Regulation of glucose metabolism to allow tumor initiation and growth

调节葡萄糖代谢以允许肿瘤发生和生长

• 批准号: 8827286
• 负责人: MATTHEW G. VANDER HEIDEN
• 金额: $ 30万
• 依托单位: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-04-01 至 2016-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8827286
• 关键词: ATP Synthesis Pathway; Alleles; Animal Model; Biochemical; Biochemistry; Biomass; Cancer Model; Cell Proliferation; Cells; Cellular Stress; Characteristics; Cultured Cells; Enzyme Activation; Enzymes; Exons; Genetically Engineered Mouse; Glucose; Goals; Growth; Health; Human; In Vitro; Lead; Maintenance; Malignant Neoplasms; Messenger RNA; Metabolic; Metabolic Pathway; Metabolic stress; Metabolism; Mus; Normal Cell; Normal tissue morphology; Nutrient; Patients; Play; Process; Property; Protein Isoforms; Proteins; Pyruvate; Pyruvate Kinase; RNA Splicing; Regulation; Rest; Role; Signal Transduction; Staging; Supporting Cell; Techniques; Technology; Testing; Tissues; Tumor Biology; Warburg Effect; Work; aerobic glycolysis; base; cancer cell; cancer initiation; cancer therapy; cell growth; enzyme activity; experience; glucose metabolism; glucose uptake; human cancer mouse model; human tissue; implantation; improved; in vivo; insight; meetings; mouse model; neoplastic cell; programs; rapid growth; research study; response; small molecule; success; tumor; tumor growth; tumor initiation; tumor metabolism; tumor progression; tumorigenesis

DESCRIPTION (provided by applicant): Altered glucose metabolism is a characteristic feature of most cancer cells, yet it is still poorly understood. Because altered metabolism represents a fundamental difference that exists between cancer cells and normal cells, targeting metabolism holds great promise for improved cancer therapy. However, success depends on understanding how metabolic regulation provides an advantage for tumor cells in relevant cancer models. Cancer cells require altered metabolism to efficiently incorporate nutrients such as glucose into biomass to support proliferation. Our understanding of how cancer cells meet these metabolic needs is based primarily on studies of cultured cells, and nutrient levels in vitro are significanty different from those experienced by tumor cells in vivo. Furthermore, cell proliferation rates in tumors can be low, particularly under conditions of metabolic stress, and a separate metabolic program from that used to support proliferation is needed for cells to thrive when nutrients are limited. Our long-term objective is to develop a comprehensive understanding of how cell metabolism is altered to support all stages of cancer progression in vivo. The M2 isoform of pyruvate kinase (PKM2) promotes glucose use for anabolic processes and is the pyruvate kinase isoform found in all human tumors described to date. The PKM1 isoform is found in many differentiated tissues and promotes efficient ATP synthesis from available nutrients. Paradoxically, despite increased glucose metabolism in cancers, PKM2 expression is associated with decreased pyruvate kinase enzyme activity, and complete loss of PKM2 can accelerate tumor growth. We aim to use genetically engineered mouse cancer models and small molecule pyruvate kinase activators in combination with biochemical approaches to understand how pyruvate kinase regulates glucose metabolism in tumors. We also aim to understand how this regulation contributes to cancer initiation and progression and any non-glycolytic PKM2 functions that might be important for tumors. In Specific Aim 1, we will take advantage of mice with conditional pyruvate kinase alleles to define the role of PKM1 and PKM2 in tumor initiation, as well as determine how pyruvate kinase isoform expression influences the growth of established tumors. In Specific Aim 2, we will investigate how the different regulatory properties of PKM2 influence glucose metabolism and how this impacts tumor biology. In Specific Aim 3, we will determine how cells continue to metabolize glucose in the absence of pyruvate kinase. Together, these studies will advance our understanding of glycolytic regulation in cancer cells in vivo. They will also inform how best to target glucose metabolism for improved cancer therapy.

描述（申请人提供）：葡萄糖代谢改变是大多数癌细胞的特征，但对其了解甚少。因为代谢的改变代表了癌细胞和正常细胞之间存在的根本差异，靶向代谢对改善癌症治疗有很大的希望。然而，成功取决于理解代谢调节如何在相关癌症模型中为肿瘤细胞提供优势。癌细胞需要改变新陈代谢，以有效地将葡萄糖等营养物质纳入生物量，以支持增殖。我们对癌细胞如何满足这些代谢需求的理解主要是基于对培养细胞的研究，体外的营养水平与肿瘤细胞在体内的营养水平有很大不同。此外，肿瘤中的细胞增殖率可能很低，特别是在代谢应激的条件下，当营养物质有限时，细胞需要一个独立的代谢程序来支持增殖。我们的长期目标是全面了解细胞代谢是如何改变的，以支持体内所有阶段的癌症进展。丙酮酸激酶（PKM2）的M2异构体促进葡萄糖用于合成代谢过程，是迄今为止在所有人类肿瘤中发现的丙酮酸激酶异构体。PKM1异构体存在于许多分化的组织中，并促进有效的ATP合成。矛盾的是，尽管癌症中葡萄糖代谢增加，PKM2的表达与丙酮酸激酶活性降低有关，PKM2的完全丧失可以加速肿瘤的生长。我们的目标是利用基因工程小鼠癌症模型和小分子丙酮酸激酶激活剂结合生化方法来了解丙酮酸激酶如何调节肿瘤中的葡萄糖代谢。我们还旨在了解这种调节如何促进癌症的发生和进展，以及PKM2可能对肿瘤很重要的任何非糖酵解功能。在Specific Aim 1中，我们将利用具有条件丙酮酸激酶等位基因的小鼠来确定PKM1和PKM2在肿瘤起始中的作用，并确定丙酮酸激酶异构体表达如何影响已建立肿瘤的生长。在Specific Aim 2中，我们将研究PKM2的不同调控特性如何影响葡萄糖代谢以及这如何影响肿瘤生物学。在特异性目标3中，我们将确定在丙酮酸激酶缺失的情况下细胞如何继续代谢葡萄糖。总之，这些研究将促进我们对癌细胞体内糖酵解调节的理解。他们还将告知如何最好地针对葡萄糖代谢来改善癌症治疗。