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Expression of nm 23‐Hl and nm 23‐H2 Proteins in Prostate Carcinoma
Author(s) -
Konishi Noboru,
Nakaoka Shingo,
Tsuzuki Toshihide,
Matsumoto Kyoichi,
Kitahori Yoshiteru,
Hiasa Yoshio,
Urano Takeshi,
Shiku Hiroshi
Publication year - 1993
Publication title -
japanese journal of cancer research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.035
H-Index - 141
eISSN - 1349-7006
pISSN - 0910-5050
DOI - 10.1111/j.1349-7006.1993.tb02800.x
Subject(s) - immunostaining , prostate , pathology , carcinoma , immunohistochemistry , hyperplasia , staining , cancer research , medicine , cancer
The nm 23 gene products/nucleoside diphosphate (NDP) kinase expression in prostate carcinomas and benign hyperplasias was evaluated immunohistochemically. Monoclonal antibodies against nm 23‐H1 and nm 23‐H2 proteins were prepared using the corresponding proteins fused with glutathione S‐transferase as immunogens. Of the 80 cases of nonmetastatic prostate carcinoma examined, 74% (59/80) and 60% (48/80) were immunoreactive for nm 23‐H1 or nm 23‐H2 protein, respectively. Negative staining for nm 23‐H1 occurred in 83% of metastatic lesions, while 34% were negative for nm 23‐H2. All primary tumors corresponding to the metastases examined showed positive immunostaining for nm 23‐H1, indicating an inverse relationship between expression of this protein and metastatic status. nm 23‐H2 protein was detected in 83% of primary tumors and its expression appeared to he significantly correlated to the degree of histological differentiation. In contrast, all cases of benign prostatic hyperplasia showed elevated levels of both nm 23‐H1 and nm 23‐H2 expression. These data suggest that the nm 23/NDP kinase may play a role in suppressing the expression of malignant potential in prostate carcinomas.

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