Understanding the role of metabolism in cancer
了解代谢在癌症中的作用
基本信息
- 批准号:10686279
- 负责人:
- 金额:$ 74.93万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2019
- 资助国家:美国
- 起止时间:2019-09-10 至 2026-08-31
- 项目状态:未结题
- 来源:
- 关键词:AffectBiochemicalBiochemistryBiomassCancer ModelCancer PatientCell Culture TechniquesCell ProliferationCellsCellular Metabolic ProcessDietDrug resistanceDrug usageEnvironmentEnvironmental Risk FactorEventGenerationsGeneticGoalsIntrinsic factorLaboratoriesMalignant NeoplasmsMass Spectrum AnalysisMetabolicMetabolic PathwayMetabolismModelingNormal CellNucleotidesNutrientNutrient availabilityPatientsPhysiologicalPhysiologyProductionProliferatingRegulationResearchRoleRunningSignal TransductionSupporting CellTechnologyTestingTissuesTrace Elements NutritionWorkcancer cellcancer geneticscancer therapycancer typeextracellulargenetic approachglucose metabolisminsightinterestmacromoleculemetabolic abnormality assessmentmetabolic phenotypemouse modelneoplastic cellnovelprogramstooltumortumor growthtumor initiationtumor metabolismtumor microenvironmenttumor progression
项目摘要
Project Summary
Cancer cells have metabolic requirements that differ from most normal, non-proliferating cells. To proliferate,
cancer cells must transform available nutrients into the varied array of macromolecules that are needed to
build a new cell. Each cancer type is unique and will run a metabolic program that depends on the tissue-of-
origin, genetic factors, and the local environment. How specific cancers integrate these cancer cell-intrinsic and
extrinsic factors to rewire metabolism and support cancer progression is a major unanswered question.
My laboratory's long-term goal is to understand how cancer cell metabolism is adapted to support tumor
initiation and progression. The metabolic phenotypes of proliferating cells are typically interpreted with an
emphasis on either energy generation or the crosstalk between signaling events and cell metabolism. This has
led many to focus on how cancer genetics influences metabolic pathway use. We take a different approach
that identifies limiting metabolic processes, considers how these are constrained by the extracellular
environment, and defines how metabolic limitations are overcome within a physiological tissue context.
Our work has provided insight into understanding how glucose metabolism affects cell proliferation. We found
that production of nucleotides and oxidized biomass can be metabolic limitations of cell proliferation and tumor
growth, and that both cancer cell-intrinsic and environmental factors determine how cells overcome these
limitations. We have developed novel tools to study metabolism in various physiological contexts and
uncovered metabolic differences between tumors and cancer cells in culture. We have demonstrated how
environmental nutrients and cancer lineage can dictate how metabolism is used to support proliferation and
determine sensitivity and resistance to drugs used in patients. Our work has charted new research directions
for the field and contributed new ideas to exploit altered metabolism to help cancer patients.
Using mass spectrometry to trace nutrient fate in cancer models, my laboratory generates hypotheses for how
different cancers use metabolism to support cell proliferation and tumor growth. We test these hypotheses
using a variety of biochemical and genetic approaches to define how nutrient availability, metabolic pathway
regulation, and tissue context constrain how cells use available materials to proliferate. Our current interests
include identifying which metabolic processes create bottlenecks for cell proliferation, determining how
metabolism is different in different cancers, examining in detail the influence of tissue type, tumor genetics, and
tumor microenvironment, and understanding how diet and whole body metabolism influence tumor metabolism
and cancer progression. We aim to advance understanding of metabolic pathway biochemistry, its relationship
to cancer and mammalian physiology, and identify how best to target metabolism for therapy.
项目总结
项目成果
期刊论文数量(3)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
A metabolic map of the DNA damage response identifies PRDX1 in the control of nuclear ROS scavenging and aspartate availability.
DNA损伤反应的代谢图可以确定核ROS清除和天冬氨酸可用性的PRDX1。
- DOI:10.15252/msb.202211267
- 发表时间:2023-07-11
- 期刊:
- 影响因子:9.9
- 作者:
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MATTHEW G. VANDER HEIDEN的其他文献
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{{ truncateString('MATTHEW G. VANDER HEIDEN', 18)}}的其他基金
Understanding the role of metabolism in cancer
了解新陈代谢在癌症中的作用
- 批准号:
10240613 - 财政年份:2019
- 资助金额:
$ 74.93万 - 项目类别:
Understanding the role of metabolism in cancer
了解新陈代谢在癌症中的作用
- 批准号:
10478159 - 财政年份:2019
- 资助金额:
$ 74.93万 - 项目类别:
Understanding the role of metabolism in cancer
了解新陈代谢在癌症中的作用
- 批准号:
10015240 - 财政年份:2019
- 资助金额:
$ 74.93万 - 项目类别:
Understanding the role of serine metabolism in cancer
了解丝氨酸代谢在癌症中的作用
- 批准号:
9098649 - 财政年份:2015
- 资助金额:
$ 74.93万 - 项目类别:
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:
8504354 - 财政年份:2013
- 资助金额:
$ 74.93万 - 项目类别:
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:
8625285 - 财政年份:2013
- 资助金额:
$ 74.93万 - 项目类别:
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 - 财政年份:2013
- 资助金额:
$ 74.93万 - 项目类别:
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:
9034555 - 财政年份:2013
- 资助金额:
$ 74.93万 - 项目类别:
Mouse Models to Evaluate the Role of Pyruvate Kinase Regulation in Cancer Biology
评估丙酮酸激酶调节在癌症生物学中的作用的小鼠模型
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7692920 - 财政年份:2008
- 资助金额:
$ 74.93万 - 项目类别:
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