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The Mechanisms of PKM2-Regulated Gene Expression in Tumor Development.

肿瘤发展中 PKM2 调节基因表达的机制。

基本信息

批准号：
8639502
负责人：
ZHIMIN LU
金额：
$ 32.2万
依托单位：
UNIVERSITY OF TX MD ANDERSON CAN CTR
依托单位国家：
美国
项目类别：
财政年份：
2013
资助国家：
美国
起止时间：
2013-04-01 至 2018-03-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8639502
关键词：
Acetylation Adenosine Triphosphate Binding Biological Markers Brain CD2 gene Cancer Patient Cell Cycle Progression Cell Nucleus Cell Proliferation Cells ChIP-seq Chromosome Segregation Chromosomes Cultured Tumor Cells Cyclin D1 DNA Data Development Differentiated Gene EGF gene Enzymes Epidermal Growth Factor Receptor Gene Expression Gene Expression Profile Genes Genetic Transcription Glioma Glycolysis Goals Growth and Development function Histone H3 Human Isoenzymes Kinetochores Lead Lysine Malignant Neoplasms Malignant neoplasm of lung Mediating Metabolism Microtubules Mitosis Molecular Profiling Mus Nature Nuclear Translocation Oxygen Phase Phase Transition Phosphorylation Phosphotransferases Play Production Prognostic Marker Promoter Regions Protein Isoforms Protein Kinase Proteins Public Health Publications Publishing Pyruvate Kinase Regulation Research Role S Phase Specimen Therapeutic Threonine Transactivation Tyrosine Warburg Effect aerobic glycolysis base c-myc Genes cancer cell cancer therapy cell growth clinically relevant clinically significant daughter cell genome wide association study glucose uptake histone acetyltransferase innovation migration neoplastic cell novel outcome forecast overexpression public health relevance tumor tumorigenesis

项目摘要

DESCRIPTION (provided by applicant): Pyruvate kinase isozyme type M2 (PKM2), which regulates the rate-limiting final step of glycolysis, is instrumental in tumorigenesis. In additionto its well-studied role in cell metabolism, PKM2 promotes cell proliferation though an unknown mechanism. Our recent published and preliminary data show that activation of EGFR results in PKM2 translocation into the nucleus, where PKM2 interacts with ¿-catenin and mediates ¿-catenin-transactivation. In addition, PKM2 phosphorylates histone H3 and Bub3, subsequently regulating gene transcription and cell mitosis, respectively. We hypothesize that PKM2 has an essential role in controlling gene expression and different phases of cell cycle progression, which is instrumental in EGFR activation-promoted tumor development. In Specific Aim 1, we will further elucidate the mechanisms underlying PKM2-mediated gene transcription and identify PKM2-regulated expression of genes in cancer cells by genome-wide screening. In Specific Aim 2, we will elucidate the mechanisms underlying PKM2-regulated chromosome segregation. In Specific Aim 3, we will determine the role of PKM2- regulated gene transcription and chromosome segregation in EGFR-promoted tumorigenesis. We expect that our proposed research will provide important and previously unrevealed mechanisms of EGFR-promoted tumor development via nonmetabolic functions of PKM2. Building on our findings, therapeutic strategies targeting PKM2-regulated gene expression may be developed to enhance current EGFR-based cancer therapies.

描述（由申请方提供）：丙酮酸激酶同工酶M2（PKM 2）调节糖酵解的限速最后步骤，在肿瘤发生中起作用。PKM 2除了在细胞代谢中的作用外，还通过一种未知的机制促进细胞增殖。我们最近发表的和初步的数据表明，EGFR的激活导致PKM 2易位到细胞核中，在那里PKM 2与<$-连环蛋白相互作用并介导<$-连环蛋白的反式激活。此外，PKM 2磷酸化组蛋白H3和Bub 3，随后分别调节基因转录和细胞有丝分裂。我们假设PKM 2在控制基因表达和细胞周期进展的不同阶段中起重要作用，这在EGFR激活促进肿瘤发展中起重要作用。在具体目标1中，我们将进一步阐明PKM 2介导的基因转录的机制，并通过全基因组筛选确定PKM 2调控的癌细胞基因表达。在具体目标2中，我们将阐明PKM 2调节染色体分离的机制。在具体目标3中，我们将确定PKM 2调节的基因转录和染色体分离在EGFR促进的肿瘤发生中的作用。我们希望我们提出的研究将通过PKM 2的非代谢功能提供EGFR促进肿瘤发展的重要和以前未揭示的机制。基于我们的研究结果，可以开发针对PKM 2调节基因表达的治疗策略，以增强目前基于EGFR的癌症治疗。