| Project/Area Number |
18K06995
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Review Section |
Basic Section 49020:Human pathology-related
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| Research Institution | Tohoku Medical and Pharmaceutical University |
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Principal Investigator |
Hata Shuko 東北医科薬科大学, 医学部, 助教 (90466532)
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| Co-Investigator(Kenkyū-buntansha) |
中村 保宏 東北医科薬科大学, 医学部, 教授 (80396499)
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| Project Period (FY) |
2018-04-01 – 2023-03-31
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| Project Status |
Completed (Fiscal Year 2022)
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| Budget Amount *help |
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2020: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2019: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2018: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
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| Keywords | 前立腺癌 / GR / SGK1 / NDRG1 / primary tumor (pT) stage / PER1 / GRβ / グルココルチコイド受容体 / デキサメタゾン / ステロイドホルモン |
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| Outline of Final Research Achievements |
Glucocorticoid receptor (GR) has been implicated in prostate carcinoma growth and progression. The association between the status of GR, GRβ, SGK1, and NDRG1 immunoreactivity and clinicopathological variables was analyzed in patients with prostate carcinoma to explore their clinical significance. In prostate carcinoma cases, the relative abundance of GR and NDRG1 immunoreactivity was inversely and significantly associated with the primary tumor stage (pT), while GR immunoreactivity was inversely and significantly associated with the Ki67 score. The relative expression status of NDRG1 was significantly associated with that of GR. However, no significant correlation was observed between any of the clinicopathological parameters and GRβ and SGK1 expression. Our findings indicate that GR and NDRG1 expression status is correlated with clinicopathological features in patients with prostate cancer.
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| Academic Significance and Societal Importance of the Research Achievements |
GRは癌の増殖や進展に関与している可能性が示唆されているが、臓器によって影響が異なる報告がなされており、前立腺癌においても十分に解明されていない。本研究では、GRとその関連因子の発現状況を検討した。GRおよびNDRG1は癌の初期に高発現し、癌抑制に働いており、発現が低下すると癌の進展が抑制されなくなることが示唆された。これらの発現状況を検討することで前立腺癌患者の予後予測に寄与する可能性を示した。
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