Pathology, Pathogenesis and Therapy of Growth Hormone (GH)-producing Pituitary Adenomas: Technical Advances in Histochemistry and Their Contribution

被引:12
|
作者
Osamura, Robert Y. [1 ]
Egashira, Noboru [1 ]
Kajiya, Hanako [1 ]
Takei, Mao [1 ,2 ]
Tobita, Maya [1 ,3 ]
Miyakoshi, Takashi [1 ]
Inomoto, Chie [1 ]
Takekoshi, Susumu [1 ]
Teramoto, Akira [2 ]
机构
[1] Tokai Univ, Sch Med, Dept Pathol, Isehara, Kanagawa 2591193, Japan
[2] Nippon Med Sch, Dept Neurosurg, Bunkyo Ku, Tokyo 1138603, Japan
[3] Jikei Univ, Sch Med, Div Endocrinol Diabet & Metab, Minato Ku, Tokyo 1058461, Japan
关键词
pituitary adenoma; transcription factor; cell lineage; functional differentiation; pituitary hormones; TRANSGENIC MICE; MESSENGER-RNA; CELL-LINE; EXPRESSION; GENE; TRANSCRIPTION; TUMOR; PIT-1; GH; DIFFERENTIATION;
D O I
10.1267/ahc.09004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Growth hormone (GH)-producing adenomas (GHomas) are one of the most frequently-occurring pituitary adenomas. Differentiation of hormone-producing cells in the pituitary gland is regulated by transcription factors and co-factors. The transcription factors include Pit-1, Prop-1, NeuroD1, Tpit, GATA-2, SF-1. Aberrant expression of transcription factors such as Pit-1 results in translineage expression of GH in adrenocorticotropic hormone-producing adenomas (ACTHomas). This situation has been substantiated by GFP-Pit-1 transfection expression in the AtT20 cell line. Experimentally, GHomas have been induced in GH-releasing hormone (GHRH) or Prop-1 transgenic animals. Immunohistochemical detection of somatostatin receptor (SSTR2a) has recently emphasized their role in the response of GHomas to somatostatin analogue therapy. In this review, the advances in technology and their contribution to cell biology and medical practice are discussed.
引用
收藏
页码:95 / 104
页数:10
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