K. Oshikawa et Y. Sugiyama, Serum anti-p53 autoantibodies from patients with idiopathic pulmonary fibrosis associated with lung cancer, RESP MED, 94(11), 2000, pp. 1085-1091
Mutations of the tumour suppressor gene p53 lead to accumulation of the mut
ated p53 protein and subsequent production of antoantibodies against p53 pr
oteins, which are also detected in lung cancer. Lung cancer is frequently a
ssociated with idiopathic pulmonary fibrosis (IPF). Therefore, we hypothesi
zed that there might be a relationship between the p53 mutation and high pr
evalence of lung cancer in IPF. To test this hypothesis, we measured serum
p53 antibody levels by an ELISA in various lung diseases including lung can
cer (n=98), IPF (n=46; with lung cancer, n=14 and without lung cancer, n=32
), pulmonary emphysema (PE, n=23) and healthy controls (HC, n=93). The medi
an values of the serum anti-p53 antibody in each group were 8.78, 9.18, 8.0
8 and 4.95 for patients with lung cancer, IPF with lung cancer, IPF without
lung cancer and PE, respectively, and 2.2 for the healthy control group. T
he groups of IPF (with and without lung cancer) showed a similar level of m
edian values to the lung cancer group and a tendency for a higher level tha
n the PE group. When the cut-off value was set at 7.7 according to the 95%
specificity level for normal control, the incidence of positive anti-p53 an
tibody was significantly higher in lung cancer (61.2%), IPF with lung cance
r (57.1%) and IPF without lung cancer (53.1%) than PE (21.7%). These result
s suggest that p53 mutations occur frequently and substantially in IPF, res
ulting in a high prevalence of lung cancer.