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Certain human papillomavirus (HPV) types are consistently associated with squamous cell carcinoma of the female genital tract. However, these viruses are also detected in histologically normal tissues and only a small proportion of HPV-infected lesions progress to cancer which suggests that additional factors are involved in progression of this disease. In this proposal, the role of cellular oncogenes and growth factors in the pathogenesis of female genital tract cancers, particularly those of the vulva and cervix will be explored. Activated proto-oncogenes have been detected in a variety of tumor cell lines of human origin, as well as in primary human tumors. Yet whether oncogene activation is a necessary step in tumorigenesis is not known. We have analyzed 21 biopsies from 14 patients with colposcopic evidence of condyloma for amplification of the myc or Ha-ras proto- oncogenes by Southern blot hybridization. All specimens were HPV typed. Our results to date indicate that oncogene alterations a) are only detected in HPV-16, not HPV-6 or HPV-11 infected tissues, b) are not detected in premalignant lesions, and c) can occur simultaneously in two biopsies from one patient. We will expand this study to include approximately 100 cervical and vulvar intraepithelial neoplasias to determine if activation (mutation, amplification or rearrangement) of the ras, myc, and erbB/EGF receptor genes in a subset of HPV infected genital tract lesions is involved in the origin or progression of carcinoma of the female genital tract in vivo. We will also study the expression of these genes as well as that of two transforming growth factors, TGF-alpha and TGF-beta by Northern blot hybridization and in situ hybridization using antisense RNA probes. Finally, an in vitro model for papillomavirus-associated transformation using gene transfer techniques will be developed and alterations in the response of HPV-containing cervical epithelial cells to growth factors during carcinogenesis tested. These studies should give us a better understanding of the cellular response to HPV infection and help elucidate the role of human papilloma-viruses in the pathogenesis of genital tract malignancies.
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Regulation of growth and gene expression in human papillomavirus-transformed keratinocytes by transforming growth factor-beta: implications for the control of papillomavirus infection.
通过转化生长因子-β调节人乳头瘤病毒转化的角质形成细胞的生长和基因表达:对控制乳头瘤病毒感染的影响。
DOI: 10.1002/mc.2940060205
发表时间: 1992
期刊: Molecular carcinogenesis
影响因子: 4.6
作者: [Braun,L, Dürst,M, Mikumo,R, Crowley,A, Robinson,M]
通讯作者: Robinson,M
GROWTH REGULATION IN CERVICAL NEOPLASIA
  • 批准号:
    2096983
  • 项目类别:
  • 资助金额:
    $16.12万
  • 财政年份:
    1992
  • 负责人:
    LUNDY A BRAUN
  • 依托单位:
GROWTH REGULATION IN CERVICAL NEOPLASIA
  • 批准号:
    3200461
  • 项目类别:
  • 资助金额:
    $16.05万
  • 财政年份:
    1992
  • 负责人:
    LUNDY A BRAUN
  • 依托单位:
GROWTH REGULATION IN CERVICAL NEOPLASIA
  • 批准号:
    3200459
  • 项目类别:
  • 资助金额:
    $17.61万
  • 财政年份:
    1992
  • 负责人:
    LUNDY A BRAUN
  • 依托单位:
ONCOGENES & GROWTH FACTORS IN HUMAN GYNECOLOGIC CANCERS
  • 批准号:
    3458652
  • 项目类别:
  • 资助金额:
    $10.5万
  • 财政年份:
    1988
  • 负责人:
    LUNDY A BRAUN
  • 依托单位:
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