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Examination of tumour histopathology and gene expression in a neu / S100A4 transgenic model of metastatic breast cancer
Author(s) -
Simpson Peter T.,
Shoker Balvinder S.,
Barraclough Roger,
Halliwell Nigel,
Rudland Philip S.,
Sibson D. Ross,
Davies Michael P. A.
Publication year - 2003
Publication title -
international journal of experimental pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.671
H-Index - 72
eISSN - 1365-2613
pISSN - 0959-9673
DOI - 10.1046/j.1365-2613.2003.00350.x
Subject(s) - biology , transgene , genetically modified mouse , breast cancer , metastasis , cancer research , pathology , complementary dna , gene , mammary gland , gene expression , cancer , genetics , medicine
Summary. Elevated levels of the calcium‐binding protein S100A4 have been causally linked to the metastatic spread of breast cancer cells in several in vitro and in vivo model systems and, more recently, correlated with patient death in a series of human breast cancer specimens. In transgenic mice expressing MMTV‐ neu transgenes in mammary gland, additional expression of S100A4 transgenes results in an enhanced metastatic capability. Despite this phenotypic difference arising from elevated S100A4, it is now shown that the primary breast tumours in all mice examined are histopathologically very similar and resemble those human tumours associated with elevated c‐ erb B‐2. Using a panel of genes identified by suppression subtractive hybridization of cDNAs from individual primary tumours and a metastasis, some cDNAs were found to exhibit a differential pattern of expression associated with the expression of S100A4 protein (including osteopontin, S100A9, claudin 2 and several Expressed Sequence Tags sequences). Whilst confirming differential expression of these genes, it was demonstrated that individual primary tumours of matched transgenic status, histology and grade exhibit some degree of heterogeneity at the mRNA level by reverse Northern and Northern hybridizations. This intertumour heterogeneity of mRNA level was confirmed by cDNA array analysis and suggests that even in a transgenic model, which exhibits far less variation than the human disease, there may be multiple mechanisms of disease progression.