T. Iizasa et al., SERUM ANTI-P53 AUTOANTIBODIES IN PRIMARY RESECTED NON-SMALL-CELL LUNG-CARCINOMA, Cancer immunology and immunotherapy, 46(6), 1998, pp. 345-349
Mutated p53 proteins accumulate in the nuclei of tumor cells, and anti
-p53 autoantibodies are found in the sera of patients with non-small-c
ell lung carcinoma (NSCLC), We analyzed the correlation among serum an
ti-p53 autoantibodies, immunohistochemical staining for p53, and clini
cal features (age, gender, smoking history, histological type, differe
ntiation, stage, T factor, tumor size, and N factor) in resected non-s
mall-cell lung carcinomas. A total of 62 cases of resected NSCLC were
studied (43 men and 19 women; 33 adenocarcinomas, 21 squamous cell car
cinomas, 8 large-cell carcinomas). Preoperative serum titers of anti-p
53 autoantibodies were detected in 13/62 cases (21.0%). A correlation
between histological type and positive titers of serum p53 autoantibod
ies was seen (large-cell carcinoma versus squamous cell carcinoma and
adenocarcinoma, P = 0.031, chi(2)-test). Out of 25 cases, 10 (40%) wit
h positive immunohistochemical staining for p53 had positive titers, w
hereas 3 positive titers were found in 37 patients with negative immun
ohistochemical staining for p53 (P = 0.0025, chi(2)-test). Serum titer
s of anti-p53 autoanti bodies were present in approximately 20% of the
cases of NSCLC, and overexpression of p53 protein in tumor cells was
detectable in approximately 40%. Serum anti-p53 autoantibodies may be
a clinical parameter for the presence of p53 mutations and p53 overexp
ression in NSCLC patients.