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Pit‐1 gene expression in human pituitary adenomas using the reverse transcription polymerase chain reaction method

 

作者: Shozo Yamada,   Michie Takahashi,   Masayuki Hara,   Atsuhiko Hattori,   Toshiaki Sano,   Yasunori Ozawa,   Yoshimasa Shishiba,   Kazuaki Hirata,   Masaaki Usui,  

 

期刊: Clinical Endocrinology  (WILEY Available online 1996)
卷期: Volume 45, issue 3  

页码: 263-272

 

ISSN:0300-0664

 

年代: 1996

 

DOI:10.1046/j.1365-2265.1996.00812.x

 

出版商: Blackwell Science Ltd

 

数据来源: WILEY

 

摘要:

OBJECTIVE Previous studies of Pit‐1 expression in human pituitary tumours have produced conflicting results. We have studied expression of Pit‐1 mRNA in human pituitary adenomas, as well as in normal human and rat pituitaries, and results were compared with clinical, histological, and immunohistochemical features. In addition, expression of GH, PRL, and TSH‐β mRNA was also studied and compared with Pit‐1 gene expression.MATERIAL AND METHODS The adenomas consisted of 13 GH cell adenomas, 7 PRL cell adenomas, 3 TSH cell adenomas, 4 ACTH cell adenomas, and 10 clinically non‐functioning adenomas. Expression of the Pit‐1, its isoforms, and each hormone, was studied using the reverse transcription polymerase chain reaction.RESULTS Pit‐1 mRNA was expressed not only in normal human and rat pituitaries, but also in all GH, PRL and TSH cell adenomas. There was no correlation between Pit‐1 transcripts and biological behaviour or histological findings in these three types of adenoma, suggesting that Pit‐1 is generally required for the determination of cell phenotype but is insufficient for the regulation of hormonal activity and tumour growth in these pituitary adenomas. In addition, Pit‐1 was also expressed in some ACTH cell (2/4) and non‐functioning adenomas (7/10). Although there were no GH, PRL or TSH‐β transcripts in Pit‐1 mRNA‐negative ACTH cell and non‐functioning adenomas, PRL mRNA was detected in all Pit‐1 mRNA‐positive ACTH cell adenomas and GH, PRL and/or TSH‐β mRNA were found in four of seven Pit‐1 mRNA‐positive non‐functioning adenomas. In contrast, Pit‐1 mRNA was expressed without any GH, PRL, or TSH‐β transcripts in only three non‐functioning adenomas. These data suggest that expression of Pit‐1 mRNA in these two types of adenomas can be mainly attributed to the presence of GH, PRL and/or TSH‐β mRNA expressing cells and that true Pit‐1 transcripts found in non‐functioning adenomas may be a rare event. Moreover, there were two cases which expressed Pit‐1α mRNA, but failed to show other Pit‐1 isoform mRNA. There were, however, no clinical or histological differences between these two adenomas showing only Pit‐1α mRNA and the others expressing both Pit‐1α mRNA and other Pit‐1 isoform mRNA.CONCLUSIONS Pit‐1 mRNA was expressed not only in GH, PRL and TSH cell adenomas but also in other types of adenoma. However, it is suggested that expression of Pit‐1 mRNA in most ACTH cell and non‐functioning adenomas can be attributed to GH, PRL and/or TSH‐β mRNA expressing cells. Further studies are necessary to elucidate the role of Pit‐1 tr

 

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