Mechanism of keratinocyte RXRalpha mediated melanoma skin cancer development

角质形成细胞RXRα介导黑色素瘤皮肤癌发生的机制

• 批准号: 7584410
• 负责人: Arup K. Indra
• 金额: $ 32.02万
• 依托单位: OREGON STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-01-08 至 2013-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7584410
• 关键词: Adhesions; Automobile Driving; Biological; Biology; CDKN2A gene; Carcinogens; Cell Cycle Regulation; Cell physiology; Cells; Characteristics; Childhood; Communities; Cutaneous Melanoma; Cyclin-Dependent Kinase 4; Data; Development; Disease; Endothelin; Endothelin-1; Environmental Risk Factor; Epidermis; Event; Exhibits; Fibroblast Growth Factor; Fibroblast Growth Factor 2; Frequencies; Future; Generations; Genes; Genetic; Goals; Growth; Growth Factor; Health; Heterodimerization; Homeostasis; Human; Induced Mutation; Knowledge; Laboratories; Lead; Malignant Neoplasms; Mediating; Melanocyte stimulating hormone; Modality; Molecular; Mus; Mutant Strains Mice; Mutation; Neonatal; Neoplasm Metastasis; Nevus; Nuclear Receptors; Outcome; Pathway interactions; Positioning Attribute; Predisposition; Prevention strategy; Principal Investigator; Process; Protocols documentation; RXR; Regulation; Regulatory Pathway; Research; Resistance; Resources; Risk Factors; Role; Signal Pathway; Signal Transduction; Skin; Skin Cancer; Stem Cell Factor; Stimulation of Cell Proliferation; Sun Exposure; Therapeutic; Therapeutic Intervention; Transcriptional Regulation; UV induced; Ultraviolet Rays; United States; Wild Type Mouse; Work; base; cancer therapy; chemical carcinogenesis; cytokine; design; expectation; in vivo; innovation; interest; keratinocyte; malignant phenotype; melanocyte; melanoma; member; migration; mouse model; novel; novel therapeutics; paracrine; programs; public health relevance; ultraviolet; ultraviolet irradiation

DESCRIPTION (provided by applicant): Malignant melanoma is one of the fastest increasing cancers in the United States and no curative treatment is yet available. Solar ultraviolet (UV) radiation, especially childhood sun exposure is an important etiological risk factor of melanoma. Retinoid X Receptor a (RXRa), a member of the nuclear receptor (NR) superfamily, is a central coordinator for transducing diverse cellular signals. In the context of studying the role of RXRa in skin, we have discovered an unexpected and novel role for this NR in melanomagenesis: RXRa[ep-/-] mice, specifically lacking RXRa in epidermal keratinocytes, develop melanocytic growths (MGs) resembling melanoma at high frequency when subjected to a two-step chemical carcinogenesis protocol (DMBA+TPA). Our results suggest that RXRa may regulate a keratinocyte ? melanocyte signaling pathway(s) implicated in the control of melanocytic proliferation. Thus, we have generated a new mouse model for melanomagenesis. However, the molecular mechanisms that underlie these activities of RXR are not known. Given the importance of keratinocytes in regulating melanocyte mitogenesis, understanding how this regulation becomes aberrant in melanoma is significant, since it can possibly lead to the development of effective therapeutic strategies to counteract melanoma formation and progression. Our long-term goal is to identify the mechanisms of signal transduction between keratinocytes and melanocytes that contribute to the development of melanoma. Based on the above observations and from the preliminary data, we propose the following two specific aims. First, we propose to elucidate the cellular and molecular mechanisms by which keratinocytes control melanocyte mitogenesis and transformation leading to a malignant phenotype. Our working hypothesis is that RXRa, directly or indirectly, represses keratinocytic expression of endothelin 1 (ET-1), SCF, POMC and FGF2 which may serve to regulate melanocytic mitogenesis in a paracrine manner. Second, we propose to identify intracellular targets (melanocytic factors) that control melanocyte homeostasis and UV-induced melanomagenesis. Our working hypothesis is that melanocytic factors, such as cyclin dependent kinase-4 (Cdk4), may modulate the responsiveness of these cells to the mitogenic effects of keratinocyte-derived paracrine factors. We believe that our efforts in the context of the work described herein will lead to a detailed understanding of the mechanism(s) by which melanocyte mitogenesis and melanomagenesis are regulated by keratinocytic RXRa, and perhaps other paracrine factors. The proposed project is potentially innovative as our laboratory generated the RXRa [ep-/-] mouse that has been used for these studies, and was the first to characterize the in vivo role of RXRa in skin during epidermal homeostasis. This contribution is significant and the results are expected to have a positive impact on human health, because the outcome of the work will provide the molecular cornerstone for the development of future pharmacological strategies designed to treat, and ultimately cure malignant melanoma. PUBLIC HEALTH RELEVANCE: Melanoma is generally recognized as an aggressive skin cancer that can metastasize early in the course of the disease and is highly resistant to most current therapeutic interventions. Understanding the genetic and environmental factors driving melanoma formation is essential for the development of new therapies to treat this disease. The present study involves the use of a novel melanoma mouse model to study the molecular mechanism underlying the role of skin keratinocytes to control melanocyte mitogenesis and melanomagenesis.

描述（由申请人提供）：恶性黑色素瘤是美国增长最快的癌症之一，目前尚无有效的治疗方法。 太阳紫外线（UV）辐射，尤其是儿童时期的阳光照射是黑色素瘤的重要病因危险因素。 类维生素A X 受体a (RXRa) 是核受体(NR) 超家族的成员，是转导多种细胞信号的中心协调子。 在研究 RXRa 在皮肤中的作用的背景下，我们发现了这种 NR 在黑色素瘤生成中的一个意想不到的新颖作用：RXRa[ep-/-] 小鼠，特别是在表皮角质形成细胞中缺乏 RXRa，当接受两步化学致癌方案 (DMBA+TPA) 时，会高频率地出现类似于黑色素瘤的黑色素细胞生长 (MG)。 我们的结果表明 RXRa 可能调节角质形成细胞 ?黑素细胞信号通路涉及黑素细胞增殖的控制。 因此，我们建立了一种新的黑色素瘤发生小鼠模型。 然而，RXR 这些活性的分子机制尚不清楚。 鉴于角质形成细胞在调节黑色素细胞有丝分裂中的重要性，了解这种调节在黑色素瘤中如何变得异常具有重要意义，因为它可能导致开发有效的治疗策略来对抗黑色素瘤的形成和进展。 我们的长期目标是确定角质形成细胞和黑色素细胞之间促进黑色素瘤发展的信号转导机制。 根据上述观察和初步数据，我们提出以下两个具体目标。 首先，我们建议阐明角质形成细胞控制黑素细胞有丝分裂和转化导致恶性表型的细胞和分子机制。 我们的工作假设是，RXRa 直接或间接抑制内皮素 1 (ET-1)、SCF、POMC 和 FGF2 的角质形成细胞表达，这些表达可能以旁分泌方式调节黑素细胞有丝分裂发生。 其次，我们建议确定控制黑素细胞稳态和紫外线诱导的黑素瘤生成的细胞内靶标（黑素细胞因子）。 我们的工作假设是，黑素细胞因子，例如细胞周期蛋白依赖性激酶 4 (Cdk4)，可能调节这些细胞对角质形成细胞衍生的旁分泌因子的有丝分裂作用的反应。 我们相信，我们在本文描述的工作背景下的努力将导致对角化细胞 RXRa 以及可能还有其他旁分泌因子调节黑素细胞有丝分裂和黑素瘤生成的机制的详细了解。 拟议的项目具有潜在的创新性，因为我们的实验室生成了用于这些研究的 RXRa [ep-/-] 小鼠，并且是第一个表征表皮稳态期间 RXRa 在皮肤中的体内作用的小鼠。 这一贡献是重大的，研究结果预计将对人类健康产生积极影响，因为这项工作的成果将为开发未来旨在治疗并最终治愈恶性黑色素瘤的药理学策略提供分子基石。 公共卫生相关性：黑色素瘤通常被认为是一种侵袭性皮肤癌，可以在病程早期转移，并且对大多数当前的治疗干预措施具有高度抵抗力。 了解驱动黑色素瘤形成的遗传和环境因素对于开发治疗这种疾病的新疗法至关重要。 本研究涉及使用新型黑色素瘤小鼠模型来研究皮肤角质形成细胞控制黑色素细胞有丝分裂和黑色素瘤生成的分子机制。