2020 Fiscal Year Final Research Report
Are bioactive substances produced in the anterior pituitary gland involved in the formation of prolactin-producing tumors?
Project/Area Number |
17K08517
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
General anatomy (including histology/embryology)
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Research Institution | Kanagawa University (2020) Jichi Medical University (2017-2019) |
Principal Investigator |
Fujiwara Ken 神奈川大学, 理学部, 准教授 (00382945)
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Co-Investigator(Kenkyū-buntansha) |
屋代 隆 自治医科大学, 医学部, 教授 (80119859)
東 森生 自治医科大学, 医学部, 講師 (90709643)
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Project Period (FY) |
2017-04-01 – 2021-03-31
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Keywords | 下垂体前葉 / 腫瘍 / 細胞間相互作用 / 局所環境 / 細胞増殖因子 / 幹細胞 / 分化 |
Outline of Final Research Achievements |
Pituitary tumors cause serious endocrine disease, but the mechanism of tumorigenesis remains unclear in many cases. Therefore, in this study, we used estrogen-induced prolactin-producing tumor model rats, then examined whether bioactive substances (cytokines, growth factors, etc.) produced in the anterior pituitary gland are involved in tumorigenesis. As a result, we found several bioactive substances and their receptors that increase during the formation of prolactin-producing tumors. It is suggested that these molecules are involved in the formation of prolactin-producing tumors, and the results of this study will contribute to the elucidation of new mechanisms of pituitary tumorigenesis.
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Free Research Field |
内分泌学、組織学
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Academic Significance and Societal Importance of the Research Achievements |
本研究の成果は、プロラクチン産生腫瘍の新たな要因としての治療介入のポイントを与えることにつながると考える。特に、本研究で焦点としている生理活性物質が、Gタンパク質結合型受容体もしくは酵素連結型受容体のリガンドであり、今後の創薬のターゲットとなることが予想される。また、下垂体前葉の腫瘍形成のメカニズムの解明に大きく貢献することが期待される。
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