Human papillomaviruses and their role in cervical cancer

被引:87
作者
Dell, C [1 ]
Gaston, K [1 ]
机构
[1] Univ Bristol, Sch Med Sci, Dept Biochem, Bristol BS8 1TD, Avon, England
关键词
cervical cancer; papillomavirus; gene expression; viral oncogene; early protein; tumour suppressor protein; p53; Rb;
D O I
10.1007/PL00000827
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human papillomaviruses (HPVs) have been linked to a variety of human diseases, most notably cancer of the cervix, a disease responsible for at least 200,000 deaths per year worldwide. Over 100 different types of HPV have been identified and these can be divided into two groups. Low-risk HPV types are the causative agent of benign warts. High-risk HPV types are associated with cancer. This review focuses on the role of high-risk HPV types in cervical tumorigenesis. Recent work has uncovered new cellular partners for many of the HPV early proteins and thrown light on many of the pathways and processes in which these viral proteins intervene. At the same time, structural and biochemical studies are revealing the molecular details of viral protein function. Several of these new avenues of research have the potential to lead to new approaches to the treatment and prevention of cervical cancer.
引用
收藏
页码:1923 / 1942
页数:20
相关论文
共 264 条
[1]  
ABDULKARIM FW, 1982, OBSTET GYNECOL, V60, P210
[2]   The transmembrane domain of the E5 oncoprotein contains functionally discrete helical faces [J].
Adduci, AJ ;
Schlegel, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (15) :10249-10258
[3]   A fluorescence anisotrophy study of DNA binding by HPV-11 E2C protein: A hierarchy of E2-binding sites [J].
Alexander, KA ;
Phelps, WC .
BIOCHEMISTRY, 1996, 35 (30) :9864-9872
[4]   Identification of domains of the HPV11 E1 protein required for DNA replication in vitro [J].
Amin, AA ;
Titolo, S ;
Pelletier, A ;
Fink, D ;
Cordingley, MG ;
Archambault, J .
VIROLOGY, 2000, 272 (01) :137-150
[5]   VACUOLAR H+-ATPASE MUTANTS TRANSFORM CELLS AND DEFINE A BINDING-SITE FOR THE PAPILLOMAVIRUS E5 ONCOPROTEIN [J].
ANDRESSON, T ;
SPARKOWSKI, J ;
GOLDSTEIN, DJ ;
SCHLEGEL, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (12) :6830-6837
[6]  
[Anonymous], 1995, American Cancer Society Textbook of Clincal Oncology
[7]   The human papillomavirus type 16 E7 gene product interacts with and trans-activates the AP1 family of transcription factors [J].
Antinore, MJ ;
Birrer, MJ ;
Patel, D ;
Nader, L ;
McCance, DJ .
EMBO JOURNAL, 1996, 15 (08) :1950-1960
[8]   Structure of the intact transactivation domain of the human papillomavirus E2 protein [J].
Antson, AA ;
Burns, JE ;
Moroz, OV ;
Scott, DJ ;
Sanders, CM ;
Bronstein, IB ;
Dodson, GG ;
Wilson, KS ;
Maitland, NJ .
NATURE, 2000, 403 (6771) :805-809
[9]  
Arany I, 1995, ANTICANCER RES, V15, P2865
[10]   The relative ability of human papillomavirus type 6 and human papillomavirus type 16 E7 proteins to transactivate E2F-responsive elements is promoter- and cell-dependent [J].
Armstrong, DJ ;
Roman, A .
VIROLOGY, 1997, 239 (01) :238-246