Downregulation of PD-L1 via FKBP5 by celecoxib augments antitumor effects of PD-1 blockade in a malignant glioma model

• Material Type: 博士論文
• ISSN: 2632-2498
• Title: Downregulation of PD-L1 via FKBP5 by celecoxib augments antitumor effects of PD-1 blockade in a malignant glioma model
• Volume: 2 1
• Author/Editor: Yamaguchi, Izumi; Nakajima, Kohei; Shono, Kenji; Mizobuchi, Yoshifumi; Fujihara, Toshitaka; Shikata, Eiji; Yamaguchi, Tadashi; Kitazato, Keiko; Sampetrean, Oltea; Saya, Hideyuki; Takagi, Yasushi
• Author Heading: Yamaguchi, Izumi; Nakajima, Kohei; Shono, Kenji; Mizobuchi, Yoshifumi; Fujihara, Toshitaka; Shikata, Eiji; Yamaguchi, Tadashi; Kitazato, Keiko; Sampetrean, Oltea; Saya, Hideyuki; Takagi, Yasushi
• Publication, Distribution, etc.: Oxford University Press|the Society for Neuro-Oncology|the European Association of Neuro-Oncology
• Publication Date: 2019-12-26
• Publication Date (W3CDTF): 2019-12-26
• Alternative Title: セレコキシブによるFKBP5を介したPD-L1の発現低下は, 悪性神経膠腫モデルにおける抗PD-1抗体医薬による抗腫瘍効果を増強する; FKBP5 regulation on anti-PD-1 therapy
• Periodical title: Neuro-Oncology Advances
• Degree grantor/type: 徳島大学
• Date Granted: 2020-03-23
• Date Granted (W3CDTF): 2020-03-23
• Dissertation Number: 甲第3370号
• Degree Type: 博士（医学）
• Conferring No. (Dissertation): 甲第3370号
• Text Language Code: eng
• Subject Heading: glioblastoma; PD-1; PD-L1; FKBP5; celecoxib
• Target Audience: 一般
• Note (General): Background. Antitumor therapies targeting programmed cell death-1 (PD-1) or its ligand-1 (PD-L1) are used in various cancers. However, in glioblastoma (GBM), the expression of PD-L1 varies between patients, and the relationship between this variation and the efficacy of anti-PD-1 antibody therapy remains unclear. High expression levels of PD-L1 affect the proliferation and invasiveness of GBM cells. As COX-2 modulates PD-L1 expression in cancer cells, we tested the hypothesis that the COX-2 inhibitor celecoxib potentiates anti-PD-1 antibody treatment via the downregulation of PD-L1.Methods. Six-week-old male C57BL/6 mice injected with murine glioma stem cells (GSCs) were randomly divided into four groups treated with vehicle, celecoxib, anti-PD-1 antibody, or celecoxib plus anti-PD-1 antibody and the antitumor effects of these treatments were assessed. To verify the mechanisms underlying these effects, murine GSCs and human GBM cells were studied in vitro.Results. Compared with that with each single treatment, the combination of celecoxib and anti-PD-1 antibody treatment significantly decreased tumor volume and prolonged survival. The high expression of PD-L1 was decreased by celecoxib in the glioma model injected with murine GSCs, cultured murine GSCs, and cultured human GBM cells. This reduction was associated with post-transcriptional regulation of the co-chaperone FK506-binding protein 5 (FKBP5).Conclusions. Combination therapy with anti-PD-1 antibody plus celecoxib might be a promising therapeutic strategy to target PD-L1 in glioblastoma. The downregulation of highly-expressed PD-L1 via FKBP5, induced by celecoxib, could play a role in its antitumor effects.
• DOI: info:doi/10.1093/noajnl/vdz058; https://doi.org/info:doi/10.1093/noajnl/vdz058
• Persistent ID (NDL): info:ndljp/pid/11498502; https://dl.ndl.go.jp/pid/11498502
• Collection: 障害者向け資料
• Collection (Materials For Handicapped People:1): テキストデータ
• Collection (particular): 国立国会図書館デジタルコレクション > デジタル化資料 > 博士論文; https://dl.ndl.go.jp/collections/A00014
• Acquisition Basis: 博士論文（自動収集）
• Date Accepted (W3CDTF): 2020-06-07T00:39:19+09:00
• Format (IMT): application/pdf
• Access Restrictions: 国立国会図書館内限定公開
• Service for the Digitized Contents Transmission Service: 図書館・個人送信対象外
• Availability of remote photoduplication service: 可
• Periodical Title (URI): http://repo.lib.tokushima-u.ac.jp/114665
• Data Provider (Database): 国立国会図書館 : 国立国会図書館デジタルコレクション; https://dl.ndl.go.jp