RETRACTED: E6 proteins from diverse cutaneous HPV types inhibit apoptosis in response to UV damage (Retracted article. See APR, 2023)

被引:162
作者
Jackson, S [1 ]
Storey, A [1 ]
机构
[1] Ctr Cutaneous Res, Imperial Canc Res Fund, Skin Tumour Lab, London E1 2AT, England
关键词
HPV; UV; apoptosis; skin;
D O I
10.1038/sj.onc.1203339
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
In addition to their role in anogenital cancer, human papillomaviruses (HPVs) are also involved in the development of a range of cutaneous lesions. HPV types 5 and 8 are associated with the development of skin cancers in individuals with Epidermodysplasia verruciformis (EV). A broad spectrum of NPV types are also commonly found in non-melanoma skin cancers in immunocompromised individuals, such as organ transplant recipients. The skin cancers in EV and immunocompromised patients occur predominantly at body sites exposed to ultra violet (UV) radiation, pointing to a key role for UV in their development, Here rye show that the E6 protein from a range of cutaneous NPV types effectively inhibits apoptosis in response to UV damage, This occurs in both p53 null and wild type cells and does not require p53 degradation.
引用
收藏
页码:592 / 598
页数:7
相关论文
共 44 条
[1]   Roles for p53 in growth arrest and apoptosis: putting on the brakes after genotoxic stress [J].
Amundson, SA ;
Myers, TG ;
Fornace, AJ .
ONCOGENE, 1998, 17 (25) :3287-3299
[2]   NESTED PCR APPROACH FOR DETECTION AND TYPING OF EPIDERMODYSPLASIA VERRUCIFORMIS-ASSOCIATED HUMAN PAPILLOMAVIRUS TYPES IN CUTANEOUS CANCERS FROM RENAL-TRANSPLANT RECIPIENTS [J].
BERKHOUT, RJM ;
TIEBEN, LM ;
SMITS, HL ;
BAVINCK, JNB ;
VERMEER, BJ ;
TERSCHEGGET, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (03) :690-695
[3]  
CAMPBELL C, 1993, CANCER RES, V53, P2697
[4]  
CROOK T, 1991, ONCOGENE, V6, P873
[5]   HIGH-FREQUENCY OF DETECTION OF EPIDERMODYSPLASIA VERRUCIFORMIS-ASSOCIATED HUMAN PAPILLOMAVIRUS DNA IN BIOPSIES FROM MALIGNANT AND PREMALIGNANT SKIN-LESIONS FROM RENAL-TRANSPLANT RECIPIENTS [J].
DEJONGTIEBEN, LM ;
BERKHOUT, RJM ;
SMITS, HL ;
BAVINCK, JNB ;
VERMEER, BJ ;
VANDERWOUDE, FJ ;
TERSCHEGGET, J .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 105 (03) :367-371
[6]   The genomes of three of four novel HPV types, defined by differences of their L1 genes, show high conservation of the E7 gene and the URR [J].
Delius, H ;
Saegling, B ;
Bergmann, K ;
Shamanin, V ;
de Villiers, EM .
VIROLOGY, 1998, 240 (02) :359-365
[7]   THE HUMAN PAPILLOMA VIRUS-16 E7-ONCOPROTEIN IS ABLE TO BIND TO THE RETINOBLASTOMA GENE-PRODUCT [J].
DYSON, N ;
HOWLEY, PM ;
MUNGER, K ;
HARLOW, E .
SCIENCE, 1989, 243 (4893) :934-937
[8]   A comparative analysis of the interactions of the E6 proteins from cutaneous and genital papillomaviruses with p53 and E6AP in correlation to their transforming potential [J].
Elbel, M ;
Carl, S ;
Spaderna, S ;
Iftner, T .
VIROLOGY, 1997, 239 (01) :132-149
[9]   WAF1, A POTENTIAL MEDIATOR OF P53 TUMOR SUPPRESSION [J].
ELDEIRY, WS ;
TOKINO, T ;
VELCULESCU, VE ;
LEVY, DB ;
PARSONS, R ;
TRENT, JM ;
LIN, D ;
MERCER, WE ;
KINZLER, KW ;
VOGELSTEIN, B .
CELL, 1993, 75 (04) :817-825
[10]   HUMAN PAPILLOMAVIRUS TYPE-49, A TYPE ISOLATED FROM FLAT WARTS OF RENAL-TRANSPLANT PATIENTS [J].
FAVRE, M ;
OBALEK, S ;
JABLONSKA, S ;
ORTH, G .
JOURNAL OF VIROLOGY, 1989, 63 (11) :4909-4909