Impairment of stimulation by estrogen of insulin-activated nitric oxide synthase in human breast cancer

Int J Cancer. 2002 Jul 20;100(3):261-5. doi: 10.1002/ijc.10482.

Abstract

Nitric oxide (NO) is reported to have several important effects in the control of neoplasm. We have reported before the presence of an insulin-activated constitutive form of membrane-bound nitric oxide synthase (IANOS) in various cells. Since the insulin-induced NO synthesis by IANOS could have important consequences on the pathophysiology of neoplastic cells, the role of estrogen on the activity of IANOS in malignant and nonmalignant breast tissue as well as in erythrocytes in breast cancer patients was determined. It was found that the IANOS activity of nonmalignant breast tissue was maximally stimulated by 4-fold over the basal activity in the presence of physiologic amounts of estrogen (8-32 nM). The enzymic activity was, however, inhibited by estrogen both below and above this range when compared to appropriate controls. In contrast, both the basal IANOS activity and the stimulatory effect of estrogen was markedly impaired in malignant breast tissue and in erythrocytes in these patients. It was also noted that tamoxifen, a widely used nonsteroidal compound in breast cancer, mimicked estrogen both in the stimulation and in the inhibition of IANOS activity in both of the tissues. These results indicated the probable existence of a novel pathway for estrogen effect independent of nuclear receptor for the stimulation of IANOS activity that might have important consequences in breast cancer and suggested that some of the beneficial effects of tamoxifen could be related to its estrogen-mimicking effect on IANOS independent of hormone-responsive elements sequence in the DNA.

MeSH terms

  • Aged
  • Breast Neoplasms / enzymology*
  • Enzyme Activation / drug effects
  • Erythrocytes / enzymology
  • Estrogens / pharmacology*
  • Female
  • Humans
  • Insulin / pharmacology*
  • Middle Aged
  • Nitric Oxide / biosynthesis
  • Nitric Oxide Synthase / metabolism*
  • Tamoxifen / pharmacology

Substances

  • Estrogens
  • Insulin
  • Tamoxifen
  • Nitric Oxide
  • Nitric Oxide Synthase