Eco-evolutionary drivers of clonal dynamics during UV-induced skin carcinogenesis (PQ3)

紫外线诱发皮肤癌过程中克隆动力学的生态进化驱动因素（PQ3）

• 批准号: 10379405
• 负责人: Joel Brown
• 金额: $ 62.72万
• 依托单位: H. LEE MOFFITT CANCER CTR & RES INST
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-04-01 至 2026-03-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10379405
• 关键词: Actinic keratosis; Architecture; Binding; Biological Models; Cancer Center; Carcinogens; Carcinoma; Cell division; Cells; Characteristics; Chronic; Clinical; Clonal Evolution; Development; Ecology; Environment; Epithelial; Event; Genetic; Genetic Transcription; Genomics; Goals; Heritability; Heterogeneity; Human; Human Cloning; Individual; Investigation; Lesion; Ligands; Link; Malignant - descriptor; Malignant Neoplasms; Mathematics; Measures; Mediating; Modeling; Molecular; Molecular Genetics; Mutation; Normal tissue morphology; Oncology; Pathogenicity; Phase; Proliferating; Running; Skin; Skin Cancer; Skin Carcinogenesis; Skin Carcinoma; Stress; Testing; Time; Tissues; Transplantation; UV Radiation Exposure; UV induced; Ultraviolet Rays; Variant; Work; cancer initiation; carcinogenesis; driver mutation; experience; fitness; in vivo; mathematical model; molecular dynamics; multidisciplinary; novel; premalignant; pressure; quantitative imaging; receptor; single cell sequencing; skin squamous cell carcinoma; trait; tumor; tumor microenvironment

ABSTRACT Cancers have readily-defined characteristics often referred to as “hallmarks”. Nevertheless, the question of how the sequence of cancer development progresses -- from normal tissue to carcinogen-damaged tissue to precancerous lesion and finally to malignant tumors – remains unanswered. Classically, these steps are attributed to the sequential acquisition of discrete genetic events such as driver mutations. However, in humans, the clonal dynamics governing cancer development happen over years, remain largely invisible even in model systems, and have been difficult to link to specific molecular changes. This rubric fails to account for clonal dynamics in the context of tissue architecture and fails to explain the consequences of large numbers of mutations present in normal tissue. Our long-term goal is to apply ecological and evolutionary principles to cancer initiation and development in order to test whether the hallmarks of cancer are acquired in three distinct phases each with distinct selective pressures and manifestations of cell competition and cooperation. Nowhere is this more accessible to investigation than in skin. For skin carcinomas, the most important carcinogen is ultraviolet radiation. Cutaneous squamous cell carcinoma (cuSCC) has the most tractable and clinically well-characterized progression sequence of any human cancer, from normal tissue, to a distinct precancerous lesion (the actinic keratosis), to invasive carcinoma. Therefore, it is ideal for establishing an eco- evolutionary paradigm of cancer initiation and development with respect to modelling clonal dynamics, genetic composition and the dynamics of molecular traits. Our central hypothesis is that cancer initiation and development occurs in three phases, each with specific and recognizable clonal dynamics. In the first phase, tissue disruption from UV exposure provides a permissive environment where extrinsically-driven mechanisms allow for some clones to experience unusually long runs of cell division and turnover. This greatly increases the variance among clone sizes with larger clones accumulating greater heritable variation. The second phase sees the emergence of intrinsic mechanisms where mutations that confer a competitive advantage allow for clonal selection with directed expansion of some clones at the expense of others. In the third phase, one or several clones escape local tissue control, acquire a distinct fitness function, and form tumors. Within the emerging tumor microenvironments, selection pressures will promote ecological and molecular diversification of the malignant clade (or clades). Our approach uses novel combinations of serial in-vivo quantitative imaging, mathematical modeling, and deep single-cell molecular interrogation to discern the ecological and molecular drivers of clonal dynamics, cell-to- cell competition and cooperation, and clonal evolution, producing a fundamentally unprecedented view of cancer initiation.

摘要 癌症具有容易定义的特征，通常被称为“标志”。然而， 癌症发展的顺序是如何发展的--从正常组织到致癌物损伤的组织， 癌前病变，最后是恶性肿瘤-仍然没有答案。传统上，这些步骤是 这归因于连续获得离散的遗传事件，如驱动突变。但在 人类，控制癌症发展的克隆动力学发生多年， 在模型系统中，很难将其与特定的分子变化联系起来。这个题目没有说明 克隆动态的背景下，组织结构，并未能解释的后果，大量的 突变存在于正常组织中。我们的长期目标是应用生态学和进化论的原则， 癌症的发生和发展，以测试癌症的标志是否是在三个 不同的阶段，每个阶段具有不同的选择压力和细胞竞争的表现， 合作 没有什么地方比皮肤更容易调查。对于皮肤癌，最重要的 致癌物质是紫外线辐射。皮肤鳞状细胞癌（cuSCC）具有最易处理， 任何人类癌症的临床上充分表征的进展序列，从正常组织到不同的组织， 癌前病变（光化性角化病），浸润性癌。因此，它是建立生态环境的理想选择， 癌症发生和发展的进化范式与克隆动力学模型，遗传 组成和分子性状的动态。 我们的中心假设是癌症的发生和发展分三个阶段，每个阶段都有特定的 和可识别的克隆动态。在第一阶段，来自UV暴露的组织破坏提供了允许的 外部驱动机制允许某些克隆经历异常长的 细胞分裂和周转。这大大增加了较大克隆大小之间的差异 积累更大的遗传变异。第二阶段是内在机制的出现 当赋予竞争优势的突变允许克隆选择时， 一些克隆人牺牲了另一些在第三阶段，一个或几个克隆逃脱了局部组织的控制， 获得一个独特的适应度函数，并形成肿瘤。在新出现的肿瘤微环境中， 压力将促进恶性分支（或多个分支）的生态和分子多样化。我们 该方法使用了一系列体内定量成像、数学建模和深度成像的新组合。 单细胞分子询问，以辨别克隆动力学的生态和分子驱动因素， 细胞竞争与合作，克隆进化，产生了一个前所未有的观点， 癌症起始。