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PMID: 8621239 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Decreased expression of nucleoside diphosphate kinase alpha isoform, an nm23-H2 gene homolog, is associated with metastatic potential of rat mammary-adenocarcinoma cells.

International journal of cancer ·Vol. 65 ·No. 4 ·1996-02-08 ·Pages 531-7

Fukuda M, Ishii A, Yasutomo Y, Shimada N, Ishikawa N, Hanai N, Nagata N, Irimura T, Nicolson GL, Kimura N

Abstract

The nm23 gene [encoding nucleoside diphosphate kinase (NDPK)] may act as a metastasis suppressor in certain tumor cells. We investigated the role of NDPK isoforms (alpha and beta) in the metastatic processes, using rat mammary-adenocarcinoma cell lines of poor (MTC) and high (MTLn3) spontaneous metastatic potential respectively. In these cell lines, as in most rat tissues, the alpha isoform (nm23-H2 homolog) was more highly expressed than the beta isoform (nm23-H1 homolog) at the mRNA and protein levels. When examined by Northern- and Western-blot analyses, expression of the 2 isoforms was reduced in highly metastatic MTLn3 cells compared with poorly metastatic MTC cells. The reduced expression was also associated with diminished NDPK-enzyme activity in the cell extracts. Southern-blot and RT-PCR-SSCP analyses suggested that the 2 genes were not grossly altered or mutated in their translation regions. MTLn3 cell clones transfected with NDPKalpha or NDPKbeta cDNA were all tumorigenic when implanted into the mammary fat pad of syngeneic rats. Among those, only clones transfected with the NDPKalpha gene exhibited reduced lung metastasis in a spontaneous metastasis assay.

MeSH Terms
Adenocarcinoma/enzymology,secondary Animals Base Sequence Female Isoenzymes/genetics,physiology Mammary Neoplasms, Experimental/enzymology,pathology Molecular Sequence Data Monomeric GTP-Binding Proteins NM23 Nucleoside Diphosphate Kinases Nucleoside-Diphosphate Kinase/genetics,physiology RNA, Messenger/analysis Rats Rats, Inbred F344 Transcription Factors/genetics,physiology Tumor Cells, Cultured
Chemicals
Isoenzymes NM23 Nucleoside Diphosphate Kinases RNA, Messenger Transcription Factors Nucleoside-Diphosphate Kinase Monomeric GTP-Binding Proteins
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Fukuda M
Department of Molecular Biology, Tokyo Metropolitan Institute of Gerontology, Japan.
Ishii A
Yasutomo Y
Shimada N
Ishikawa N
Hanai N
Nagata N
Irimura T
Nicolson G L
Kimura N
Article Info
Journal
International journal of cancer
Abbr.
Int J Cancer
ISSN
0020-7136
Published
1996-02-08
Pages
531-7
Language
English
Region
United States
NLM ID
0042124
Subset
IM
Grants
NCI NIH HHS · R01-CA63045 · United States
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