Nitric oxide synthase type 1 expression in human lung cancer and its relation to p53

Med Sci Monit. 2001 Mar-Apr;7(2):218-21.

Abstract

Background: The nitric oxide synthases (NOS) have been observed in human tumour cell lines as well as in solid tumours. Neuronal isoform of NOS (NOS1) was particularly abundant in low-differentiated gynaecological, breast and central nerve system tumours, suggesting that it may characterize poorly differentiated tumours. So far, little is known about expression of the neuronal NOS isoform in non-small cell lung cancer. Our aim was to compare NOS1 expression in non-small lung carcinomas with respect to tumor staging and p53 protein expression.

Material and methods: Thirty-two cases of non-small lung carcinomas of all grades of malignancy and ten control lung specimens with neoplastic lesions were examined. Paraffin-embedded tissues were stained with hematoxylin and eosin, or with antibodies to NOS1 and p53, and evaluated under light microscope.

Results: No statistical correlation between expression of p53, NOS1 and degree od tumour differentiation was observed.

Conclusion: Expression of NOS1 can not serve as a marker for highly malignant tumours in the non-small cell lung carcinomas.

MeSH terms

  • Adult
  • Aged
  • Carcinoma, Non-Small-Cell Lung / enzymology*
  • Carcinoma, Non-Small-Cell Lung / pathology
  • Humans
  • Lung Neoplasms / enzymology*
  • Lung Neoplasms / pathology
  • Middle Aged
  • Nitric Oxide Synthase / metabolism*
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • Tumor Suppressor Protein p53
  • Nitric Oxide Synthase