Hormonal regulation of c-erbB-2 oncogene expression in breast cancer cells

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Abstract

Expression of the c-erbB-2 (neu, HER-2) oncogene is found to be subjected to hormonal and developmental regulation in normal as well as neoplastic mammary cells. We have previously reported that estrogens inhibit c-erbB-2 expression at both the mRNA and protein level in estrogen receptor (ER)-positive, but not in ER-negative, breast cancer cell lines. Reversion of c-erbB-2 inhibition is seen with tamoxifen. The effect on c-erbB-2 expression of several other hormones and factors, which influence mammary cell growth and differentiation, has been studied. Our observations indicate that, in normal and neoplastic mammary cells, c-erbB-2 expression is inversely related to cell proliferation. While estrogens, anti-estrogens and cAMP clearly regulate c-erbB-2 mRNA levels, epidermal growth factor dramatically decreases the c-erbB-2 protein without affecting the level of c-erbB-2 mRNA. Therefore, different signals converging in terms of cell proliferation regulate c-erbB-2 expression by different molecular mechanisms.

References (26)

  • C.I. Bargmann et al.

    The neu oncogene encodes an epidermal growth factor receptor-related protein

    Nature

    (1986)
  • T. Yamamoto et al.

    Similarity of protein encoded by the human c-erbB-2 gene to epidermal growth factor receptor

    Nature

    (1986)
  • R. Lupu et al.

    Direct interaction of a ligand for the erbB2 oncogene product with the EGF receptor and p185erbB2

    Science

    (1990)
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