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Molecular Pathways: Targeting MYC-induced Metabolic Reprogramming and Oncogenic Stress in Cancer

Overview
Journal Clin Cancer Res
Specialty Oncology
Date 2013 Jul 31
PMID 23897900
Citations 60
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Abstract

MYC is a multifunctional transcription factor that is deregulated in many human cancers. MYC impacts a collaborative genetic program that orchestrates cell proliferation, metabolism, and stress responses. Although the progression of MYC-amplified tumors shows robust dependence on MYC activity, directly targeting MYC as a therapeutic method has proven to be technically difficult. Therefore, alternative approaches are currently under development with a focus on interference with MYC-mediated downstream effects. To fuel rapid cell growth, MYC reprograms cancer cell metabolism in a way that is substantially different from normal cells. The MYC-induced metabolic signature is characterized by enhanced glucose and glutamine uptake, increased lactate production, and altered amino acid metabolism. Targeting MYC-reprogrammed cancer cell metabolism is considered to be promising based on multiple preclinical studies. In addition, the increased biosynthetic demand of MYC-driven tumors coupled with limited nutrient access within tumor microenvironments create multiple levels of oncogenic stress, which can also be used as tumor-specific targets for pharmacologic intervention. Presumably, the best therapeutic strategy for treating MYC-amplified tumors is combined targeting of multiple MYC-mediated pathways, especially those involved in regulating cell proliferation, metabolism, and oncogenic stress.

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References
1.
Qing G, Li B, Vu A, Skuli N, Walton Z, Liu X . ATF4 regulates MYC-mediated neuroblastoma cell death upon glutamine deprivation. Cancer Cell. 2012; 22(5):631-44. PMC: 3510660. DOI: 10.1016/j.ccr.2012.09.021. View

2.
AHLUWALIA G, Grem J, Hao Z, Cooney D . Metabolism and action of amino acid analog anti-cancer agents. Pharmacol Ther. 1990; 46(2):243-71. DOI: 10.1016/0163-7258(90)90094-i. View

3.
Vazquez A, Markert E, Oltvai Z . Serine biosynthesis with one carbon catabolism and the glycine cleavage system represents a novel pathway for ATP generation. PLoS One. 2011; 6(11):e25881. PMC: 3206798. DOI: 10.1371/journal.pone.0025881. View

4.
Ruggero D, Montanaro L, Ma L, Xu W, Londei P, Cordon-Cardo C . The translation factor eIF-4E promotes tumor formation and cooperates with c-Myc in lymphomagenesis. Nat Med. 2004; 10(5):484-6. DOI: 10.1038/nm1042. View

5.
Podar K, Anderson K . A therapeutic role for targeting c-Myc/Hif-1-dependent signaling pathways. Cell Cycle. 2010; 9(9):1722-8. PMC: 3155944. DOI: 10.4161/cc.9.9.11358. View