Defining and targeting the epigenetic programs involved in melanoma development

定义和瞄准参与黑色素瘤发展的表观遗传程序

• 批准号: 10543558
• 负责人: Keiran Smalley
• 金额: $ 19.3万
• 依托单位: H. LEE MOFFITT CANCER CTR & RES INST
• 依托单位国家: 美国
• 财政年份: 2022
• 资助国家: 美国
• 起止时间: 2022-01-01 至 2024-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10543558
• 关键词: Ablation; Address; BRAF gene; Cell Death; Cell Line; Cell Survival; Cells; Cutaneous Melanoma; DNA Damage; Detection; Development; Ensure; Enzymes; Epigenetic Process; Gene Expression Profile; Genetic; Genetic Transcription; Grant; HDAC8 gene; Heterozygote; Immune; Immune Evasion; Immune system; Incidence; Individual; Lesion; Link; Malignant Neoplasms; Mediating; Melanoma Cell; Modeling; Mus; Mutation; Nature; Oncogenic; PTEN gene; Pathogenicity; Pathway interactions; Pharmaceutical Preparations; Prevention; Prevention strategy; Radiation induced damage; Reporting; Research; Research Proposals; Resistance; Role; Signal Transduction; Skin; Stress; T cell infiltration; Testing; UV Radiation Exposure; UV induced; UV-induced melanoma; Ultraviolet Rays; Work; cell injury; experience; immunogenicity; immunoregulation; in vivo; inhibitor; innovation; melanocyte; melanoma; mouse model; multiple omics; mutant; neoantigens; novel; prevent; programs; response; single-cell RNA sequencing; small molecule; sun damage; the sun; transcriptional reprogramming; tumor; tumor-immune system interactions; ultraviolet irradiation

Project summary Ultraviolet radiation (UVR) exposure has long been linked to melanoma development, with clear correlations seen between latitude and the incidence of melanoma, particularly in individuals with fair skin and a poor ability to tan. As such, sporadic cutaneous melanoma has one of the highest mutational burdens of all cancers. The high mutational burden following UVR exposure is associated with increased neoantigen load and greater immune recognition. These observations suggest that the melanocytes that initiate melanoma survive UVR - induced stress/cell damage and then avoid immune recognition. Unrelated studies in our lab focused on BRAF inhibitor resistance in melanoma identified a stress-activated epigenetic program mediated through histone deacetylase (HDAC)-8 that allowed escape from both cell death and immune recognition through transcriptional reprogramming. The objective of this proposal is to develop novel melanoma prevention strategies that target the epigenetic programs required for UVR-damaged melanocytes to avoid cell death and immune recognition. We will test the hypothesis that UVR-induced HDAC8 activation allows melanocytes to avoid cell death and immune attack, allowing cells with pathogenic mutations to survive and later develop into melanoma. This proposal is conceptually innovative in seeking to define the role of HDAC8 in the epigenetic reprogramming of melanocytes that experience UVR-induced stress and DNA damage. We will further address the role of immune evasion in the development of melanoma precursor lesions and will use unique mouse models, single cell RNA-Seq, and multi-Omics approaches to identify core pathways and regulators involved in the persistence of UVR-damaged melanocytes that constitute the precursor lesions for melanoma development. In Aim 1, we will define how HDAC8 modulates the transcriptional profile of melanocytes following UV-irradiation and will determine how this contributes to increased cell survival and reduced immunogenicity. We will then use our recently developed HDAC8 mouse model to demonstrate the role for HDAC8-induction in melanoma development and will perform single cell RNA-Seq and immune profiling to characterize how HDAC8 activation in melanocytes modulates the immune microenvironment of the skin. In Aim 2, we will determine whether inhibition of HDAC8 using genetic silencing or small molecule HDAC8 inhibitors reverses the survival and immune escape transcriptional programs that are activated in melanocytes following UVR exposure. In vivo studies will evaluate whether HDAC8 inhibitors or silencing of HDAC8 in mouse skin melanocytes are sufficient to delay the initiation of melanoma development in our BRAF mutant/PTEN-silenced melanoma model, and the role of the immune system in this response. At completion of this work we expect to have demonstrated the proof-of-principle for the development of HDAC8 inhibitors as a novel melanoma prevention strategy.

项目摘要 长期以来，紫外线辐射（UVR）暴露与黑色素瘤的发展有关，具有明显的相关性 在纬度和黑色素瘤的发病率之间，特别是在皮肤白皙和能力差的人中， 晒黑。因此，散发性皮肤黑色素瘤是所有癌症中突变负荷最高的癌症之一。的 UVR暴露后的高突变负荷与新抗原负荷增加相关， 免疫识别这些观察结果表明，引发黑色素瘤的黑色素细胞在紫外线照射下存活下来， 诱导应激/细胞损伤，然后避免免疫识别。我们实验室的非相关研究集中在BRAF 黑色素瘤中抑制剂抗性鉴定了通过组蛋白介导的应激激活的表观遗传程序 脱乙酰酶（HDAC）-8，允许逃避细胞死亡和免疫识别， 转录重编程这项提案的目的是开发新的黑色素瘤预防 针对紫外线损伤黑素细胞所需的表观遗传程序以避免细胞死亡的策略， 免疫识别我们将检验紫外线诱导的HDAC 8激活允许黑素细胞 避免细胞死亡和免疫攻击，使具有致病突变的细胞存活，然后发展成 黑素瘤该提议在寻求定义HDAC 8在表观遗传学中的作用方面具有概念创新性。 重编程的黑素细胞经历紫外线诱导的压力和DNA损伤。我们将进一步解决 免疫逃避在黑色素瘤前体病变发展中的作用，并将使用独特的小鼠 模型，单细胞RNA-Seq和多组学方法，以确定核心途径和参与调节 紫外线损伤的黑色素细胞持续存在，构成黑色素瘤的前驱病变 发展在目标1中，我们将定义HDAC 8如何调节黑素细胞的转录谱 并将确定这如何有助于增加细胞存活和减少 免疫原性然后，我们将使用我们最近开发的HDAC 8小鼠模型来证明 HDAC 8-诱导黑色素瘤的发展，并将进行单细胞RNA-Seq和免疫分析， 描述黑素细胞中HDAC 8的激活如何调节皮肤的免疫微环境。在 目的2，我们将确定是否使用基因沉默或小分子HDAC 8抑制HDAC 8 抑制剂逆转黑素细胞中激活的存活和免疫逃逸转录程序 紫外线照射后。体内研究将评估HDAC 8抑制剂或HDAC 8沉默是否在肿瘤中起作用。 小鼠皮肤黑素细胞足以延迟我们的BRAF中黑色素瘤发展的开始 突变/PTEN沉默的黑色素瘤模型，以及免疫系统在这种反应中的作用。完成时 这项工作，我们希望已经证明了HDAC 8抑制剂的发展作为一个原则的证明， 新的黑色素瘤预防策略。