Role of KIT in Early Melanoma Development
Role of KIT in Early Melanoma Development
批准号:
8515973
负责人:
Susana Ortiz Urda
金额:
$12.2万
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:
2011-08-04 至 2016-07-31
关键词:
AreaArtificial skinBiological MarkersCell LineCellsClinicalCritiquesDermisDetectionDevelopmentEarly treatmentEpidermisEventExcisionFaceFactor AnalysisGAB2 geneGenetic EngineeringGoalsGrowthHistologicHomingHumanHutchinson&aposs Melanotic FreckleImatinibImmunodeficient MouseIndividualKIT geneLabelLateralLesionMalignant NeoplasmsMelanoma CellModelingMucous MembraneMusMutationN-CadherinPTPN11 genePathway interactionsPatternPhenotypeRecurrenceResidual stateRoleSignal PathwaySiteSkinSomatic MutationSourceStem Cell FactorSurgical marginsTechniquesTestingTherapeuticTimeVariantWritingXenograft Modelcell motilityin vivoinhibitor/antagonistmeetingsmelanoblastmelanocytemelanomamigrationmutantnovel therapeutic intervention
中文摘要
描述(由申请人提供):本提案的目标是确定最早的黑色素瘤前体,并研究表皮内黑色素瘤进展的机制。最近的研究发现,在原发性黑色素瘤附近的非病变皮肤中,有一种由遗传异常黑色素细胞组成的场效应。有证据表明,这些野细胞可能是局部复发的来源。视场效应似乎仅限于具有小透镜生长模式的黑色素瘤,即表皮内生长模式,其中黑色素细胞在基底表皮内作为单个单位排列,如肢端和小透镜恶性黑色素瘤。这些黑色素瘤类型通常在KIT信号通路中具有激活的遗传改变。由于KIT在黑素细胞迁移和黑素母细胞归巢到基底真皮中起着至关重要的作用,因此假设KIT途径激活代表了启动事件,随后获得了形成临床和组织学可检测病变所需的额外遗传改变。为了验证这一假设,候选人开发了一种早期人类黑色素瘤进展的异种移植模型。具体来说,她将研究基因工程黑素细胞和表达相关KIT突变的黑素细胞植入人皮肤重建体并移植到免疫缺陷小鼠身上的表皮内迁移。同时,候选人将评估KIT抑制剂对表皮内黑色素瘤进展的影响。这些研究将为某些类型的黑色素瘤在明显完全切除后复发的趋势提供解释,并将提供使用KIT抑制剂治疗早期黑色素瘤的可能性。
英文摘要
DESCRIPTION (provided by applicant): The goal of this proposal is to identify the earliest melanoma precursors and to study the mechanisms of intraepidermal melanoma progression. Recent studies have identified a field effect comprised of genetically abnormal melanocytes in the non-lesional skin adjacent to primary melanomas. Evidence suggests that these field cells may be a source of local recurrences. The field effect appears to be confined to melanomas with a lentiginous growth pattern i.e. an intraepidermal growth pattern in which melanocytes are arranged as single units within the basilar epidermis such as acral and lentigo maligna melanomas. These melanoma types frequently have activating genetic alterations in the KIT signaling pathway. Since KIT has an essential role in melanocyte migration and homing of melanoblasts to the basal dermis, the hypothesis is that KIT pathway activation represents the initiating event that is subsequently followed by the acquisition of additional genetic alterations required to form clinically and histologically detectable lesions. To test this hypothesis, the candidate has developed a xenograft model of early human melanoma progression. Specifically, she will study the intraepidermal migration of genetically engineered melanocytes and melanoma cells expressing relevant KIT mutations seeded into human skin reconstructs grafted onto immunodeficient mice. In parallel, the candidate will evaluate the impact of KIT inhibitors on intraepidermal melanoma progression. These studies will provide an explanation for the tendency of certain melanoma types to recur after apparently complete excision and will offer the possibility to use KIT inhibitors to treat early melanoma.
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Role of KIT in Early Melanoma Development
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批准号:8190099
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项目类别:
-
资助金额:$12.2万
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财政年份:2011
-
负责人:Susana Ortiz Urda
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依托单位:
Role of KIT in Early Melanoma Development
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批准号:8312508
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项目类别:
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资助金额:$12.2万
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财政年份:2011
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负责人:Susana Ortiz Urda
-
依托单位:
Role of KIT in Early Melanoma Development
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批准号:8708777
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项目类别:
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资助金额:$12.2万
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财政年份:2011
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负责人:Susana Ortiz Urda
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依托单位:
海外基金