Investigation of aberrant translational control of c-myc in cell lines derived from patients with multiple myeloma

Curr Top Microbiol Immunol. 1997:224:269-76. doi: 10.1007/978-3-642-60801-8_28.

Abstract

In cell lines derived from patients with multiple myeloma (MM) we have found an elevation in the amount of the c-myc protein which is not accompanied by an increase in the level of mRNA or a change in the half-life of the protein. There is a 3.4 fold enhancement in the degree of association of the c-myc message with polysomes. This is not accompanied by an alteration in polysome size or a change in the transit time of the c-myc mRNA on the polysomes thus suggesting that there is in increase in the degree of mobilisation of the c-myc message. Sequencing of the c-myc 5'UTR has revealed the presence of a mutation in all the MM cell lines studied and we demonstrate that this mutation causes altered binding of cellular proteins to this RNA species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • DNA, Neoplasm / genetics
  • Genes, myc*
  • Humans
  • Multiple Myeloma / genetics*
  • Point Mutation
  • Protein Biosynthesis
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA, Neoplasm / genetics
  • RNA, Neoplasm / metabolism
  • Tumor Cells, Cultured

Substances

  • DNA, Neoplasm
  • RNA, Messenger
  • RNA, Neoplasm