
    Cancer Res. 1992 Sep 15;52(18):5104-9 PMID: 1516067
  23. Transformation of cell adhesion properties by exogenously introduced E-cadherin cDNA.
    Nature. 1987 Sep 24-30;329(6137):341-3 PMID: 3498123
  24. E-cadherin expression in primary and metastatic gastric cancer: down-regulation correlates with cellular dedifferentiation and glandular disintegration.
    Cancer Res. 1993 Apr 1;53(7):1690-5 PMID: 8453643
  25. Expression of E-cadherin cell adhesion molecules in human breast cancer tissues and its relationship to metastasis.
    Cancer Res. 1993 Apr 1;53(7):1696-701 PMID: 8453644
  26. Molecular cloning and characterization of the human E-cadherin cDNA.
    Mol Biol Rep. 1993 Feb;17(2):123-8 PMID: 8459805
  27. E-cadherin expression in colorectal cancer. An immunocytochemical and in situ hybridization study.
    Am J Pathol. 1993 Apr;142(4):981-6 PMID: 7682766
  28. Defining E-cadherin-associated protein complexes in epithelial cells: plakoglobin, beta- and gamma-catenin are distinct components.
    J Cell Sci. 1993 Mar;104 ( Pt 3):751-62 PMID: 8267793
  29. Cloning of the human alpha-catenin cDNA and its aberrant mRNA in a human cancer cell line.
    Biochem Biophys Res Commun. 1993 Jun 30;193(3):897-904 PMID: 8323564
  30. Decreased E-cadherin immunoreactivity correlates with poor survival in patients with bladder tumors.
    Cancer Res. 1993 Jul 15;53(14):3241-5 PMID: 8324734
  31. Reduction of E-cadherin levels and deletion of the alpha-catenin gene in human prostate cancer cells.
    Cancer Res. 1993 Aug 1;53(15):3585-90 PMID: 8339265
  32. Expression of the cell-cell adhesion molecule E-cadherin in squamous cell carcinoma of the head and neck.
    Clin Otolaryngol Allied Sci. 1993 Jun;18(3):196-201 PMID: 8365008
  33. Cadherin dysfunction in a human cancer cell line: possible involvement of loss of alpha-catenin expression in reduced cell-cell adhesiveness.
    Cancer Res. 1992 Oct 15;52(20):5770-4 PMID: 1394201
Article Info
Journal
British journal of cancer
Abbr.
Br J Cancer
ISSN
0007-0920
Published
1995-01-00
Pages
166-72
Language
English
Region
England
NLM ID
0370635
PMCID
PMC2033452
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com