Updated on 2025/04/04

写真a

 
Miura Noriyoshi
 
Organization
University Hospital Associate Professor
Title
Associate Professor
Contact information
メールアドレス
External link

Degree

  • 博士 ( 愛媛大学 )

Research Areas

  • Life Science / Urology

Papers

  • The Prognostic Impact of Intraductal Carcinoma of the Prostate: A Systematic Review and Meta-Analysis Reviewed International journal

    Miura N, Mori K, Mostafaei H, Quhal F, Motlagh RS, Pradere B, Laukhtina E, D'Andrea D, Saika T, Shariat SF

    Journal of Urology   204 ( 5 )   909 - 917   2020.11

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    PURPOSE: This systematic review and meta-analysis aimed to assess the prognostic impact of intraductal carcinoma of the prostate in patients with prostate cancer. MATERIALS AND METHODS: A systematic search was performed according to the Preferred Reporting Items for Systematic Review and Meta-Analysis statement. We searched PubMed®, Web of Science™, the Cochrane Library and Scopus® up to October 2019. The end points were biochemical recurrence-free, cancer specific and overall survival. RESULTS: We identified 32 studies with 179,766 patients. A total of 31 studies containing 179,721 patients with localized and advanced prostate cancer were eligible for meta-analysis. In localized prostate cancer intraductal disease was associated with adverse outcomes including lower biochemical recurrence-free survival (pooled HR 2.09, 95% CI 1.75-2.50) and cancer specific survival (pooled HR 2.93, 95% CI 2.25-3.81). In advanced prostate cancer overall survival was lower in patients with vs without intraductal disease (pooled HR 1.75, 95% CI 1.43-2.14). Subgroup analysis by specimen type revealed that intraductal carcinoma of the prostate is a significant negative prognostic factor in both biopsies and prostatectomy specimens. Moreover, subgroup analyses based on the histopathological definitions of intraductal carcinoma of the prostate indicated that intraductal disease was significantly associated with lower biochemical recurrence-free, cancer specific and overall survival for almost all definitions. CONCLUSIONS: Intraductal disease is a histopathological feature of biologically and clinically aggressive prostate cancer. It confers worse oncologic outcomes in both localized and advanced prostate cancer, whether assessed in biopsy or prostatectomy specimen. The pathologist should assess for and report on the presence of intraductal disease in all prostate specimens. The urologist and radiation oncologist should consider this adverse feature in their clinical decision making.

    File: J Urol 2020 IDC-P.pdf

    DOI: 10.1097/JU.0000000000001290

    PubMed

    researchmap

  • Prognostic value of testosterone for the castration-resistant prostate cancer patients: a systematic review and meta-analysis. Reviewed

    Miura N, Mori K, Mostafaei H, Quhal F, Sari Motlagh R, Abufaraj M, Pradere B, Aydh A, Laukhtina E, D'Andrea D, Saika T, Shariat SF

    Int J Clin Oncol   25 ( 11 )   1881 - 1891   2020.11

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    INTRODUCTION: This systematic review and meta-analysis aimed to assess the prognostic value of testosterone in patients with castration-resistant prostate cancer (CRPC). MATERIALS AND METHODS: PubMed, Web of Science, and Scopus databases were systematically searched until December 2019, according to the Preferred Reporting Items for Systemic Review and Meta-analysis statement. The endpoints were progression-free survival (PFS) and overall survival (OS). RESULTS: We identified 11 articles with 4206 patients for systematic review and nine articles with 4136 patients for meta-analysis. Higher testosterone levels were significantly associated with better OS (pooled HR 0.74, 95% CI 0.58-0.95) and better PFS (pooled HR 0.51, 95% CI 0.30-0.87). Subgroup analyses based on the treatment type revealed that higher testosterone levels were significantly associated with better OS in CRPC patients treated with androgen receptor-targeted agents (ARTAs) (pooled HR 0.64, 95% CI 0.55-0.75), but not in those treated with chemotherapy (pooled HR 0.78, 95% CI 0.53-1.14). CONCLUSION: This meta-analysis demonstrated that the PFS and OS were significantly greater in patients with CRPC in those with higher testosterone levels than that of those with lower testosterone levels. In the subgroup analyses, lower testosterone levels were a consistently poor prognostic factor for OS in patients treated with ARTAs, but not in those treated with chemotherapy. Therefore, higher testosterone levels could be a useful biomarker to identify patient subgroups in which ARTAs should be preferentially recommended in the CRPC setting.

    File: Miura2020_Article_PrognosticValueOfTestosteroneF.pdf

    DOI: 10.1007/s10147-020-01747-1

    PubMed

    researchmap

  • Vesicles Secreted by Renal Cell Carcinoma Cells Cause Vascular Endothelial Cells to Express PSMA and Drive Tumor Progression. International journal

    Ryuta Watanabe, Keito Kagimoto, Mami Chosei, Tomohisa Sakaue, Mie Kurata, Noriyoshi Miura, Riko Kitazawa, Tadahiko Kikugawa, Shigeki Higashiyama, Takashi Saika

    Cells   14 ( 3 )   2025.1

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    Prostate-specific membrane antigen (PSMA) protein expression is induced during prostate cancer progression and metastasis. Recently, we reported that PSMA-positive vesicles released by prostate cancer cell lines enhanced vascular endothelial cell angiogenesis and that PSMA may be involved in tumor angiogenesis. Similarly, it is known that PSMA is upregulated in peritumoral vessels in renal cell carcinoma (RCC). In this study, we investigated the significance and molecular function of PSMA in RCC. PSMA immunohistochemical staining confirmed PSMA presence only in perinephric tumor vessels, and PSMA intensity was strongly correlated with recurrence rate and venous invasion. Spatial gene expression analysis revealed that FOLH1 expression, which codes PSMA, was upregulated in tumor blood vessels around renal cancer, and that angiogenesis-related pathways were enhanced. The 10,000 g pellet fraction of the renal cancer cell lines Caki1- and ACHN-conditioned medium (CM) induced PSMA positivity in human umbilical vein endothelial cells (HUVECs) and enhanced tube formation. Mass spectrometry indicated that the 10,000 g pellet fraction contained various kinds of growth factors, like GDF15 and MYDGF. RNA sequencing showed that supplementing HUVECs with RCC cell CM-enhanced angiogenesis-related signaling pathways. Conclusively, microvesicle components secreted by RCC cells transform vascular endothelial cells into PSMA-positive cells, enhancing angiogenesis.

    DOI: 10.3390/cells14030165

    PubMed

    researchmap

  • Genetic Analysis of Intraductal Carcinoma of the Prostate Detected in High-Grade Prostatic Intraepithelial Neoplasia Cases. International journal

    Ryuta Watanabe, Noriyoshi Miura, Mie Kurata, Riko Kitazawa, Tadahiko Kikugawa, Takashi Saika

    Cureus   16 ( 12 )   e76165   2024.12

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    Background The accurate diagnosis of intraductal carcinoma of the prostate (IDC-P) is occasionally challenging due to the similarity in pathological morphology between IDC-P and high-grade prostatic intraepithelial neoplasia (HGPIN). In this report, we reviewed the pathology of cases previously diagnosed as HGPIN to search for IDC-P cases effectively. In addition, we examined whether those cases had genetic abnormalities. Methods We reviewed 98 patients with HGPIN who underwent prostatectomy at our hospital between 2011 and 2021. They were reviewed by three pathologists to search for IDC-P findings by adding immunostaining for basement membrane markers. Genetic testing of prostatectomy specimens was performed to identify the presence of gene mutations. Results The typical IDC-P was diagnosed in two of the 98 patients. The Gleason score of background prostate cancer (PCa) was 4+5 and 4+4. Genetic testing revealed several mutations in DNA repair-related genes, such as CHEK2, FANCC, TOE1, RECQL, USG2A, and PRPF31. The pathological significance of these mutations has conflicting interpretations, as referenced in the ClinVar. Conclusions IDC-P cases can be identified from past HGPIN cases, and cases with genetic abnormalities of conflicting pathological significance can be efficiently detected. Accurate diagnosis of IDC-P enables early intervention with precision medicine for PCa. It is useful to pay attention to HGPIN cases to avoid missing true IDC-P.

    DOI: 10.7759/cureus.76165

    PubMed

    researchmap

  • 高齢前立腺癌患者におけるダロルタミドの使用経験

    大西 智也, 大川 大, 坂本 みき, 澤田 貴虎, 西田 敬悟, 渡辺 隆太, 西村 謙一, 福本 哲也, 三浦 徳宣, 宮内 勇貴, 菊川 忠彦, 雑賀 隆史

    西日本泌尿器科学会総会抄録集   76回   264 - 264   2024.10

     More details

    Language:Japanese   Publisher:(一社)西日本泌尿器科学会  

    researchmap

▼display all

MISC

  • イピリムマブ・ニボルマブ併用療法においてCD21<sup>lo</sup>B細胞は免疫学的有害事象の予測因子になりうる

    西村謙一, 小西達也, 越智俊元, 渡辺隆太, 野田輝乙, 福本哲也, 三浦徳宣, 宮内勇貴, 菊川忠彦, 雑賀隆史

    泌尿器科分子・細胞研究会プログラム・抄録集   32nd   2023

  • 進行胃癌に対するニボルマブ投与中に生じた難治性頻尿の1例

    杉原直哉, 塩出涼, 鈴木大一郎, 信森祥太, 佐伯佳央里, 山川真季, 河野玲奈, 渡辺隆太, 野田輝乙, 西村謙一, 福本哲也, 三浦徳宣, 宮内勇貴, 菊川忠彦, 雑賀隆史

    日本排尿機能学会誌(Web)   33 ( 1 )   2022

  • 広汎子宮全摘除術後に自己導尿を要した患者の検討

    西村謙一, 塩出涼, 鈴木大一郎, 信森祥太, 杉原直哉, 山川真季, 佐伯佳央里, 河野玲奈, 渡辺隆太, 野田輝乙, 福本哲也, 三浦徳宣, 宮内勇貴, 菊川忠彦, 雑賀隆史, 宇佐美知香

    日本排尿機能学会誌(Web)   33 ( 1 )   2022

  • ロボット支援仙骨膣固定術の下部尿路障害に対する治療成績

    福本哲也, 信森祥太, 鈴木大一郎, 塩出涼, 杉原直哉, 山川真季, 佐伯佳央里, 河野玲奈, 渡辺隆太, 野田輝乙, 西村謙一, 三浦徳宣, 宮内勇貴, 菊川忠彦, 雑賀隆史

    日本排尿機能学会誌(Web)   33 ( 1 )   2022

  • エベロリムス周術期add-onプロトコルの検討

    宮内勇貴, 杉原直哉, 佐伯佳央里, 山川真季, 河野玲奈, 渡辺隆太, 野田輝乙, 西村謙一, 福本哲也, 三浦徳宣, 菊川忠彦, 雑賀隆史, 莖田昌敬

    日本移植学会総会プログラム抄録集   58th (Web)   2022

▼display all

Research Projects

  • 前立腺癌骨転移の分子メカニズム解明と革新的治療法開発への基盤的研究

    2024.4 - 2027.3

    日本学術振興会  科学研究費助成事業  基盤研究(C)

    雑賀 隆史, 新井 欧介, 今井 祐記, 柳原 裕太, 菊川 忠彦, 三浦 徳宣

      More details

    Grant amount:\4680000 ( Direct Cost: \3600000 、 Indirect Cost:\1080000 )

    researchmap

  • 前立腺癌スフェロイドのシングルセル解析による導管内浸潤前立腺癌の病態解明

    2024.4 - 2027.3

    日本学術振興会  科学研究費助成事業  基盤研究(C)

    三浦 徳宣, 渡辺 隆太, 雑賀 隆史, 菊川 忠彦

      More details

    Grant amount:\4680000 ( Direct Cost: \3600000 、 Indirect Cost:\1080000 )

    researchmap

  • 数値流体計算を用いた腎盂内圧力変化の解析と腎盂内圧が腎機能へ与える影響

    2024.4 - 2027.3

    日本学術振興会  科学研究費助成事業  基盤研究(C)

    西村 謙一, 雑賀 隆史, 中村 匡徳, 菊川 忠彦, 三浦 徳宣

      More details

    Grant amount:\3900000 ( Direct Cost: \3000000 、 Indirect Cost:\900000 )

    researchmap

  • International collaboration research on the identification of novel driver genes for prostate cancer by single cell analysis.

    2022.10 - 2026.3

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Fund for the Promotion of Joint International Research (Fostering Joint International Research (B))

      More details

    Grant amount:\20150000 ( Direct Cost: \15500000 、 Indirect Cost:\4650000 )

    researchmap

  • シングルセル解析による腫瘍微小環境を介した前立腺神経内分泌腫瘍発生機序の解明

    2022.4 - 2025.3

    日本学術振興会  科学研究費助成事業  基盤研究(C)

    渡辺 隆太, 雑賀 隆史, 東山 繁樹, 菊川 忠彦, 三浦 徳宣, 沢田 雄一郎

      More details

    Grant amount:\4160000 ( Direct Cost: \3200000 、 Indirect Cost:\960000 )

    researchmap

▼display all