Serum p53 antibody detection in patients with impaired lung function
© Mattioni et al.; licensee BioMed Central Ltd. 2013
Received: 19 June 2012
Accepted: 30 January 2013
Published: 6 February 2013
TP53 gene mutations can lead to the expression of a dysfunctional protein that in turn may enable genetically unstable cells to survive and change into malignant cells. Mutant p53 accumulates early in cells and can precociously induce circulating anti-p53 antibodies (p53Abs); in fact, p53 overexpression has been observed in pre-neoplastic lesions, such as bronchial dysplasia, and p53Abs have been found in patients with Chronic Obstructive Pulmonary Disease, before the diagnosis of lung and other tobacco-related tumors.
A large prospective study was carried out, enrolling non-smokers, ex-smokers and smokers with or without the impairment of lung function, to analyze the incidence of serum p53Abs and the correlation with clinicopathologic features, in particular smoking habits and impairment of lung function, in order to investigate their possible role as early markers of the onset of lung cancer or other cancers. The p53Ab levels were evaluated by a specific ELISA in 675 subjects.
Data showed that significant levels of serum p53Abs were present in 35 subjects (5.2%); no difference was observed in the presence of p53Abs with regard to age and gender, while p53Abs correlated with the number of cigarettes smoked per day and packs-year. Furthermore, serum p53Abs were associated with the worst lung function impairment. The median p53Ab level in positive subjects was 3.5 units/ml (range 1.2 to 65.3 units/ml). Only fifteen positive subjects participated in the follow-up, again resulting positive for serum p53Abs, and no evidence of cancer was found in these patients.
The presence of serum p53Abs was found to be associated with smoking level and lung function impairment, both risk factors of cancer development. However, in our study we have not observed the occurrence of lung cancer or other cancers in the follow-up of positive subjects, therefore we cannot directly correlate the presence of serum p53Abs with cancer risk.
KeywordsImpaired lung function Smoking habits Serum p53 antibodies Biomarkers Lung cancer
Lung cancer is the leading cause of cancer death in the world; in the United States, the death rate is 26% in women and 31% in men . Despite improved therapy, the survival outcome is often limited by late diagnosis, when lung cancer is inoperable, and overall 5-year survival is only 15%. It is, therefore, necessary to search for new diagnostic tools to identify lung cancer in the early stages. Mutations in the TP53 tumour suppressor gene are the most common genetic alterations in human cancers  and most can lead to the expression of mutant p53 proteins with a half-life longer than for the wild type, which then accumulate in cancer cells. Accumulation has also been found in pre-neoplastic lesions and normal tissues surrounding the tumours, suggesting that it occurs early on in cancer progression [3, 4]. The accumulation of p53 can in turn induce circulating anti-p53 antibodies (p53Abs), and in fact there is a close correlation between serum p53Abs and p53 overexpression in the corresponding tissues , so that p53Abs can be considered as early markers for the presence of p53 mutations. Indeed, serum p53Abs were found in patients with Barrett’s metaplasia of the oesophagus evolving into dysplasia and cancer as a consequence of chronic reflux; p53 accumulation especially occurs during transition from low to high grade dysplasia and the appearance of p53Abs may predate the diagnosis of oesophageal carcinoma . These antibodies have also been showed in serum of patients with ulcerative colitis, at high risk of developing colon cancer, and their presence was regarded as an early marker of malignant progression . Further, serum p53Abs were detected in workers occupationally exposed to asbestos, at high risk of cancer, before any clinical evidence of malignancy . Altogether, these data suggest that serum p53Abs may have predictive value for the subsequent development of cancer. In lung cancer, in particular, p53 mutations arise early on, since p53 accumulation was detected in pre-neoplastic lesions such as bronchial dysplasia  and serum p53Abs were found in isolated cases of both heavy smokers and patients with Chronic Obstructive Pulmonary Disease (COPD), at high risk of lung and other tobacco-related cancers, several months before the diagnosis of cancer [10, 11].
Further, a correlation between tobacco smoking and lung cancer has been demonstrated [12, 13] and several studies have shown increased risk of lung cancer in patients with COPD [14, 15], in particular for the squamous histological subtype . Cigarette smoking is the main aetiological factor of both COPD and lung cancer, since cigarette smoke contains elevated concentrations of oxidants and carcinogens that can induce persistent lung inflammation and mutations . Chronic inflammation has been demonstrated to play a central role in cancer pathogenesis  and recent studies have linked Nuclear Factor (NF)-kB, major mediator of inflammation, to carcinogenesis . p53 can suppress inflammatory response by inhibiting NF-kB activity  and since it is often mutated by cigarette smoke, oxidant activation of NF-kB may result in a chronic imbalance in COPD and lung cancer. In addition, p53 can reduce COX-2 expression , another inflammatory mediator involved in lung cancer development and progression , and loss of p53 activity may contribute to the persistent elevation of COX-2 in epithelial stroma and lung cancer cells. Furthermore, COPD frequently shows squamous metaplasia with dysplastic areas at different bronchial levels; metaplasia has been correlated with the response to chronic inflammation and is associated with p53 mutations . Finally, an increased risk of lung cancer has also been reported in patients with restrictive lung disease , only slightly associated with tobacco smoking, in which inflammation of the lung may independently contribute to the pathogenesis of lung cancer.
Therefore, the aim of our work was to investigate, in a large prospective study, the incidence of p53Abs, biomarkers of p53 mutations, in heavy smokers and patients with impaired lung function, at high risk of lung cancer and other cancers, in order to evaluate their relationship with tobacco smoke exposure and chronic airflow limitation, in view of a possible role in the early diagnosis of cancer.
Median (range), years
No. of cigarettes smoked per day
Years since quitting
LFT impairment (obstructive or restrictive)
Serum p53Ab assay
All serum samples were aliquoted, coded, and stored at −80°C until assays were performed. p53Abs were detected by a commercially available, highly specific ELISA kit (Anti-p53 ELISA II kit, PharmaCell, Paris, France), using micro-titre plates coated either with human recombinant p53 protein to detect specific p53Abs, or with control proteins to reveal non-specific interactions. The assay was performed according to the manufacturer’s instructions. All samples were tested blindly, twice in the same assay. Absorbance was measured at 450 nm and 620 nm, using a programmable ELISA reader. p53Ab levels ≥ 1.2 unit/ml were considered as positive, according to the manufacturer’s suggestion; this cut-off was in agreement with other studies .
Usually, p53Abs recognize epitopes in the amino and carboxyl termini of p53 protein, outside the DNA-binding domain where most mutations occur, thus identifying both wild type and mutant p53 proteins; however, p53Abs to certain types of mutant p53 proteins might not bind to the wild type recombinant p53 protein used as antigen in our assay, with the possibility of false negative results. Furthermore, ELISA shows a high specificity, but a low sensitivity for serum antibody detection and novel and more sensitive methods have been developed, such as the particle agglutination assay . However, ELISA still retains its value for diagnostic accuracy and easy performance in routine diagnostic procedures .
Lung function tests
All people were subjected to lung function tests by two spirometers (Altair 1000 and Quark PFT). Lung function tests were carried out according to the American Thoracic Society evaluation methods and the values were reported as percentages of the following parameters: total lung capacity (TLC), forced vital capacity (FVC), forced expiratory volume at first second (FEV1) and FEV1/FVC ratio (Tiffenau index).
Within pulmonary diseases, two types of ventilation defects are identified by lung function tests: obstructive or restrictive type. An obstructive defect of pulmonary ventilation is defined by a Tiffenau index <70%, while stage of obstruction is specified by the FEV1 value as follows: mild, FEV1 ≥70%; moderate, FEV1 <70% but ≥60%; moderately severe, FEV1 <60% but ≥50%; severe, FEV1 <50% but ≥34%; very severe, FEV1 <34%. After evaluation of these parameters, patients were divided into three groups: with mild, moderate or severe (including moderately severe, severe, and very severe) obstructive defects.
A restrictive defect of pulmonary ventilation is characterized by TLC reduction; according to this index, the restrictive defect has been distinguished as: mild, TLC >70%; moderate, TLC from 70% to 60%; moderately severe, TLC <60% but >50%; severe, TLC from 50% to 34%; very severe, TLC <34%. After evaluation of this parameter, patients were divided into three groups: with mild, moderate or severe (including moderately severe, severe, and very severe) restrictive defects.
All statistical analyses were performed by using R . Independent variables were first evaluated for unconditional associations with the dependent variable using a chi-square test for categorical data and t test for continuous data. If a continuous variable did not satisfy the normality assumption, the Wilcoxon rank-sum test was used. Correlations between independent continuous variables were assessed based on Pearson’s correlation coefficient for the normally distributed variables. Correlations between variables that did not satisfy the normality condition were assessed based on Spearman’s rho coefficient. Associations between independent categorical and continuous variables were assessed by the t test, the Wilcoxon rank-sum test, or the exact Wilcoxon rank-sum test, as appropriate. Multivariate analysis was performed on the variables, resulting statistically significantly associated in the univariate analysis. In the univariate/multivariate analysis, P values of <0.05 were considered statistically significant.
Correlation between serum p53Abs and clinicopathologic parameters
(< 58 / ≥ 58)
308 / 328 (48% / 52%)
19 / 15 (56% / 44%)
Male / Female
359 / 281 (56% / 44%)
24 / 11 (69% / 31%)
No. of cigarettes per day
(> 20 / ≤ 20)
197 / 356 (36% / 64%)
19 / 14 (58% / 42%)
(> 40 / ≤ 40)
211 / 341 (38% / 62%)
18 / 15 (55% / 45%)
Moderate-Severe / Normal-Mild
113 / 527 (18% / 82%)
11 / 24 (31% / 69%)
We then considered the correlation between serum p53Abs and impairment of lung function of either the obstructive or restrictive type, classified as mild, moderate, and severe. Twenty one of the 399 subjects with normal lung function tests (5.3%) and fourteen of the 276 patients with altered tests (5.1%) were positive for p53Abs. However, in the latter group, three out of 152 patients with mild (2.0%), eight out of 73 with moderate (11.0%) and three out of 51 with severe (5.9%) impairment of lung function had p53Abs. Then, we examined the correlation between serum p53Abs and, on one hand, subjects with normal lung function or mildly altered tests and, on the other hand, patients with moderate to severe impairment of lung function. A higher rate of serum p53Abs was found as a trend (p = 0.068) in patients with moderate to severe impairment of lung function tests, in comparison to subjects with normal or mildly altered tests (Table 2), this correlation was confirmed by a multivariate analysis (p = 0.045). Furthermore, the multivariate analysis showed the lung function test impairment to be a statistically significant predictor of serum p53Ab detection, but not other parameters, such as age, gender or smoking habit.
Correlation between serum p53Abs and clinicopathologic parameters, distinguishing between subjects with normal or altered LFT
(< 58 / ≥ 58)
(< 58 / ≥ 58)
221/154 (59%/ 41%)
Male / Female
Male / Female
No. of cigarettes per day
(> 20 / ≤ 20)
(> 20 / ≤ 20)
(> 40 / ≤ 40)
(> 40 / ≤ 40)
Correlations between median serum p53Ab levels and clinicopathologic parameters
Median serum p53Ab levels (units/ml)
(< 58 / ≥ 58)
3.5 / 3.6
Male / Female
3.55 / 2.5
No. of cigarettes per day
(> 20 / ≤ 20)
3.5 / 2.5
(> 40 / ≤ 40)
Moderate-Severe / Normal-Mild
5.0 / 8.0
Mild to Severe / Normal
4.6 / 7.8
Finally, due to follow-up loss, only fifteen subjects positive for serum p53Abs were further assessed for the presence of these Abs, with a median follow-up of 24 months (range 6 to 60 months), again resulting positive for p53Abs, and no one has shown any sign of incipient cancer by CT of the chest or other specific examinations, carried out to verify the development of lung cancer or other cancers, such as breast, prostate or colon cancers.
In the present investigation, we detected significant levels of serum p53Abs in 35 (5.2%) out of 675 subjects, including non-smokers, ex-smokers and current smokers, with normal or impaired lung function tests. With regard to smoking status, a trend, although not statistically significant, was found in the frequency of p53Abs, increasing from non-smokers (2.3%) to current smokers (5.5%) and ex-smokers (6.0%); the differences were more evident in subjects with normal lung function tests, while nil in patients with impaired tests. Further, we showed a significant correlation between the presence of serum p53Abs and the number of cigarettes smoked per day, while an increased trend between p53Abs and packs-year was observed. Furthermore, a higher rate of p53Ab positive sera was found as a trend in patients with moderate to severe impairment of lung function, compared to subjects with normal or mildly altered lung function. We also considered the difference in serum p53Abs between subjects with normal lung function and patients with altered lung function with regard to the number of cigarettes smoked per day and packs-year and found a significant correlation of p53Abs with cigarettes smoked per day and an increased trend with packs-year in the normal lung function group, while no correlation was observed in patients with altered lung function tests. Finally, none of the follow-up p53Ab positive subjects showed development of lung cancer or other cancers, such as breast, prostate and colon cancers.
Cigarette smoking is closely correlated with p53 mutations. Husgafvel-Pursiainen and co-authors  observed that the frequency of p53 mutations increased from non-smokers to ex-smokers, reaching the highest rate in current smokers. Li and co-authors  reported a similar trend with frequency of serum p53Abs that increased from non-smokers to ex-smokers and current smokers, with heavy smokers having the highest prevalence. Our study also shows that current smokers (5.5%) and ex-smokers (6.0%) have higher frequencies of serum p53Abs than non-smokers (2.3%). Lubin and co-authors  and Trivers and co-authors  found that serum p53Abs can be detected in ex-smokers and current smokers even 15 months before the diagnosis of lung, breast, and prostate cancers, suggesting that serum p53Abs, closely associated with p53 mutations, may be useful in the early diagnosis of tobacco-related cancers.
Impaired lung function has also been associated with an increased risk of lung cancer. In a meta-analysis, Wasswa-Kintu and co-authors  observed that, independent of cigarette smoking, reduced FEV1 increased lung cancer risk in the general population; in addition, patients with the worst lung function showed the highest risk, while subjects with normal lung function had the lowest risk. Furthermore, even small differences in FEV1 significantly increased the risk of lung cancer; finally, the risk was amplified in women. In a very large prospective study, Purdue and co-authors  found an increased risk of lung cancer in patients with either obstructive or restrictive impairment of lung function. In our investigation, a higher rate of serum p53Abs was found in patients with the worst lung function alterations of either obstructive or restrictive type, thus confirming that p53Abs may be associated with patients at increased risk of lung cancer. Impaired lung function may derive through conditions that increase the risk of lung cancer, such as inflammation of the airways, which plays a role in smokers and patients with asthma or COPD ; on the other hand, inflammatory processes responsible for lung restriction may also contribute to lung cancer pathogenesis . Since p53 can function as an inhibitor of inflammation , mutant p53 proteins may be involved in deregulated inflammation contributing to the pathogenesis of lung cancer and other cancers and then serum p53Abs may be early markers of tumor development in people at high risk of cancer, such as patients with impaired lung function. However, since this study shows there was only a small number of p53Ab positive subjects who complied with the follow-up, and neither lung cancer nor other cancers were observed, we cannot correlate the presence of serum p53Abs with cancer risk.
Other well defined markers of lung cancer are the Kirsten rat sarcoma viral oncogene homolog (KRAS) and Epidermal growth factor receptor (EGFR). KRAS is involved in several signalling pathways and mutations in this gene may lead to cancer development. In fact, KRAS mutations are present up to 30% in non-small cell lung cancers (NSCLC). They are found prevalently on codon 12 and appear early in cancer development; furthermore, in some tumors they have been detected in blood before clinical diagnosis . On the other hand, EGFR is highly expressed in various cancers, including lung cancer. EGFR is a member of the family of EGF tyrosine kinase receptors and upon ligand binding activates several intracellular pathways. A soluble fragment of the EGFR extracellular ligand domain can be detected by ELISA in the blood of cancer patients, including NSCLC patients, and may also be elevated at an early stage of carcinogenesis in asbestosis patients . Thus, KRAS and EGFR might have a role as markers of lung function impairment that may reflect cancer risk. Of interest, other proteins can be used to detect lung function impairment, such as Fibrinogen, Neutrophil gelatinase associated lipocalin, Extracellular newly identified RAGE-binding protein and Heparin-binding EGF-like growth factor, showing significantly different serum levels when comparing mild/moderate and severe/very severe COPD patients to smoking and non-smoking controls .
Detection of serum p53Abs in people at high risk of lung cancer and other cancers, such as heavy smokers and patients with impaired lung function, shows a correlation with cigarettes smoked per day, packs-year and the worst impairment of lung function tests. However, in our study, no correlation was observed between serum p53Abs and cancer risk.
Enzyme-Linked Immunosorbent Assay
Chronic Obstructive Pulmonary Disease
Total Lung Capacity
Forced Vital Capacity
Forced Expiratory Volume at first second
Kirsten rat sarcoma viral oncogene homolog
Epidermal growth factor receptor
Non-small cell lung cancer
Receptor for advanced glycation end products.
The authors acknowledgement Marco Varmi and Mustapha Haoui for their skilful technical assistance. This work was partially supported by the Italian League against Cancer.
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