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Review
. 2001;3(5):289-93.
doi: 10.1186/bcr309. Epub 2001 Jun 28.

The E-cadherin/catenin complex: an important gatekeeper in breast cancer tumorigenesis and malignant progression

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Review

The E-cadherin/catenin complex: an important gatekeeper in breast cancer tumorigenesis and malignant progression

G Berx et al. Breast Cancer Res. 2001.

Abstract

E-cadherin is a cell-cell adhesion protein fulfilling a prominent role in epithelial differentiation. Data from model systems suggest that E-cadherin is a potent invasion/tumor suppressor of breast cancer. Consistent with this role in breast cancer progression, partial or complete loss of E-cadherin expression has been found to correlate with poor prognosis in breast cancer patients. The E-cadherin gene (CDH1) is located on human chromosome 16q22.1, a region frequently affected with loss of heterozygosity in sporadic breast cancer. Invasive lobular breast carcinomas, which are typically completely E-cadherin-negative, often show inactivating mutations in combination with loss of heterozygosity of the wild-type CDH1 allele. Mutations were found at early noninvasive stages, thus associating E-cadherin mutations with loss of cell growth control and defining CDH1 as the tumor suppressor for the lobular breast cancer subtype. Ductal breast cancers in general show heterogeneous loss of E-cadherin expression, associated with epigenetic transcriptional downregulation. It is proposed that the microenvironment at the invasive front is transiently downregulating E-cadherin transcription. This can be associated with induction of nonepithelial cadherins.

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References

    1. Thoreson MA, Anastasiadis PZ, Daniel JM, Ireton RC, Wheelock MJ, Johnson KR, Hummingbird DK, Reynolds AB. Selective uncoupling of p120ctn from E-cadherin disrupts strong adhesion. J Cell Biol. 2000;148:189–201. - PMC - PubMed
    1. Behrens J. Cadherins and catenins: Role in signal transduction and tumor progression. Cancer Metastasis Rev. 1999;18:15–30. - PubMed
    1. Frixen UH, Behrens J, Sachs M, Eberle G, Voss B, Warda A, Löchner D, Birchmeier W. E-cadherin-mediated cell–cell adhesion prevents invasiveness of human carcinoma cells. J Cell Biol. 1991;113:173–185. - PMC - PubMed
    1. Meiners S, Brinkmann V, Naundorf H, Birchmeier W. Role of morphogenetic factors in metastasis of mammary carcinoma cells. Oncogene. 1998;16:9–20. doi: 10.1038/sj/onc/1201486. - DOI - PubMed
    1. Perl AK, Wilgenbus P, Dahl U, Semb H, Christofori G. A causal role for E-cadherin in the transition from adenoma to carcinoma. Nature (London) 1998;392:190–193. - PubMed