| Project/Area Number |
10671328
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Cerebral neurosurgery
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| Research Institution | Nippon Medical School |
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Principal Investigator |
SANNO Naoko Nippon Medical School, Departoment of Neurosurgery, Assistant Professor, 医学部, 講師 (90297862)
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| Co-Investigator(Kenkyū-buntansha) |
KOMATSUBARA Kiyoteru Nippon Medical School, Departoment of Neurosurgery, Fellow, 医学部, 助手 (10318496)
TAHARA Shigeyuki Nippon Medical School, Departoment of Neurosurgery, Fellow, 医学部, 助手 (80277540)
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| Project Period (FY) |
1998 – 1999
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| Project Status |
Completed (Fiscal Year 1999)
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| Budget Amount *help |
¥2,700,000 (Direct Cost: ¥2,700,000)
Fiscal Year 1999: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 1998: ¥2,000,000 (Direct Cost: ¥2,000,000)
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| Keywords | nuclear receptor / transcription / Pituitary / receptor / transcription factor / mRNA / polymerase chain reaction / mRNA / 核内レセプター / 下垂体 / 下垂体腺腫 / 転写因子 / レチノイド / 遺伝子 / PCR |
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| Research Abstract |
The production of hormounes in the anterio pituitary gland is under the control of several factors. Our previous studies on human pituitary adenomas disclosed the possiblity of pituitary specific transcriptional factor, Pit-1 participation in the hunctional differentiation of the tumor cells. Nuclear receptors such as estrogen receptor (ER), retinoic acid receptor, retinoid X receptor (RXR) have been known to have important roles as transcriptional factors in synergy with specific transcription factors. We investigated the expression those nuclear receptors in human pituitaries and human pituitary adenomas to clarify the roles on functional differentiation of pituitary cells. Using various techniques including immunohistochemistry, western blotting, in situ hybridization, reverse transcription polymerase chain reaction (RT-PCR) and in situ RT-PCR, it has been suggested that Pit-1 may have a role in the functional differentiation of GH, PRL and TSH cells. It has been suggested that ER functions synergistically in PRL secreting adenomas. The expression of RXRg isoform was identified in GH and TSH cells and the contribution on multihormonality of GH, and TSH secreting adenomas was suggested. Furthermore, we have investigated the expression of hypothalamic hormones, hypothalamic hormone receptors and some recently recognized transcription factors. Possible synergistic with those factors remain to be elucidated.
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