p53 protein, which accumulates intracellularly in over half of all hum
an rumours, has also been reported to be present in the sera of patien
ts with various malignancies, including lung cancer. Using a quantitat
ive immunoassay, we measured p53 protein concentrations in 216 sera fr
om 114 lung: cancer patients of whom 75 provided matched lung tumour t
issues, which were also assayed for p53 protein. p53 protein levels ab
ove the detection limit of 0.04 ng ml(-1) were detected in only two se
ra from lung cancer patients (0.14 ng ml(-1) and 0.27 ng ml(-1)), but
not in any of 13 sera From non-malignant lung disease patients or in 1
00 sera from normal non-diseased individuals. The presence of these ap
parent traces of serum p53 protein concentrations could not be related
either to the p53 protein expression status of the primary lung rumou
rs or to the tumour stage, grade or histological type. By pretreating
these two sera with anti-p53 antibody linked to solid phase, and by th
e addition of mouse serum to neutralise possible heterophilic antibodi
es, the signals arising from these sera were shown to be non-specific
and possibly caused by heterophilic antibodies. We conclude that our d
ata do not support previous reports of p53 protein in the sera of lung
cancer patients. Since immunoassays are subject to numerous sources o
f interference in serum, including heterophilic antibodies, we suggest
that the results of p53 protein analysis of serum specimens should be
interpreted with caution.