MCT1-mediated transport of a toxic molecule is an effective strategy for targeting glycolytic tumors.
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How drugs get into cells: tested and testable predictions to help discriminate between transporter-mediated uptake and lipoidal bilayer diffusionNovel drugs that target the metabolic reprogramming in renal cell cancerLactate Contribution to the Tumor Microenvironment: Mechanisms, Effects on Immune Cells and Therapeutic RelevanceStarved and Asphyxiated: How Can CD8(+) T Cells within a Tumor Microenvironment Prevent Tumor ProgressionGenome Editing Using Mammalian Haploid CellsGlutamine and cancer: cell biology, physiology, and clinical opportunitiesHow does the metabolism of tumour cells differ from that of normal cellsGenome wide functional genetics in haploid cellsHeterogeneity of glycolysis in cancers and therapeutic opportunities.The HK2 Dependent "Warburg Effect" and Mitochondrial Oxidative Phosphorylation in Cancer: Targets for Effective Therapy with 3-BromopyruvateHunting Viral Receptors Using Haploid CellsHuman Haploid Cell Genetics Reveals Roles for Lipid Metabolism Genes in Nonapoptotic Cell DeathHaploid genetic screens identify an essential role for PLP2 in the downregulation of novel plasma membrane targets by viral E3 ubiquitin ligasesDynamic and influential interaction of cancer cells with normal epithelial cells in 3D culture.Functional toxicology: tools to advance the future of toxicity testing.Targeting MYC Dependence by Metabolic Inhibitors in CancerRadiosynthesis and validation of (±)-[18F]-3-fluoro-2-hydroxypropionate ([18F]-FLac) as a PET tracer of lactate to monitor MCT1-dependent lactate uptake in tumorsInhibition of ATPIF1 ameliorates severe mitochondrial respiratory chain dysfunction in mammalian cells.Inhibition of glucose turnover by 3-bromopyruvate counteracts pancreatic cancer stem cell features and sensitizes cells to gemcitabine.Tumor bioenergetics: an emerging avenue for cancer metabolism targeted therapyThe basal epithelial marker P-cadherin associates with breast cancer cell populations harboring a glycolytic and acid-resistant phenotype.Metabolic determinants of cancer cell sensitivity to glucose limitation and biguanides.Megabase-scale deletion using CRISPR/Cas9 to generate a fully haploid human cell line.3-bromopyruvate enhanced daunorubicin-induced cytotoxicity involved in monocarboxylate transporter 1 in breast cancer cellsTumor metabolism, cancer cell transporters, and microenvironmental resistance.The adaptor protein p66Shc inhibits mTOR-dependent anabolic metabolism.Systemic administration of 3-bromopyruvate reveals its interaction with serum proteins in a rat model.Catabolism of exogenous lactate reveals it as a legitimate metabolic substrate in breast cancer.Metabolic regulation of cancer cell side population by glucose through activation of the Akt pathway.The energy blocker inside the power house: Mitochondria targeted delivery of 3-bromopyruvate.Cancer metabolism: strategic diversion from targeting cancer drivers to targeting cancer suppliersGene transfer and genome-wide insertional mutagenesis by retroviral transduction in fish stem cells.Molecular Pathways: Targeting Cellular Energy Metabolism in Cancer via Inhibition of SLC2A1 and LDHAFunctional genomic screening approaches in mechanistic toxicology and potential future applications of CRISPR-Cas9.3-BrPA eliminates human bladder cancer cells with highly oncogenic signatures via engagement of specific death programs and perturbation of multiple signaling and metabolic determinants.Identification of Genes That Modulate Susceptibility to Formaldehyde and Imatinib by Functional Genomic Screening in Human Haploid KBM7 Cells.Hypoxic resistance of KRAS mutant tumor cells to 3-Bromopyruvate is counteracted by Prima-1 and reversed by N-acetylcysteine.Merkel Cell Polyomavirus Small T Antigen Promotes Pro-Glycolytic Metabolic Perturbations Required for Transformation.Primary clear cell renal carcinoma cells display minimal mitochondrial respiratory capacity resulting in pronounced sensitivity to glycolytic inhibition by 3-BromopyruvateTargeting glucose metabolism in cancer: new class of agents for loco-regional and systemic therapy of liver cancer and beyond?
P2860
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P2860
MCT1-mediated transport of a toxic molecule is an effective strategy for targeting glycolytic tumors.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
MCT1-mediated transport of a t ...... r targeting glycolytic tumors.
@ast
MCT1-mediated transport of a t ...... r targeting glycolytic tumors.
@en
type
label
MCT1-mediated transport of a t ...... r targeting glycolytic tumors.
@ast
MCT1-mediated transport of a t ...... r targeting glycolytic tumors.
@en
prefLabel
MCT1-mediated transport of a t ...... r targeting glycolytic tumors.
@ast
MCT1-mediated transport of a t ...... r targeting glycolytic tumors.
@en
P2093
P2860
P50
P356
P1433
P1476
MCT1-mediated transport of a t ...... r targeting glycolytic tumors.
@en
P2093
Amanda W Hutchins
Catherine E Koch
Clary B Clish
David M Sabatini
Kivanç Birsoy
Omer H Yilmaz
Thijn R Brummelkamp
Tim R Peterson
Yetis Gultekin
P2860
P2888
P304
P356
10.1038/NG.2471
P407
P577
2012-12-02T00:00:00Z
P5875
P6179
1053270214