Ribosomal Proteins Control Tumor Suppressor Pathways in Response to Nucleolar Stress

Bioessays. 2019 Mar;41(3):e1800183. doi: 10.1002/bies.201800183. Epub 2019 Feb 1.

Abstract

Ribosome biogenesis includes the making and processing of ribosomal RNAs, the biosynthesis of ribosomal proteins from their mRNAs in the cytosol and their transport to the nucleolus to assemble pre-ribosomal particles. Several stresses including cellular senescence reduce nucleolar rRNA synthesis and maturation increasing the availability of ribosome-free ribosomal proteins. Several ribosomal proteins can activate the p53 tumor suppressor pathway but cells without p53 can still arrest their proliferation in response to an imbalance between ribosomal proteins and mature rRNA production. Recent results on senescence-associated ribogenesis defects (SARD) show that the ribosomal protein S14 (RPS14 or uS11) can act as a CDK4/6 inhibitor linking ribosome biogenesis defects to the main engine of cell cycle progression. This work offers new insights into the regulation of the cell cycle and suggests novel avenues to design anticancer drugs.

Keywords: CDK4; RB; RPS14; cancer; ribosomal proteins; ribosome biogenesis; senescence.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cell Cycle / physiology
  • Cellular Senescence
  • Cyclin-Dependent Kinase 4 / metabolism
  • Cyclin-Dependent Kinase 6 / metabolism
  • Gene Expression
  • Humans
  • Mutation
  • Neoplasms / drug therapy
  • Neoplasms / genetics
  • Neoplasms / metabolism
  • RNA, Ribosomal / metabolism
  • Ribosomal Proteins / genetics*
  • Ribosomal Proteins / metabolism*
  • Ribosomes / metabolism
  • Signal Transduction / drug effects
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • RNA, Ribosomal
  • RPS14 protein, human
  • Ribosomal Proteins
  • TP53 protein, human
  • Tumor Suppressor Protein p53
  • CDK4 protein, human
  • CDK6 protein, human
  • Cyclin-Dependent Kinase 4
  • Cyclin-Dependent Kinase 6

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