Abstract

Somatic cell hybrids between MCF-7 human breast cancer cells and normal immortalized human mammary epithelial cells have been obtained by polyethylene glycol-mediated cell fusion. The hybrid cells are suppressed in their ability to form tumors in nude mice, as well as in traits specific to the tumorigenic MCF-7 parent: growth factor independence, tumor necrosis factor sensitivity, and pS2 gene expression. In addition, they display other characteristics of the "normal" parent, including increased expression relative to the MCF-7 cells of the genes for the extracellular matrix component fibronectin, the intermediate filament keratin 5, and the angiogenesis inhibitor thrombospondin. The levels of keratins 8 and 18 also resemble those of the nontumorigenic parent. These results provide evidence for the existence of tumor suppressor gene products in immortal mammary epithelial cells. We propose a characteristic "suppressed" tumor cell phenotype, which encompasses altered cytoarchitecture, angiogenesis capabilities, and growth factor requirements.

Keywords

BiologyMammary tumorCancer researchCell cultureKeratinExtracellular matrixCancer cellCell fusionAngiogenesisKeratin 5Hepatocyte growth factorCancerKeratin 14Cell biologyBreast cancerGeneGeneticsTransgene

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Publication Info

Year
1990
Type
article
Volume
87
Issue
6
Pages
2314-2318
Citations
72
Access
Closed

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Deborah A. Zajchowski, Vimla Band, Douglas K. Trask et al. (1990). Suppression of tumor-forming ability and related traits in MCF-7 human breast cancer cells by fusion with immortal mammary epithelial cells.. Proceedings of the National Academy of Sciences , 87 (6) , 2314-2318. https://doi.org/10.1073/pnas.87.6.2314

Identifiers

DOI
10.1073/pnas.87.6.2314