LEF/TCF Function in Adult Stem Cell Fate and Tumorigenesis

LEF/TCF 在成体干细胞命运和肿瘤发生中的功能

• 批准号: 7272718
• 负责人: STEPHEN R LYLE
• 金额: $ 27.58万
• 依托单位: UNIV OF MASSACHUSETTS MED SCH WORCESTER
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-08-08 至 2011-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7272718
• 关键词: Adult; Affect; Binding; Binding Sites; Biochemical; Cancer Biology; Cell Adhesion; Cell Line; Cell physiology; Cells; Characteristics; Code; Colon; Colon Carcinoma; Commit; Cutaneous; DNA Repair; DNA Sequence; Defect; Development; Dominant-Negative Mutation; Endometrial Carcinoma; Epithelial; Erinaceidae; Excision; Exons; Eye; Eyelid structure; Family; Frameshift Mutation; Gene Targeting; Genes; Genetic Transcription; Genomics; Genus Cola; Goals; Growth; Histopathologic Grade; Homeostasis; Human; Immunophenotyping; In Vitro; Incidence; Individual; Inherited; Lead; Malignant - descriptor; Malignant Epithelial Cell; Malignant Neoplasms; Mediating; Methods; Microsatellite Instability; Microsatellite Repeats; Mismatch Repair; Molecular; Morphology; Mus; Mutation; Mutation Analysis; Neoplasms; Nuclear; Oncogenic; Pathogenesis; Pathway interactions; Patients; Play; Property; Regulation; Relative (related person); Research Personnel; Risk; Role; Sampling; Sebaceous Adenocarcinoma; Sebaceous Gland Neoplasms; Signal Transduction; Skin; Skin Neoplasms; Stem cells; Surveys; Syndrome; System; TCF Transcription Factor; TCF7L2 gene; Techniques; Testing; Tissue Banks; Tissues; Transcriptional Activation; Transgenic Mice; Up-Regulation; Work; adult stem cell; carcinogenesis; cell growth; human stem cells; in vitro Assay; insight; malignant phenotype; neoplastic cell; novel; prevent; smoothened signaling pathway; stem cell fate; transcription factor; tumor; tumorigenesis

DESCRIPTION (provided by applicant): The long-term objectives of this proposal are to understand how specific genetic changes cause abnormal fate determination and growth regulation within adult epithelial stem cells and how these changes promote tumor formation from stem cells. The LEF/TCF family of transcription factors play an essential role in stem cell-mediated skin homeostasis. We have shown that human sebaceous tumors are similar to mouse tumors induced by a dominant negative Lef-1 gene and we recently identified mutations within the LEF-1 gene of sebaceous skin tumors. In addition, TCF-4 mutations occur in a significant proportion of colon cancers. Thus, our HYPOTHESIS is that LEF/TCF mutations cause abnormal stem cell fate determination and growth that promotes the formation of sebaceous tumors of the skin. Specific Aims: (1) Determine the cellular mechanisms by which dysregulated LEF-1 promotes tumorigenesis in multi-potent stem cells of human skin. (2) Determine the cellular and molecular properties of a new sebaceous tumor cell line showing deficient LEF-1 signaling. (3) Survey the spectrum and incidence of LEF/TCF mutations in human sebaceous skin tumors and correlate with tumor morphology. In order to accomplish these aims, we will use a novel system to isolate adult epithelial stem cells of human skin and study the cellular changes induced by altered LEF-1 signaling. We will use in vitro assays, as well as molecular and biochemical tests to characterize a new sebaceous tumor cell line. Lastly, a large archival tissue bank of sebaceous tumors will be screened by several molecular techniques to identify mutations within the LEF-1, TCF-3 and TCF-4 genes. Relevance: Patients with Muir-Torre syndrome, a genetically inherited defect of DNA repair, develop many sebaceous skin tumors and are at a high risk of colon cancer. Sebaceous tumors of the eyelid require removal of the eye in almost 25% of patients. This work should provide significant insights into the pathogenesis of sebaceous skin tumors, may lead to new ways of preventing or treating these tumors and may have broader implications for other cancers arising from adult epithelial stem cells.

描述（由申请人提供）：本提案的长期目标是了解特定遗传变化如何导致成体上皮干细胞内的异常命运决定和生长调节，以及这些变化如何促进干细胞形成肿瘤。LEF/TCF转录因子家族在干细胞介导的皮肤稳态中起重要作用。我们已经表明，人类皮脂腺肿瘤是类似于小鼠肿瘤诱导的显性负LEF-1基因，我们最近确定的突变LEF-1基因的皮脂腺皮肤肿瘤。此外，TCF-4突变发生在结肠癌的显著比例中。因此，我们的假设是LEF/TCF突变导致异常的干细胞命运决定和生长，促进皮肤皮脂腺肿瘤的形成。具体目的：（1）确定LEF-1失调促进人皮肤多能干细胞肿瘤发生的细胞机制。(2)确定一种新的显示LEF-1信号传导缺陷的皮脂腺肿瘤细胞系的细胞和分子特性。(3)调查人类皮脂腺皮肤肿瘤中LEF/TCF突变的谱和发生率，并与肿瘤形态学相关。为了实现这些目标，我们将使用一种新的系统来分离人皮肤的成体上皮干细胞，并研究由改变的LEF-1信号转导诱导的细胞变化。我们将使用体外分析，以及分子和生化测试，以表征一个新的皮脂腺肿瘤细胞系。最后，将通过多种分子技术筛选大型皮脂腺肿瘤档案组织库，以识别LEF-1、TCF-3和TCF-4基因内的突变。相关性：Muir-Torre综合征是一种遗传性DNA修复缺陷，患者会发生许多皮脂腺皮肤肿瘤，患结肠癌的风险很高。几乎25%的眼睑皮脂腺肿瘤患者需要切除眼睛。这项工作将为皮脂腺皮肤肿瘤的发病机制提供重要的见解，可能会导致预防或治疗这些肿瘤的新方法，并可能对成人上皮干细胞引起的其他癌症产生更广泛的影响。