Structure and expression of the oncogene c-myc in fresh tumor material from patients with hematopoietic malignancies

Mol Cell Biol. 1984 Jun;4(6):1096-103. doi: 10.1128/mcb.4.6.1096-1103.1984.

Abstract

c-myc is the cellular gene homologous to the transforming sequence of MC29, an acute avian retrovirus. The human c-myc gene was cloned and used to study the structure and expression of c-myc in a variety of human hematopoietic malignancies. In a careful study of 106 patients, c-myc RNA was found to be expressed at elevated levels in tumor cells of 17 leukemia patients and five lymphoma patients. The c-myc gene was found to be rearranged in two lymphomas, an African Burkitt's lymphoma and a non-Hodgkins lymphoma in leukemic phase. The Burkitt's rearrangement involved the insertion of new DNA sequences upstream from the c-myc 5' coding region, presumably replacing the normal c-myc transcriptional promoter. None of the other 104 patients, including 20 with elevated myc expression, exhibited any evidence of a genetic rearrangement involving the c-myc gene. Our results show that there is a subset of hematopoietic malignancies characterized by elevated expression of c-myc. This elevated expression in most cases is not due to obvious genetic changes (rearrangement, amplification) at the c-myc locus nor to chromosomal translocations in the vicinity of this gene.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Base Sequence
  • Burkitt Lymphoma / genetics
  • Cloning, Molecular*
  • DNA Restriction Enzymes
  • Humans
  • Leukemia / genetics*
  • Lymphoma / genetics*
  • Nucleic Acid Hybridization
  • Oncogenes*
  • Reference Values

Substances

  • DNA Restriction Enzymes