Roles of SIRT1 in normal hematopoietic and leukemic stem cells

SIRT1 在正常造血干细胞和白血病干细胞中的作用

• 批准号: 8109438
• 负责人: WENYONG CHEN
• 金额: $ 31.37万
• 依托单位: BECKMAN RESEARCH INSTITUTE/CITY OF HOPE
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-03-01 至 2016-02-29
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8109438
• 关键词: Address; Adult; Aging; Attenuated; Biological Assay; Blood; Bone Marrow Transplantation; CD34 gene; Cell Aging; Cell Survival; Cell physiology; Chromatin Structure; Chronic Myeloid Leukemia; Chronic-Phase Myeloid Leukemia; Cytogenetics; DNA Damage; DNA Repair; Data; Deacetylase; Development; Disease; Disease Progression; Epigenetic Process; Frequencies; G22P1 gene; Gene Expression; Gene Mutation; Gene Silencing; Genes; Genetic Recombination; Gleevec; Goals; Health; Hematopoietic Neoplasms; Hematopoietic stem cells; Human; Hypermethylation; Imatinib; Imatinib mesylate; In Vitro; Knock-out; Knowledge; Laboratories; Leukemic Hematopoietic Stem Cell; Longevity; Lower Organism; Maintenance; Malignant - descriptor; Malignant Neoplasms; Mammalian Cell; Mediating; Mission; Molecular; Mus; Mutagenesis; Mutation; Nonhomologous DNA End Joining; Outcome Study; Pathogenesis; Pathway interactions; Patients; Play; Protein p53; Proteins; Relapse; Research; Resistance; Role; Stem cells; Stream; Stress; Testing; Transplantation; Tumor Suppressor Proteins; Work; base; bcr-abl Fusion Proteins; biological adaptation to stress; cancer genetics; cancer prevention; cancer stem cell; cancer therapy; cell age; cell growth; cellular longevity; chemotherapy; design; disability; embryonic stem cell; fusion gene; improved; in vivo; inhibitor/antagonist; insight; knockout gene; leukemic stem cell; mouse model; normal aging; novel; novel strategies; novel therapeutics; promoter; reconstitution; resistance mechanism; response; small molecule; tumorigenesis

DESCRIPTION (provided by applicant): There is a fundamental gap in understanding molecular interrelationship between longevity and cancer. The long term goal is to understand how a stress-response gene SIRT1 is involved in regulating mammalian longevity and cancer, and to develop novel strategies for cancer treatment and prevention through modulating the gene. The objective of this application is to determine how SIRT1 regulates hematopoietic stem cell functions during aging and upon malignant transformation. The central hypothesis is that SIRT1 is essential for cellular longevity of normal hematopoietic stem cells during aging and under stress, and promotes survival of chronic myelogenous leukemia (CML) stem cells for chemoresistance. The rationale for the proposed research is that better understanding roles of SIRT1 normal and leukemic stem cells will help design an effective strategy to treat CML, and potentially other blood maligancies, by eradicating leukemic stem cells through modulating SIRT1. Thus, the proposed studies is relevant to the NIH's mission to develop fundamental knowledge that will potentially help to reduce the burdens of human disability. Guided by stong preliminary data, this hypothesis will be tested by pursuing three specific aims: 1) Determine the role of SIRT1 for normal hematopoietic stem cell functions; 2) Determine the role of SIRT1 for CML stem cell survival and chemoresistance; and 3) Determine how SIRT1 regulates mutagenesis in normal and leukemic stem cells. Under aim 1, the consequence of SIRT1 loss on hematopoietic stem cell frequency, quiescence and reconstitution capacity during aging and in response to DNA damage will be determined using bone marrow transplantation assay. Key SIRT1-mediated molecular pathways for stem cell functions will be deciphered. Under aim 2, CML stem cell survival upon inhibition of SIRT1, by gene knockout or small molecule inhibitor, will be determined. Under aim 3, the impact of SIRT1 loss or inhibition on developing genetic mutations in normal hematopoietic stem cells and CML stem cells will be investigated, and key SIRT1-regulated DNA damage repair pathways in stem cells will be identified. The proposed research is significant, because it is expected to shed insight on how SIRT1 plays a role in stem cell aging and tumorigenesis, and to develop a new strategy to eradicate resistant CML stem cells through modulating SIRT1 functions. PUBLIC HEALTH RELEVANCE: This proposal addresses mechanisms of resistance of chronic myelogenous leukemia stem cells to chemotherapy and aging of normal hematopoietic stem cells. The proposed studies have direct relevance to human health as they will shed important insight on how a mammalian stress-responsive gene SIRT1 may regulate cancer and aging. As an important translational outcome of these studies, the combination of SIRT1 inhibitors with BCR-ABL inhibitors may prove a novel therapeutic strategy to eradicate leukemia stem cells and improve treatment of chronic myelogenous leukemia.

描述（由申请人提供）：在理解长寿和癌症之间的分子相互关系方面存在根本性的差距。长期目标是了解应激反应基因SIRT 1如何参与调节哺乳动物的寿命和癌症，并通过调节该基因开发新的癌症治疗和预防策略。本申请的目的是确定SIRT 1在衰老和恶性转化过程中如何调节造血干细胞功能。核心假设是SIRT 1对于衰老和应激期间正常造血干细胞的细胞寿命至关重要，并促进慢性髓细胞性白血病（CML）干细胞的存活以获得化学抗性。这项研究的基本原理是，更好地了解SIRT 1正常和白血病干细胞的作用将有助于设计一种有效的策略来治疗CML，以及潜在的其他血液恶性肿瘤，通过调节SIRT 1来根除白血病干细胞。因此，拟议的研究与NIH的使命相关，即开发可能有助于减轻人类残疾负担的基础知识。在强有力的初步数据的指导下，这一假设将通过追求三个具体目标进行检验：1）确定SIRT 1对正常造血干细胞功能的作用; 2）确定SIRT 1对CML干细胞存活和化疗耐药性的作用; 3）确定SIRT 1如何调节正常和白血病干细胞的突变。在目标1下，将使用骨髓移植测定来确定SIRT 1损失对衰老期间和响应于DNA损伤的造血干细胞频率、静止和重建能力的影响。SIRT 1介导的干细胞功能的关键分子通路将被破译。在目标2下，将确定通过基因敲除或小分子抑制剂抑制SIRT 1后的CML干细胞存活率。在目标3下，将研究SIRT 1缺失或抑制对正常造血干细胞和CML干细胞中发生基因突变的影响，并确定干细胞中SIRT 1调控的关键DNA损伤修复途径。这项研究意义重大，因为它有望揭示SIRT 1如何在干细胞衰老和肿瘤发生中发挥作用，并开发出一种新的策略，通过调节SIRT 1功能来根除耐药CML干细胞。 公共卫生关系：该提案涉及慢性粒细胞白血病干细胞对化疗的抵抗机制和正常造血干细胞的衰老机制。这些研究与人类健康直接相关，因为它们将揭示哺乳动物应激反应基因SIRT 1如何调节癌症和衰老的重要见解。作为这些研究的一个重要转化结果，SIRT 1抑制剂与BCR-ABL抑制剂的组合可能被证明是一种根除白血病干细胞和改善慢性髓性白血病治疗的新治疗策略。