Volume 46, Issue 2 pp. 202-208

Overexpression of Ets-1 proto-oncogene in latent and clinical prostatic carcinomas

G Alipov

G Alipov

Tissue and Histopathology Section, Division of Scientific Data Registry

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T Nakayama

T Nakayama

Department of Molecular Pathology, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki

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M Ito

M Ito

Department of Pathology, National Nagasaki Medical Center, Omura

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K Kawai

K Kawai

Department of Pathology, Nagasaki Municipal Hospital, Nagasaki,

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S Naito

S Naito

Department of Pathology, Ureshino National Hospital, Saga, Japan

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M Nakashima

M Nakashima

Tissue and Histopathology Section, Division of Scientific Data Registry

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D Niino

D Niino

Department of Molecular Pathology, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki

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I Sekine

I Sekine

Tissue and Histopathology Section, Division of Scientific Data Registry

Department of Molecular Pathology, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki

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First published: 05 February 2005
Citations: 47
Toshiyuki Nakayama MD, PhD, Department of Molecular Pathology, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan. e-mail: [email protected]

Abstract

Aims : The high incidence of clinically diagnosed prostatic cancer is exceeded by the frequency of tumours detected at autopsy. The Ets-1 proto-oncogene is expressed by a variety of malignant and normal tissues. Therefore, in this study, expression of Ets-1 protein was investigated in ‘latent’ prostatic cancer detected at autopsy, compared with benign prostatic hyperplasia, normal prostatic tissues and clinical prostatic cancer.

Methods and results : Using immunohistochemistry, we analysed Ets-1 expression in 95 prostatic specimens including 19 cases of latent prostatic carcinoma (LPC) and 55 cases of clinical prostatic carcinoma (CPC), 11 cases of benign prostatic hyperplasia (BPH) and 10 cases of normal prostate (NP). Differences in the incidence of LPC and CPC suggest different courses for the biological progression of prostatic cancer. There was a significant difference in the degree of Ets-1 expression in CPC and LPC (P < 0.05). Ets-1 was not expressed in BPH and NP, but in malignant cases (57 of 74; 77.0%) commonly demonstrated immunoreactivity in the tumour cells. In our study the expression of Ets-1 between benign and malignant, and well, moderately and poorly differentiated adenocarcinomas of prostatic cancer showed significant differences. The presence of Ets-1 mRNA was confirmed by in-situ hybridization in human prostatic tissues.

Conclusion : Our results suggest that Ets-1 might play an important role in carcinogenesis and/or the progression of human prostatic carcinomas.

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