Chromosomal localization and nucleoside diphosphate kinase-activity of human metastasis-suppressor genes NM23-1 and NM23-2 Journal Article


Authors: Backer, J. M.; Mendola, C. E.; Kovesdi, I.; Fairhurst, J. L.; O'Hara, B.; Eddy, R. L. Jr; Shows, T. B.; Mathew, S.; Murty, V. V. V. S.; Chaganti, R. S. K.
Article Title: Chromosomal localization and nucleoside diphosphate kinase-activity of human metastasis-suppressor genes NM23-1 and NM23-2
Abstract: Human metastasis-suppressor genes nm23-1 (NME1) and nm23-2 (NME2) are implicated in control of the metastatic potential of malignant cells. Using somatic cell hybrid analysis and fluorescence in situ hybridization we co-localized both genes to 17q21.3. The 17q21 region carries the locus responsible for early-onset familial breast-ovarian cancer and several other genes that are involved in tumorigenesis and differentiation and undergo frequent rearrangements during neoplastic development. Thus, our mapping places the NME genes in a region that may be subjected to multiple selection pressures. NME1 and NME2 genes were expressed as soluble proteins in a T7 bacterial expression system. Both proteins are independently active nucleoside diphosphate kinases and readily form intra- and intermolecular disulfide bonds. The biochemical properties of these proteins may explain the diversity of mature eucaryotic nucleoside diphosphate kinases.
Keywords: human genome; amplification; expression; identification; association; human breast-cancer; tumor-metastasis; insitu hybridization; binding-proteins; good prognosis
Journal Title: Oncogene
Volume: 8
Issue: 2
ISSN: 0950-9232
Publisher: Nature Publishing Group  
Date Published: 1993-02-01
Start Page: 497
End Page: 502
Language: English
ACCESSION: WOS:A1993KN00600030
PROVIDER: wos
PUBMED: 8381224
Notes: Note -- Source: Wos
Citation Impact
MSK Authors
  1. Raju S K Chaganti
    391 Chaganti
  2. Vundavalli V. V. S. Murty
    53 Murty
  3. Susan Mathew
    26 Mathew