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PMID: 7907945 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Expression of metastasis-related nm23-H1 and nm23-H2 genes in ovarian carcinomas: correlation with clinicopathology, EGFR, c-erbB-2, and c-erbB-3 genes, and sex steroid receptor expression.

Cancer research ·Vol. 54 ·No. 7 ·1994-04-01 ·Pages 1825-30

Mandai M, Konishi I, Koshiyama M, Mori T, Arao S, Tashiro H, Okamura H, Nomura H, Hiai H, Fukumoto M

Abstract

To verity the role of metastasis-related nm23 genes in carcinogenesis and progression of ovarian carcinoma, we analyzed the mRNA levels of the nm23 genes of both isoforms, -H1 and -H2, together with those of the epidermal growth factor receptor, the c-erbB-2, and the c-erbB-3 genes in 45 ovarian carcinomas and 5 benign cystadenomas. Expressions of nm23 gene products/nucleoside diphosphate kinases, epidermal growth factor receptor, erbB-2 protein, and sex steroid receptor status in ovarian carcinomas were also examined by immunohistochemistry. The mRNA levels of nm23-H1 and nm23-H2 were higher in carcinoma tissues compared with benign tumors (H1, P < 0.01). The mRNA levels of c-erbB-2 and c-erbB-3 were also elevated in carcinoma tissues, and there was a positive correlation between mRNA levels of the nm23-H1 and the c-erbB-2 genes (r = 0.58; P < 0.05). Correlation of immunohistochemical staining between nucleoside diphosphate kinases and erbB-2 protein was also observed in ovarian carcinoma tissues. Sex steroid receptor positivity was related to a higher expression of nucleoside diphosphate kinases. Expression levels of the nm23 genes in ovarian carcinomas were not related to either histological subtype or local extension and peritoneal dissemination. Among stage III ovarian carcinomas, however, tumors possessing lymph node metastasis showed significantly lower nm23-H1 mRNA levels than those without nodal involvement (P < 0.05). Stage IV carcinomas also exhibited lower nm23-H1 and nm23-H2 expression levels compared with other stages (P < 0.05). These results suggest that expression of the nm23 genes, especially nm23-H1, is activated, accompanied by c-erbB-2 and c-erbB-3 overexpressions, in early stages of the carcinogenic process of ovarian carcinoma and reduction of nm23-H1 expression occurs in association with lymph nodal and/or distant metastasis.

MeSH Terms
Adenocarcinoma/genetics,metabolism,pathology Base Sequence DNA Primers ErbB Receptors/biosynthesis,genetics Female Gene Expression Humans Immunohistochemistry Molecular Sequence Data Monomeric GTP-Binding Proteins NM23 Nucleoside Diphosphate Kinases Neoplasm Metastasis Neoplasm Staging Nucleoside-Diphosphate Kinase/biosynthesis,genetics Oligonucleotide Probes Ovarian Neoplasms/genetics,metabolism,pathology Ovary/metabolism Polymerase Chain Reaction Proto-Oncogene Proteins/biosynthesis,genetics Proto-Oncogenes RNA, Messenger/biosynthesis,metabolism Receptor, ErbB-2 Receptor, ErbB-3 Receptors, Estrogen/analysis,biosynthesis Receptors, Progesterone/analysis,biosynthesis Transcription Factors/biosynthesis,genetics
Chemicals
DNA Primers NM23 Nucleoside Diphosphate Kinases Oligonucleotide Probes Proto-Oncogene Proteins RNA, Messenger Receptors, Estrogen Receptors, Progesterone Transcription Factors ErbB Receptors Receptor, ErbB-2 Receptor, ErbB-3 NME1 protein, human Nucleoside-Diphosphate Kinase Monomeric GTP-Binding Proteins
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Mandai M
Department of Pathology, Faculty of Medicine, Kyoto University, Japan.
Konishi I
Koshiyama M
Mori T
Arao S
Tashiro H
Okamura H
Nomura H
Hiai H
Fukumoto M
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1994-04-01
Pages
1825-30
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
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