p53 Gene mutations and MDM2 amplification are uncommon in primary carcinomas of the uterine cervix

Theodore D. Kessis, Robbert J. Slebos, Sung M. Han, Keerti Shah, Xavier F. Bosch, Nubia Muñoz, Lora Hedrick, Kathleen R. Cho

Research output: Contribution to journalArticlepeer-review

Abstract

The p53 gene is the most frequently altered gene known thus far in a wide variety of human cancers. Inactivation of p53, either through mutation or through interaction with the human papillomavirus (HPV) E6 oncoprotein, is a characteristic feature of all cervical carcinoma cell lines that have been studied. These findings suggest that p53 inactivation is required for cervical carcinoma development and that HPV infection and p53 mutation may be mutually exclusive. We have studied the p53 gene in 35 primary cervical carcinomas. DNA sequence and single strand conformational polymorphism analyses were used to evaluate p53 in 27 squamous carcinomas (25 HPV- positive) and eight adenocarcinomas (four HPV-positive). A missense mutation of p53 was observed in one HPV 16-positive squamous carcinoma, demonstrating that p53 mutations can occur in combination with HPV infection. The HPV- negative tumors all lacked p53 gene mutations. The absence of p53 mutations in HPV-negative cases prompted an assessment of tumors for MDM2 gene amplification. The MDM2 gene encodes a p53 binding protein and has been found to be amplified in some human tumors lacking p53 mutations. MDM2 amplification was not identified in any of the tumors we examined, including four HPV-negative cases. Our findings show that HPV infection and p53 gene mutation are not mutually exclusive and suggest that many HPV-negative carcinomas may arise via a pathway independent of p53 inactivation.

Original languageEnglish (US)
Pages (from-to)1398-1405
Number of pages8
JournalAmerican Journal of Pathology
Volume143
Issue number5
StatePublished - 1993

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

Fingerprint

Dive into the research topics of 'p53 Gene mutations and MDM2 amplification are uncommon in primary carcinomas of the uterine cervix'. Together they form a unique fingerprint.

Cite this