MECHANISMS OF TUMOR-SUPPRESSOR PROTEIN INACTIVATION BY THE HUMAN PAPILLOMAVIRUS E6 AND E7 ONCOPROTEINS

被引:20
作者
HUIBREGTSE, JM [1 ]
SCHEFFNER, M [1 ]
机构
[1] DEUTSCH KREBSFORSCHUNGSZENTRUM, D-69120 HEIDELBERG, GERMANY
来源
SEMINARS IN VIROLOGY | 1994年 / 5卷 / 05期
关键词
HUMAN PAPILLOMAVIRUSES; HPV E6; HPV E7; P53; RETINOBLASTOMA PROTEIN;
D O I
10.1006/smvy.1994.1040
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
There are note, several examples where experimental and epidemiologic data have implied a causative role for viruses in human cancer. Human papillomavirus (HPV) DNA is found in approximately 90% of cervical cancers. Only a subset of the HPV types that infect the anogential tissues, however, are associated with cancer. Interestingly, only the cloned DNA of this subset is capable of immortalizing human primary genital keratinocytes in culture. The oncoproteins of the HPVs are encoded by the E6 and E7 genes. Analogous to the oncoproteins of certain other DNA tumor viruses, the E6 and E7 proteins have been shown to functionally inactivate the tumor suppressor proteins p53 and pRB, respectively. I lie will review what is known of the mechanisms by which the E6 and E7 proteins inactivate these tumor suppressors and the evidence that these activities are related to the transforming capabilities of the HPVs associated with cancer.
引用
收藏
页码:357 / 367
页数:11
相关论文
共 85 条
[1]   ASSOCIATION OF THE HUMAN PAPILLOMAVIRUS TYPE-16 E7 PROTEIN WITH THE S-PHASE-SPECIFIC E2F-CYCLIN-A COMPLEX [J].
ARROYO, M ;
BAGCHI, S ;
RAYCHAUDHURI, P .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (10) :6537-6546
[2]   STRUCTURAL AND TRANSCRIPTIONAL ANALYSIS OF HUMAN PAPILLOMAVIRUS TYPE-16 SEQUENCES IN CERVICAL-CARCINOMA CELL-LINES [J].
BAKER, CC ;
PHELPS, WC ;
LINDGREN, V ;
BRAUN, MJ ;
GONDA, MA ;
HOWLEY, PM .
JOURNAL OF VIROLOGY, 1987, 61 (04) :962-971
[3]   ENHANCED DEGRADATION OF P53 PROTEIN IN HPV-6 AND BPV-1 E6-IMMORTALIZED HUMAN MAMMARY EPITHELIAL-CELLS [J].
BAND, V ;
DALAL, S ;
DELMOLINO, L ;
ANDROPHY, EJ .
EMBO JOURNAL, 1993, 12 (05) :1847-1852
[4]   HUMAN PAPILLOMA-VIRUS DNAS IMMORTALIZE NORMAL HUMAN MAMMARY EPITHELIAL-CELLS AND REDUCE THEIR GROWTH-FACTOR REQUIREMENTS [J].
BAND, V ;
ZAJCHOWSKI, D ;
KULESA, V ;
SAGER, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (01) :463-467
[5]   PAPILLOMAVIRUS POLYPEPTIDE-E6 AND POLYPEPTIDE-E7 ARE ZINC-BINDING PROTEINS [J].
BARBOSA, MS ;
LOWY, DR ;
SCHILLER, JT .
JOURNAL OF VIROLOGY, 1989, 63 (03) :1404-1407
[6]   INDEPENDENT BINDING OF THE RETINOBLASTOMA PROTEIN AND P107 TO THE TRANSCRIPTION FACTOR E2F [J].
CAO, L ;
FAHA, B ;
DEMBSKI, M ;
TSAI, LH ;
HARLOW, E ;
DYSON, N .
NATURE, 1992, 355 (6356) :176-179
[7]   MULTIPLE UBIQUITIN-CONJUGATING ENZYMES PARTICIPATE IN THE IN-VIVO DEGRADATION OF THE YEAST MAT-ALPHA-2 REPRESSOR [J].
CHEN, P ;
JOHNSON, P ;
SOMMER, T ;
JENTSCH, S ;
HOCHSTRASSER, M .
CELL, 1993, 74 (02) :357-369
[8]   DEGRADATION OF NUCLEAR ONCOPROTEINS BY THE UBIQUITIN SYSTEM INVITRO [J].
CIECHANOVER, A ;
DIGIUSEPPE, JA ;
BERCOVICH, B ;
ORIAN, A ;
RICHTER, JD ;
SCHWARTZ, AL ;
BRODEUR, GM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (01) :139-143
[9]   CELL CYCLE-SPECIFIC ASSOCIATION OF E2F WITH THE P130 E1A-BINDING PROTEIN [J].
COBRINIK, D ;
WHYTE, P ;
PEEPER, DS ;
JACKS, T ;
WEINBERG, RA .
GENES & DEVELOPMENT, 1993, 7 (12A) :2392-2404
[10]   DEGRADATION OF P53 CAN BE TARGETED BY HPV E6 SEQUENCES DISTINCT FROM THOSE REQUIRED FOR P53 BINDING AND TRANSACTIVATION [J].
CROOK, T ;
TIDY, JA ;
VOUSDEN, KH .
CELL, 1991, 67 (03) :547-556