The p53 gene is well known as a tumour suppressor gene. In addition, t
he mutated p53 gene is detected in a variety of human cancers includin
g lung cancer, and is considered as an oncogene. Lung cancer is also f
requently associated with interstitial lung diseases. Therefore. it ma
y be possible to hypothesize that there might be some abnormality of p
53 gene in interstitial lung diseases. This work examined the relation
ship between the p53 protein and gene in lung tissues of 28 patients w
ith interstitial lung diseases. Among 28 patients, 13 cases were patho
logically diagnosed to have usual interstitial pneumonia (UIP), 12 cas
es were diagnosed as having collagen vascular lung diseases, and three
cases were diagnosed to have a non-specific interstitial pneumonia. T
wenty-three tissue samples were obtained by open lung biopsy and five
samples were taken by autopsy. Paraffin-embedded tissues were treated
by microwave, and stained with an anti-p53 antibody (DO7) by the Avidi
n-Biotin-Peroxidase (ABC) method. In selected patients, mutations in e
xons 5-8 of the p53 gene were also examined by single-strand conformat
ion polymorphism (SSCP) analysis and DNA sequence. In addition, the pr
esence of anti-p53 antibodies in patients' sera was screened for by EL
ISA. Fifteen samples (53.6%) revealed overexpression of the p53 protei
n in the nuclei of alveolar epithelial cells. However, SSCP or sequenc
e analysis, which was performed in 13 tissues, showed no mutations in
exons 5-8 of the p53 gene. In conclusion, p53 proteins were overexpres
sed in interstitial lung diseases, and the expressed p53 protein was c
onsidered to be wild-type. This wild-type p53 protein may play a role
in blocking the transformation of proliferative epithelial cells.