Mutations in the TP53 gene and protein expression of p53, MDM 2 and p21/WAF-1 in primary cervical carcinomas with no or low human papillomavirus load

• Published in: British journal of cancer Vol. 78; no. 1; pp. 69 - 72
• Main Authors: HELLAND, A, KARLSEN, F, DUE, E. U, HOLM, R, KRISTENSEN, G, BØRRESEN-DALE, A.-L
• Format: Journal Article
• Language: English
• Published: Basingstoke Nature Publishing Group 01.07.1998; Nature Publishing Group|1
• Subjects: AIDS/HIV; Biological and medical sciences; Cyclin-Dependent Kinase Inhibitor p21; Cyclins - metabolism; Female; Female genital diseases; Genes, p53 - genetics; Gynecology. Andrology. Obstetrics; Humans; Medical sciences; Neoplasm Proteins - metabolism; Nuclear Proteins; Papillomaviridae - isolation & purification; Proto-Oncogene Proteins - metabolism; Proto-Oncogene Proteins c-mdm2; Tumor Suppressor Protein p53 - metabolism; Tumors; Uterine Cervical Neoplasms - genetics; Uterine Cervical Neoplasms - metabolism; Uterine Cervical Neoplasms - virology; Viral Load; Human; Immunohistochemistry; Carcinoma; Papovaviridae; Malignant tumor; Uterine cervix; Gene expression; Carcinogenesis; Female genital diseases; Papillomavirus; Virus; Polymerase chain reaction; Pathology; Human papillomavirus; TP53 Gene; C-Onc gene; Female; Molecular biology; Uterine cervix diseases; Protooncogene; Tumor suppressor gene
• ISSN: 0007-0920; 1532-1827
• DOI: 10.1038/bjc.1998.444

Several studies have focused on the role of p53 inactivation in cervical cancer, either by inactivating mutations in the TP53 gene or by degradation of the p53 protein by human papillomavirus (HPV). In this study, primary cervical carcinomas from 365 patients were analysed for presence of HPV using both consensus primer-sets and type-specific primer-sets. Nineteen samples were determined to have no or low virus load, and were selected for further analyses: mutation screening of the TP53 gene using constant denaturant gel electrophoresis (CDGE) followed by sequencing, and protein expression of p53, MDM2 and p21 using immunohistochemistry (IHC). Mutations in the TP53 gene were found in eight samples (42%). Elevated p53 protein expression was significantly associated with presence of a mutation (P < 0.007). P21 protein expression was detected in 16 of the 19 carcinomas. No p21 expression was seen in normal cervical tissue. Two samples, both with wild-type p53, had elevated MDM2 expression. Compared with a previous study from our group, of mainly HPV-positive cervical carcinomas, in which only one sample was found to contain a TP53 mutation, a significantly higher mutation frequency (P < 0.001) was found among the carcinomas with no or low virus load. Although p53 inactivation pathways are not detected in every tumour, our study supports the hypothesis that p53 inactivation, either by binding to cellular or viral proteins or by mutation, is essential in the development of cervical carcinomas.