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Epithelial–mesenchymal interactions in breast cancer: evidence for a role of nuclear localized β‐catenin in carcinoma‐associated fibroblasts
Author(s) -
Verghese Eldo T,
Shenoy Hrishikesh,
Cookson Victoria J,
Green Caroline A,
Howarth Jo,
Partanen R H,
Pollock Steven,
Waterworth Alison,
Speirs Valerie,
Hughes Thomas A,
Hanby Andrew M
Publication year - 2011
Publication title -
histopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.626
H-Index - 124
eISSN - 1365-2559
pISSN - 0309-0167
DOI - 10.1111/j.1365-2559.2011.03917.x
Subject(s) - catenin , carcinogenesis , stromal cell , cancer research , biology , pathology , breast cancer , mesenchymal stem cell , cancer , cancer cell , epithelial–mesenchymal transition , beta catenin , stroma , wnt signaling pathway , medicine , metastasis , immunohistochemistry , signal transduction , microbiology and biotechnology , genetics
Verghese E T, Shenoy H, Cookson V J, Green C A, Howarth J, Partanen R H, Pollock S, Waterworth A, Speirs V, Hughes T A & Hanby A M
(2011) Histopathology 59 , 609–618 Epithelial–mesenchymal interactions in breast cancer: evidence for a role of nuclear localized β‐catenin in carcinoma‐associated fibroblasts Aims: Characteristics of the stroma around tumours are critical in defining the behaviour of cancers. β‐Catenin is well established as a critical regulator of carcinogenesis, acting as a transcriptional co‐activator in the nuclei of epithelial cancer cells. We have examined the prevalence and influence of nuclear β‐catenin within the stromal fibroblasts of breast cancer. Methods and results: We examined β‐catenin expression in 201 breast cancers and adjacent normal tissue. Fibroblasts expressing nuclear β‐catenin were present in a significantly greater proportion of tumour tissues than normal tissues. The presence of fibroblasts with nuclear β‐catenin in tumours correlated with survival; tumours with prevalent positive fibroblasts were associated significantly with relatively good prognoses. Functional studies to examine influences of fibroblasts with nuclear β‐catenin, showed fibroblasts transfected to allow overexpression of β‐catenin were capable of inducing increases in both proliferation and invasion of breast cancer cell lines. Conclusion: The presence of fibroblasts with nuclear β‐catenin in tumours is a good prognostic indicator, although in the context of tissue culture models these cells can increase the growth and metastatic potential of cancer cells. These apparently paradoxical observations underline the complexity of epithelial–stromal signalling within tumours and highlight an area for further study.