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20 March 1997, Volume 14, Number 11, Pages 1377-1382
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Short report
Cloning of human bone morphogenetic protein type IB receptor (BMPR-IB) and its expression in prostate cancer in comparison with other BMPRs
Hisamitsu Ide1,2,3, Masaru Katoh1, Hiroki Sasaki1, Teruhiko Yoshida1, Kazunori Aoki1, Yukifumi Nawa2, Yukio Osada3, Takashi Sugimura1 and Masaaki Terada1,a

1Genetics Division, National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104, Japan

2Department of Parasitology, Miyazaki Medical College, 5200 Kiyotake, Miyazaki 889 - 16, Japan

3Department of Urology, Miyazaki Medical College, 5200 Kiyotake, Miyazaki 889 - 16, Japan

aAuthor for correspondence

Abstract

Bone metastasis is a common event in prostate cancer, and it is known that some of the bone morphogenetic proteins (BMPs) are expressed in prostate cancer cells, while no study on the expression of their receptors, BMPRs, has been reported. Here we report cloning and sequence analysis of the human BMPR-IB cDNA. We also analysed the expression of transcripts of three types of the BMPR genes in human tissues and prostate cancer cell lines. The BMPR-IB mRNA was present in various organs, but the highest level was found in the prostate. Moreover, the amount of BMPR-IB mRNA was significantly low in prostate cancer tissues after androgen withdrawal and was also low in prostate cancer cell lines. RT - PCR analysis showed that the BMPR-IB message was upregulated by androgen stimulation in the LNCaP cell line which expresses the androgen receptor. By contrast, the mRNA levels of BMPR-IA and BMPR-II were not significantly different among non-cancerous and cancerous prostate tissues. It was also suggested that human BMPR-IA and BMPR-IB might have different biological functions in the prostate, although their sequences were 85.3% identical in the serine-threonine kinase domain.

Keywords

bone morphogenetic protein receptor; prostate cancer; human BMPR-IB

Received 29 August 1999; revised 14 November 1999; accepted 15 November 1999
20 March 1997, Volume 14, Number 11, Pages 1377-1382
Table of contents    Previous  Abstract  Next   Article  PDF
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