Elderly Japanese women with cervical carcinoma show higher proportions of both intermediate-risk human papillomavirus types and p53 mutations

被引:11
作者
Nakagawa, S
Yoshikawa, H
Jimbo, H
Onda, T
Yasugi, T
Matsumoto, K
Kino, N
Kawana, K
Kozuka, T
Nakagawa, K
Aoki, M
Taketani, Y
机构
[1] Univ Tokyo, Fac Med, Dept Obstet & Gynecol, Bunkyo Ku, Tokyo 113, Japan
[2] Univ Tokyo, Fac Med, Dept Radiol, Bunkyo Ku, Tokyo 113, Japan
关键词
human papillomavirus; p53; mutation; cervical carcinoma; elderly women;
D O I
10.1038/sj.bjc.6690181
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The p53 mutation has been found only in 0-6% of cervical carcinomas. In light of recent studies demonstrating that mutation of p53 gene was found in over 20% of the patients with vulvar carcinoma, a disease of elderly women and a known human papillomavirus (HPV)related malignancy, we analysed mutation of the p53 gene in 46 women with cervical carcinomas at the age of 60 or more (mean; 71 years, range; 60-96 years). The presence of HPV and its type were analysed by polymerase chain reaction (PCR)-based assay using the consensus primers for L1 region. Mutation of the p53 gene was analysed by PCR-based single-strand conformation polymorphism and DNA sequencing technique. Point mutation of the p53 gene was detected in 5 out of 46 (11%) cervical carcinomas: 1 of 17 (6%) samples associated with high-risk HPVs (HPV 16 and HPV 18) and 4 of 27 samples (15%) with intermediate-risk HPVs (P = 0.36) whereas no mutation was found in 2 HPV negative cases. The mutated residues resided in the selective sequence known as a DNA-binding domain. The immunohistochemistry revealed the overexpression in cancer tissues positive for p53 mutation. All of the observed mutations of the p53 gene were transition type, suggesting that the mutation may be caused by endogenous mutagenesis. Although falling short of statistical significance reduces the strength of the conclusion, data presented here imply that p53 gene mutation, particularly along with intermediate-risk HPV types, may constitute one pathogenetic factor in cervical carcinoma affecting elderly women.
引用
收藏
页码:1139 / 1144
页数:6
相关论文
共 36 条
[11]   CLONING AND EXPRESSION OF THE CDNA FOR E6-AP, A PROTEIN THAT MEDIATES THE INTERACTION OF THE HUMAN PAPILLOMAVIRUS E6 ONCOPROTEIN WITH P53 [J].
HUIBREGTSE, JM ;
SCHEFFNER, M ;
HOWLEY, PM .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (02) :775-784
[12]  
Kagie MJ, 1997, CANCER-AM CANCER SOC, V80, P1228, DOI 10.1002/(SICI)1097-0142(19971001)80:7<1228::AID-CNCR5>3.0.CO
[13]  
2-G
[14]   IMMORTALIZATION OF PRIMARY RAT-CELLS BY HUMAN PAPILLOMAVIRUS TYPE-16 SUBGENOMIC DNA FRAGMENTS CONTROLLED BY THE SV40 PROMOTER [J].
KANDA, T ;
WATANABE, S ;
YOSHIIKE, K .
VIROLOGY, 1988, 165 (01) :321-325
[15]   WILD-TYPE P53 IS A CELL-CYCLE CHECKPOINT DETERMINANT FOLLOWING IRRADIATION [J].
KUERBITZ, SJ ;
PLUNKETT, BS ;
WALSH, WV ;
KASTAN, MB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (16) :7491-7495
[16]   INHIBITION OF P53 DNA-BINDING BY HUMAN PAPILLOMAVIRUS E6 PROTEINS [J].
LECHNER, MS ;
LAIMINS, LA .
JOURNAL OF VIROLOGY, 1994, 68 (07) :4262-4273
[17]  
LEE YY, 1994, ONCOGENE, V9, P1655
[18]   HUMAN PAPILLOMAVIRUS INFECTION OF THE CERVIX - RELATIVE RISK ASSOCIATIONS OF 15 COMMON ANOGENITAL TYPES [J].
LORINCZ, AT ;
REID, R ;
JENSON, AB ;
GREENBERG, MD ;
LANCASTER, W ;
KURMAN, RJ .
OBSTETRICS AND GYNECOLOGY, 1992, 79 (03) :328-337
[19]   P53 IS REQUIRED FOR RADIATION-INDUCED APOPTOSIS IN MOUSE THYMOCYTES [J].
LOWE, SW ;
SCHMITT, EM ;
SMITH, SW ;
OSBORNE, BA ;
JACKS, T .
NATURE, 1993, 362 (6423) :847-849
[20]   PRESENCE AND PERSISTENCE OF HPV INFECTION AND P53 MUTATION IN CANCER OF THE CERVIX UTERI AND THE VULVA [J].
MILDELANGOSCH, K ;
ALBRECHT, K ;
JORAM, S ;
SCHLECHTE, H ;
GIESSING, M ;
LONING, T .
INTERNATIONAL JOURNAL OF CANCER, 1995, 63 (05) :639-645