CELLULAR-TRANSFORMATION BY A UNIQUE ISOLATE OF HUMAN PAPILLOMAVIRUS TYPE-11

被引:0
|
作者
MCGLENNEN, RC
GHAI, J
OSTROW, RS
LABRESH, K
SCHNEIDER, JF
FARAS, AJ
机构
[1] UNIV MINNESOTA, SCH MED,DEPT MICROBIOL,BOX 206, HARVARD ST & E RIVER RD, MINNEAPOLIS, MN 55455 USA
[2] UNIV MINNESOTA, SCH MED, DEPT LAB MED & PATHOL, MINNEAPOLIS, MN 55455 USA
[3] UNIV MINNESOTA, SCH MED, INST HUMAN GENET, MINNEAPOLIS, MN 55455 USA
关键词
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Infection with human papillomavirus type 11 (HPV 11) is associated with benign epithelial proliferations and rarely with malignant and metastasizing tumors. Because of the biological diversity displayed in tissues infected with HPV 11, we have examined the capacity of various isolates of HPV 11 to transform cultured cells and compared their molecular differences by DNA sequence analysis. Five isolates of HPV 11 were examined for their ability to transform primary neonatal rat kidney epithelial cells and NIH 3T3 mouse fibroblasts in DNA transfection experiments using calcium phosphate precipitation. Included in these studies are the prototype isolate from a laryngeal papilloma (HPV 11P); HPV 11VC from a verrucous carcinoma of the penis; HPV 11Epi from the viral episomes of a primary squamous cell carcinoma; and two integrated genomes (HPV 11Int 1 and HPV 11Int 2) of the metastases. Only HPV 11VC cotransfected with the oncogene Ha-ras transformed neonatal rat kidney epithelial cells with an efficiency comparable to that of HPV 16 DNA. HPV 11VC DNA alone transformed NIH 3T3 cells. Analysis of the DNA sequence of HPV 11P and 11VC revealed 16 single nucleotide changes in the upstream regulatory region and open reading frames E1, E2, E4, and E5, five resulting in amino acid substitutions. This is the first demonstration of cellular transformation by a natural isolate HPV 11 DNA in vitro and illustrates that minimal changes in the DNA sequence of certain viruses confer oncogenicity to what are normally nontransforming viruses.
引用
收藏
页码:5872 / 5878
页数:7
相关论文
共 50 条
  • [1] Cellular transformation by a unique isolate of human papillomavirus type 11 (vol 52, pg 5872, 1992)
    McGlennen, RC
    Ghai, J
    Ostrow, RS
    LaBresh, K
    Schneider, JF
    Faras, AJ
    CANCER RESEARCH, 1997, 57 (17) : 3867 - 3867
  • [2] CELLULAR-TRANSFORMATION BY HUMAN PAPILLOMAVIRUS DNA INVITRO
    WATTS, SL
    PHELPS, WC
    OSTROW, RS
    ZACHOW, KR
    FARAS, AJ
    SCIENCE, 1984, 225 (4662) : 634 - 636
  • [3] CELLULAR-TRANSFORMATION BY PAPILLOMAVIRUS ONCOPROTEINS
    MANSUR, CP
    ANDROPHY, EJ
    BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1155 (03) : 323 - 345
  • [4] CO-TRANSFORMATION BY HUMAN PAPILLOMAVIRUS TYPE-6 AND TYPE-11
    STOREY, A
    OSBORN, K
    CRAWFORD, L
    JOURNAL OF GENERAL VIROLOGY, 1990, 71 : 165 - 171
  • [5] SUSCEPTIBILITY OF VARIOUS HUMAN-TISSUES TO TRANSFORMATION INVIVO WITH HUMAN PAPILLOMAVIRUS TYPE-11
    KREIDER, JW
    HOWETT, MK
    STOLER, MH
    ZAINO, RJ
    WELSH, P
    INTERNATIONAL JOURNAL OF CANCER, 1987, 39 (04) : 459 - 465
  • [6] DUPLICATION OF THE UPSTREAM REGULATORY SEQUENCES INCREASES THE TRANSFORMATION POTENTIAL OF HUMAN PAPILLOMAVIRUS TYPE-11
    ROSEN, M
    AUBORN, K
    VIROLOGY, 1991, 185 (01) : 484 - 487
  • [7] INVIVO TRANSFORMATION OF HUMAN-SKIN WITH HUMAN PAPILLOMAVIRUS TYPE-11 FROM CONDYLOMATA ACUMINATA
    KREIDER, JW
    HOWETT, MK
    LILL, NL
    BARTLETT, GL
    ZAINO, RJ
    SEDLACEK, TV
    MORTEL, R
    JOURNAL OF VIROLOGY, 1986, 59 (02) : 369 - 376
  • [8] LABORATORY PRODUCTION INVIVO OF INFECTIOUS HUMAN PAPILLOMAVIRUS TYPE-11
    KREIDER, JW
    HOWETT, MK
    LEUREDUPREE, AE
    ZAINO, RJ
    WEBER, JA
    JOURNAL OF VIROLOGY, 1987, 61 (02) : 590 - 593
  • [9] DETECTION OF HUMAN SERUM ANTIBODIES THAT NEUTRALIZE INFECTIOUS HUMAN PAPILLOMAVIRUS TYPE-11 VIRIONS
    CHRISTENSEN, ND
    KREIDER, JW
    SHAH, KV
    RANDO, RF
    JOURNAL OF GENERAL VIROLOGY, 1992, 73 : 1261 - 1267
  • [10] MONOCLONAL ANTIBODY-MEDIATED NEUTRALIZATION OF INFECTIOUS HUMAN PAPILLOMAVIRUS TYPE-11
    CHRISTENSEN, ND
    KREIDER, JW
    CLADEL, NM
    PATRICK, SD
    WELSH, PA
    JOURNAL OF VIROLOGY, 1990, 64 (11) : 5678 - 5681