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AKT2, a putative oncogene encoding a member of a subfamily of protein-serine/threonine kinases, is amplified in human ovarian carcinomas

  • Fox Chase Cancer Center

Research output: Contribution to journalArticlepeer-review

669 Scopus citations

Abstract

We isolated cDNA clones containing the entire coding region of the putative oncogene AKT2. Sequence analysis and in vitro translation demonstrated that AKT2 encodes a 56-kDa protein with homology to serine/threonine kinases; moreover, this protein contains a Src homology 2-like domain. AKT2 was shown to be amplified and overexpressed in 2 of 8 ovarian carcinoma cell lines and 2 of 15 primary ovarian tumors. AKT2 was mapped to chromosome region 19q13.1-q13.2 by fluorescence in situ hybridization. In the two ovarian carcinoma cell lines exhibiting amplification of AKT2, the amplified sequences were localized within homogeneously staining regions. We conclude that AKT2 belongs to a distinct subfamily of protein-serine/threonine kinases containing Src homology 2-like domains and that alterations of AKT2 may contribute to the pathogenesis of ovarian carcinomas.

Original languageEnglish
Pages (from-to)9267-9271
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume89
Issue number19
DOIs
StatePublished - Oct 1 1992

Keywords

  • Amino Acid Sequence
  • Chromosomes, Human/ultrastructure
  • Cloning, Molecular
  • DNA/genetics
  • Female
  • Fluorescent Dyes
  • Gene Amplification
  • Gene Library
  • Humans
  • Lymphocytes/cytology
  • Molecular Sequence Data
  • Multigene Family
  • Oncogene Proteins/genetics
  • Oncogenes
  • Ovarian Neoplasms/enzymology
  • Protein Biosynthesis
  • Protein Serine-Threonine Kinases/genetics
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-akt
  • Sequence Homology, Amino Acid
  • Transcription, Genetic

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