The Role of BCL2 Mediated Calcium Signaling in Leukemia Stem Cell Metabolism

BCL2 介导的钙信号传导在白血病干细胞代谢中的作用

• 批准号: 10647882
• 负责人: Anagha Inguva
• 金额: $ 1.73万
• 依托单位: UNIVERSITY OF COLORADO DENVER
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-07-01 至 2023-10-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10647882
• 关键词: Acute Myelocytic Leukemia; Address; Affect; Animals; BCL2 gene; Biological Assay; Biological Models; Biology; Calcium; Calcium Channel; Calcium Channel Binding; Calcium Channel Inhibition; Calcium Signaling; Cell Death; Cell Survival; Cell physiology; Cellular Metabolic Process; Citric Acid Cycle; Compensation; Data; Dependence; Development; Disease; Disease Progression; Disease remission; Engraftment; Enzymes; Genetic; Genus Hippocampus; Hematologic Neoplasms; Hematopoietic stem cells; Homeostasis; Human; ITPR1 gene; Immune; Immunocompromised Host; Isocitrate Dehydrogenase; Jordan; Ketoglutarate Dehydrogenase Complex; Link; Maps; Mass Spectrum Analysis; Mediating; Membrane; Metabolic; Metabolism; Mitochondria; Molecular; Molecular Genetics; Movement; Mus; Outcome; Oxidative Phosphorylation; Pathway interactions; Patients; Pharmaceutical Preparations; Pharmacotherapy; Phosphorylation Inhibition; Population; Production; Proteins; Reaction; Regulation; Relapse; Resistance; Role; Sampling; Signal Transduction; Small Interfering RNA; Specimen; Structure-Activity Relationship; Testing; Therapeutic; Therapeutic Agents; Transplantation; Work; cancer stem cell; cell killing; cell type; chemotherapy; effective therapy; enzyme activity; experimental study; hematopoietic differentiation; improved; inhibitor therapy; knock-down; leukemic stem cell; metabolomics; mortality; novel; novel therapeutic intervention; novel therapeutics; overexpression; pharmacologic; pyruvate dehydrogenase; release of sequestered calcium ion into cytoplasm; response; self renewing cell; standard of care; stem cell biology; stem cell population; tool; uptake

PROJECT SUMMARY The objective of this study is to define the molecular mechanisms that control survival of malignant stem cells in acute myeloid leukemia (AML). Acute myeloid leukemia (AML) is a hematologic malignancy characterized by poorly differentiated hematopoietic stem cells (25). Traditionally, outcomes have been poor with a 30% response rate to standard of care in patients 65 years and older (25,26). A large cause of resistance and relapse to therapy is the persistence of leukemia stem cells (LSCs) (27-30). LSCs are a population of self-renewing cells that are able to initiate and maintain disease in immune-compromised animals (27). Traditional chemotherapy agents do not efficiently eradicate LSCs, and development of more effective therapies is a significant unmet need (27-30). Previous work from the Jordan lab has shown that LSCs have a unique dependence on oxidative phosphorylation (OXPHOS) for energy production (1-3,24). Further, BCL2 has a non-canonical role in regulating LSC metabolism as inhibition of BCL2 led to decreased OXPHOS and subsequent cell death in primary human LSCs (1-3,24). Analysis of samples from AML patients treated with the BCL2 inhibitor drug venetoclax revealed direct targeting of LSCs, which correlated with a 70% response rate (3). Thus, the underlying premise of the current proposal is that BCL2-mediated control of OXPHOS represents a key vulnerability that can be exploited to selectively target LSCs. Further, determining how OXPHOS is inhibited through BCL2 has implications for improving therapeutic strategies for AML patients. This proposal aims to elucidate the mechanistic link between BCL2 and LSC OXPHOS. In several model systems, BCL2 has been shown to have a non-canonical function in influencing calcium uptake and release at the ER and mitochondria through direct interactions with membrane bound calcium channels (7). Intracellular calcium homeostasis is crucial for cell survival, signaling and metabolism. In particular, the three rate limiting enzymes of the TCA cycle, pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase and isocitrate dehydrogenase are calcium dependent reactions (7). Therefore, BCL2 mediated calcium movement between the ER and mitochondria could be a mechanistic link between BCL2 and OXPHOS activity. BCL2 modulates the activity of calcium channels at the ER and mitochondria differently, based on the cell type being studied (7). Therefore, my proposal is focused on determining how BCL2 modulates OXPHOS activity by regulating calcium channel biology in leukemia stem cells. My hypothesis is that BCL2 mediated calcium localization is a critical regulator of OXPHOS activity in leukemia stem cells. This proposal will determine whether 1) BCL2 mediates calcium channel biology in LSCs 2) calcium channel biology modulates LSC metabolism/function and 3) regulation of calcium localization is the mechanism of action of BCL2 inhibition in LSCs.

项目摘要 本研究的目的是确定控制恶性肿瘤干细胞存活的分子机制， 急性髓细胞白血病（AML）急性髓性白血病（AML）是一种血液恶性肿瘤， 低分化造血干细胞（25）。传统上，结果一直很差， 65岁及以上患者对标准治疗的应答率（25，26）。耐药和复发的一大原因 白血病干细胞（LSC）的持续存在（27-30）。LSC是一群自我更新的细胞 能够在免疫受损的动物中引发和维持疾病（27）。传统化疗 药物不能有效地根除LSC，并且开发更有效的疗法是一个重大的未满足的问题。 需要（27-30）。 约旦实验室以前的工作表明，LSC对氧化应激有独特的依赖性。 磷酸化（OXPHOS）用于能量产生（1- 3，24）。此外，BCL 2在调节细胞凋亡中具有非经典作用。 LSC代谢作为BCL 2的抑制导致原代人中OXPHOS减少和随后的细胞死亡 LSC（1- 3，24）。对接受BCL 2抑制剂药物维奈托克治疗的AML患者的样本进行分析， 直接靶向LSC，与70%的应答率相关（3）。因此， 目前的建议是，BCL 2介导的OXPHOS控制代表了一个关键的漏洞，可以利用 选择性地瞄准LSC。此外，确定OXPHOS如何通过BCL 2被抑制具有以下意义： 改善AML患者的治疗策略。 该提案旨在阐明BCL 2和LSC OXPHOS之间的机制联系。在几个模型中， 在系统中，BCL 2已被证明在影响钙的吸收和释放方面具有非经典功能。 ER和线粒体通过与膜结合钙通道的直接相互作用（7）。细胞内 钙稳态对于细胞存活、信号传导和代谢至关重要。特别是，三个速率限制 TCA循环的酶、丙酮酸脱氢酶、α-酮戊二酸脱氢酶和异柠檬酸 脱氢酶是钙依赖性反应（7）。因此，BCL 2介导的钙离子在 ER和线粒体可能是BCL 2和OXPHOS活性之间机械联系。BCL 2调节 根据所研究的细胞类型，ER和线粒体上钙通道的活性不同（7）。 因此，我的建议集中在确定BCL 2如何通过调节钙来调节OXPHOS活性 白血病干细胞中的通道生物学。我的假设是，BCL 2介导的钙定位是一种 白血病干细胞中OXPHOS活性的关键调节因子。该提案将确定1）BCL 2 2）钙通道生物学调节LSC代谢/功能， 3)钙定位的调节是BCL 2抑制在LSC中的作用机制。