Esposito V, Baldi A, De Luca A, Micheli P, Mazzarella G, Baldi F, Caputi M, Giordano A
Istituto di Tisiologia e Malattie Respiratorie S. Marcatili, Seconda Universita' degli Studi di Napoli, Naples, Italy.
Hum Pathol. 1997 Feb;28(2):233-7. doi: 10.1016/s0046-8177(97)90112-x.
p53 mutations are among the most frequent genetic alterations reported in human lung cancer. Although the prognostic value of altered p53 expression is still debated, it is accepted widely that estimation of the proliferation rate has an important prognostic role. Moreover, an association between certain types of human lung cancers and tobacco use is well known. Drawing from this background, we investigated the immunohistochemical expression of mutant oncogenic p53 protein, and related it to the smoking history of 61 patients with non-small cell lung carcinoma (NSCLC) and to the expression pattern of proliferating cell nuclear antigen (PCNA), which is considered to be an important negative prognostic factor in several neoplasms. We found p53 overexpression in 22 (36.1%) specimens, including 16 squamous carcinomas (41%) and six (27.2%) adenocarcinomas. PCNA nuclear staining was detected in 98.4% of the specimens, and a significantly higher PCNA expression score was found in all of the p53-positive samples. When the patient survival time was compared, p53 accumulation had a statistically significant negative prognostic value (P < .001). This was supported by a Kaplan-Meier survival percentage plot of immunohistochemically p53-undetectable specimens and p53-detectable specimens. These latter patients had a greatly reduced survival time. A relationship was established between p53 immunohistochemical detection and the smoking history of the patients. None of the specimens from the nonsmoking patients expressed immunohistochemically detectable p53 protein. Altered p53 expression was detected in 40.7% of smoking patients. Our findings support the hypothesis of involvement of p53 mutations in tobacco-induced carcinogensis and indicate that altered p53 expression plays an important prognostic role in NSCLC in smokers.
p53突变是人类肺癌中报道最为频繁的基因改变之一。尽管p53表达改变的预后价值仍存在争议,但普遍认为评估增殖率具有重要的预后作用。此外,某些类型的人类肺癌与吸烟之间的关联是众所周知的。基于这一背景,我们研究了突变致癌性p53蛋白的免疫组化表达,并将其与61例非小细胞肺癌(NSCLC)患者的吸烟史以及增殖细胞核抗原(PCNA)的表达模式相关联,PCNA被认为是几种肿瘤中重要的负面预后因素。我们在22例(36.1%)标本中发现p53过表达,其中包括16例鳞状细胞癌(41%)和6例(27.2%)腺癌。在98.4%的标本中检测到PCNA核染色,并且在所有p53阳性样本中发现PCNA表达评分显著更高。当比较患者生存时间时,p53积累具有统计学上显著的负面预后价值(P < .001)。免疫组化检测不到p53的标本和可检测到p53的标本的Kaplan-Meier生存百分比图支持了这一点。后一组患者的生存时间大大缩短。p53免疫组化检测与患者的吸烟史之间建立了关联。非吸烟患者的标本中无一免疫组化检测到可检测的p53蛋白。在40.7%的吸烟患者中检测到p53表达改变。我们的研究结果支持p53突变参与烟草诱导致癌作用的假说,并表明p53表达改变在吸烟的NSCLC中起重要的预后作用。