Hypoxia induces differential translation of enolase/MBP-1

BMC Cancer. 2010 Apr 22:10:157. doi: 10.1186/1471-2407-10-157.

Abstract

Background: Hypoxic microenvironments in tumors contribute to transformation, which may alter metabolism, growth, and therapeutic responsiveness. The alpha-enolase gene encodes both a glycolytic enzyme (alpha-enolase) and a DNA-binding tumor suppressor protein, c-myc binding protein (MBP-1). These divergent alpha-enolase gene products play central roles in glucose metabolism and growth regulation and their differential regulation may be critical for tumor adaptation to hypoxia. We have previously shown that MBP-1 and its binding to the c-myc P2 promoter regulates the metabolic and cellular growth changes that occur in response to altered exogenous glucose concentrations.

Results: To examine the regulation of alpha-enolase and MBP-1 by a hypoxic microenvironment in breast cancer, MCF-7 cells were grown in low, physiologic, or high glucose under 1% oxygen. Our results demonstrate that adaptation to hypoxia involves attenuation of MBP-1 translation and loss of MBP-1-mediated regulation of c-myc transcription, evidenced by decreased MBP-1 binding to the c-myc P2 promoter. This allows for a robust increase in c-myc expression, "early c-myc response", which stimulates aerobic glycolysis resulting in tumor acclimation to oxidative stress. Increased alpha-enolase mRNA and preferential translation/post-translational modification may also allow for acclimatization to low oxygen, particularly under low glucose concentrations.

Conclusions: These results demonstrate that malignant cells adapt to hypoxia by modulating alpha-enolase/MBP-1 levels and suggest a mechanism for tumor cell induction of the hyperglycolytic state. This important "feedback" mechanism may help transformed cells to escape the apoptotic cascade, allowing for survival during limited glucose and oxygen availability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast Neoplasms / enzymology
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • Cell Cycle / genetics
  • Cell Growth Processes / genetics
  • Cell Hypoxia / genetics*
  • Cell Line, Tumor
  • DNA-Binding Proteins / biosynthesis
  • DNA-Binding Proteins / genetics*
  • Excitatory Amino Acid Transporter 2 / metabolism
  • Gene Expression Regulation, Neoplastic
  • Glucose / metabolism
  • Humans
  • Lactic Acid / biosynthesis
  • Phosphopyruvate Hydratase / biosynthesis
  • Phosphopyruvate Hydratase / genetics*
  • Phosphorylation
  • Promoter Regions, Genetic
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reactive Oxygen Species / metabolism
  • Translocation, Genetic
  • Up-Regulation

Substances

  • DENND4A protein, human
  • DNA-Binding Proteins
  • Excitatory Amino Acid Transporter 2
  • RNA, Messenger
  • Reactive Oxygen Species
  • Lactic Acid
  • Phosphopyruvate Hydratase
  • Glucose