Cell Fate Control by Translation: mRNA Translation Initiation as a Therapeutic Target for Cancer Development and Stem

Hyun-Jung Kim1

  • 1Laboratory of Molecular Stem Cell Pharmacology, College of Pharmacy, Chung-Ang University, Seoul 156-756, Korea. hyunjungkim@cau.ac.kr.

Biomolecules
|November 2, 2019
PubMed

Insights

This review highlights how mRNA translation control, particularly initiation, impacts cancer and stem cell fate. Targeting key translation factors offers therapeutic potential for cancer treatment and stem cell regulation.

Area of Science:

  • Molecular Biology
  • Cell Biology
  • Biochemistry

Background:

  • Protein synthesis via mRNA translation is crucial for cell function and gene regulation.
  • Dysregulated translation contributes to cancer development through abnormal protein synthesis.
  • Protein synthesis machinery is vital for determining stem cell fate.

Purpose of the Study:

  • To review recent advances in understanding translational control, focusing on initiation.
  • To explore the role of translational control in cancer development and stem cell fate.
  • To discuss therapeutic targets and upstream signaling pathways affecting translation.

Main Methods:

  • Literature review of recent advances in translational control.
  • Analysis of therapeutic targets for cancer and stem cell regulation.
  • Introduction to upstream signaling pathways influencing translation initiation.

Main Results:

  • mRNA translation initiation is a key regulatory step in protein synthesis.
  • Specific translation factors (e.g., eIF4E, 4EBP, eIF2) are implicated in cancer and stem cell biology.
  • Upstream signaling pathways modulate translation initiation.

Conclusions:

  • Understanding translational control is essential for regulating protein expression.
  • Targeting mRNA translation offers promising strategies for cancer therapeutics.
  • Modulating translation is beneficial for stem cell fate regulation.

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