Volume 67, Issue 3 pp. 441-446
Experimental Cancer

Oncogene expression is modulated by recombinant human interferon-β in human breast-cancer cells

Gigliola Sica

Corresponding Author

Gigliola Sica

Institute of Histology and Embryology, Catholic University of the Sacred Heart, Largo Francesco Vito 1, 00168 Rome, Italy

Istituto di Istologia ed Embriologia, Università Cattolica del Sacro Cuore, Facoltà di Medicina e Chirurgia, Largo Francesco Vito 1, 00168 Rome, ItalySearch for more papers by this author
Cristiana Angelucci

Cristiana Angelucci

Institute of Histology and Embryology, Catholic University of the Sacred Heart, Largo Francesco Vito 1, 00168 Rome, Italy

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Luca Marini

Luca Marini

Institute of Histology and Embryology, Catholic University of the Sacred Heart, Largo Francesco Vito 1, 00168 Rome, Italy

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Ferdinando Milazzo

Ferdinando Milazzo

“Cesare Serono” Institute of Research, Via di Valle Caia 22, 00040 Rome, Italy

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Silvia Donini

Silvia Donini

“Cesare Serono” Institute of Research, Via di Valle Caia 22, 00040 Rome, Italy

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Abstract

The effect of recombinant human interferon-β on growth and oncoprotein expression was investigated in several human breast-cancer cell lines with different characteristics. All cell lines tested were sensitive to the antiproliferative action of the drug, regardless of their estrogen sensitivity. The maximal inhibition of cell proliferation was seen after 6 days of treatment. In estrogen-sensitive CG-5 and ZR-75-1 cells, but not in MDA-MB-453 estrogen-insensitive cells, a reduction in c-myc and c-erbB2 oncoproteins occurred after 48–72 hr and became more pronounced after 120–168 hr of treatment, suggesting that this down-regulation is not direct but is mediated by undefined molecular mechanisms. The time-course of the IFN-mediated decrease in oncoproteins seems to indicate that this event is not strictly related to the IFN-regulation of cell proliferation. The expression of c-erbB2 and c-myc was also analyzed, after recombinant human interferon-β treatment, at the mRNA level in CG-5 cells. Surprisingly, no statistically significant variation of c-erbB2 or of c-myc mRNA was found either before or after 120–168 hr. Thus, we surmise that the observed reduction of oncoproteins may be due to post-transcriptional mechanisms. © 1996 Wiley-Liss, Inc.

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