Role of ultraviolet radiation in Merkel cell carcinogenesis
Role of ultraviolet radiation in Merkel cell carcinogenesis
批准号:
8110376
负责人:
DAVID M OWENS
金额:
$16.1万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-04-08 至 2013-03-31
关键词:
AcuteBiologyCD 200Cell LineageCellsChronicCutaneousDataDetectionDevelopmentElementsEpidemiologyEpidermisEpithelialEtiologyExhibitsExposure toGenesHomeostasisHumanImmunosuppressionIncidenceInternal Ribosome Entry SiteLaboratoriesLarge T AntigenLesionLymph Node InvolvementMalignant NeoplasmsMerkel CellsMerkel cell carcinomaModelingMusNeoplasm MetastasisNeoplastic Merkel CellNeurosecretory SystemsOncogene ProteinsPathogenesisPatientsPlayPolyomavirusPolyomavirus InfectionsPopulationRisk FactorsRoleSkinSkin CancerSolar EnergyStem cellsSunlightTamoxifenTestingTherapeuticTouch sensationTransgenic MiceUV Radiation ExposureUltraviolet RaysViral OncogeneWorkbasecarcinogenesisdesignkeratinocytemortalitymouse modelnovelprogenitorresponse
中文摘要
描述(由申请人提供):默克尔细胞癌(MCC)是一种罕见但高度侵袭性的皮肤癌,其特征是神经内分泌标志物的表达。MCC特征性地表现出高侵袭和转移倾向;然而,MCC的病因和细胞起源仍然未知。此外,MCC病例的发病率在过去十年中增加了两倍,在检测到淋巴结受累后,不到一半的MCC患者存活一年。人类流行病学数据表明,暴露于紫外线辐射是MCC发展的一个主要危险因素。此外,一种新的人类多瘤病毒,默克尔细胞多瘤病毒(MCPyV),被确定在80%的人皮肤MCC表明,大T抗原转化可能在MCC的发病机制中发挥致病作用。尽管取得了这一进展,但我们对引起MCC的靶细胞的生物学严重缺乏了解,这大大阻碍了确定这种病变的因果因素的努力。本提案中概述的研究是基于我们最近发现的皮肤表皮中的上皮角质形成细胞的离散群体,其充当负责维持正常默克尔细胞谱系的祖细胞库。这种祖细胞群存在于毛状皮肤中的触觉圆顶中,并且在其维持正常默克尔细胞更新的能力方面是独特的。我们的初步研究表明,这些触摸圆顶祖细胞也可能是MCC的靶细胞。为了评估这一点,我们已经基于我们的初步发现产生了一种新的MCC转基因小鼠模型,并且我们将使用该模型来检验以下假设:i)触摸圆顶祖细胞是正常和肿瘤性默克尔细胞的起源细胞,以及ii)紫外线辐射与大T抗原表达的组合足以使默克尔细胞致癌。我们确定MCC关键病理成分的能力将为这些致命癌症的有效治疗策略的发展提供重大飞跃。
公共卫生相关性:长期暴露在阳光下是90%皮肤癌的根本原因。这项建议旨在更好地了解太阳辐射如何影响一种高度侵袭性的皮肤癌默克尔细胞癌的发展。特别是,我们将评估两个重要的危险因素,默克尔细胞癌在人类,紫外线辐射和病毒癌基因,形成默克尔细胞癌在一个新开发的实验小鼠模型的作用。
英文摘要
DESCRIPTION (provided by applicant): Merkel cell carcinoma (MCC) is a rare but highly aggressive form of skin cancer that features the expression of neuroendocrine markers. MCCs characteristically exhibit a high propensity for invasion and metastasis; however, the etiology and cellular origin of MCC remain unknown. Moreover, the incidence of MCC cases has tripled over the last decade with less than half of MCC patients surviving one year following detection of lymph node involvement. Human epidemiological data indicates that exposure to ultraviolet radiation is a major risk factor for MCC development. In addition, a novel human polyomavirus, Merkel cell polyomavirus (MCPyV), was identified in 80% of human cutaneous MCC suggesting that large T antigen transformation may play a causative role in the pathogenesis of MCC. Despite this progress, our severe lack of understanding of the biology of the target cells that give rise to MCC significantly hinders efforts to define the causal elements of this lesion. The studies outlined in this proposal are based on our recent discovery of a discrete population of epithelial keratinocytes in the epidermis of skin that serve as the progenitor cell reservoir responsible for sustaining the normal Merkel cell lineage. This progenitor cell population resides in touch domes in the hairy skin and is unique in its capacity to maintain normal Merkel cell turnover. Our preliminary studies suggest that these touch dome progenitors may also be a target cell for MCC. To assess this, we have generated a novel transgenic mouse model for MCC based on our preliminary findings and we will employ this model to test the hypothesis that i) touch dome progenitor cells are the cells of origin for normal and neoplastic Merkel cells and ii) that ultraviolet radiation in combination with large T antigen expression is sufficient for Merkel cell carcinogenesis. Our ability to pinpoint the critical pathological components of MCC will provide a significant leap forward in the development of effective therapeutic strategies for these fatal cancers.
PUBLIC HEALTH RELEVANCE: Chronic exposure to sunlight is the underlying cause of 90% of skin cancers. This proposal is designed to better understand exactly how solar radiation influences the development of a highly aggressive form of skin cancer called Merkel cell carcinoma. In particular, we will assess the role of two significant risk factors for Merkel cell carcinoma in humans, ultraviolet radiation and viral oncogenes, on the formation Merkel cell carcinoma in a newly develop experimental mouse model.
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