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博士論文

GSK-3β mediates the effects of HNF-1β overexpression in ovarian clear cell carcinoma. 20 5

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GSK-3β mediates the effects of HNF-1β overexpression in ovarian clear cell carcinoma. 5

Persistent ID (NDL)
info:ndljp/pid/12070977
Material type
博士論文
Author
Kawahara, Naokiほか
Publisher
Spandidos
Date granted
2021-03-15
Material Format
Digital
Capacity, size, etc.
-
Degree grantor and degree
奈良県立医科大学,博士(医学)
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type:ThesisDeubiquitinase USP28 is a target gene of the transcription factor HNF1 homeobox β (HNF-1β), which promotes the survival of ovarian clear ce...

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Digital

Material Type
博士論文
Volume
20 5
Author/Editor
Kawahara, Naoki
Mizutani, Ayano
Matsubara, Sho
Takeda, Yoshinori
Kobayashi, Hiroshi
Publication, Distribution, etc.
Publication Date
2020-11
20 5
Publication Date (W3CDTF)
2020-11
Alternative Title
HNF-1β過剰発現を呈する卵巣明細胞癌においてGSK-3βは新たなシグナル伝達経路を介在する
Periodical title
Experimental and therapeutic medicine
Pages
Article No.122-
ISSN (Periodical Title)
17920981
Degree Grantor
奈良県立医科大学
Date Granted
2021-03-15
Date Granted (W3CDTF)
2021-03-15
Dissertation Number
甲第785号
Degree Type
博士(医学)
Conferring No. (Dissertation)
甲第785号
Text Language Code
eng
Target Audience
一般
Note (General)
type:Thesis
Deubiquitinase USP28 is a target gene of the transcription factor HNF1 homeobox β (HNF-1β), which promotes the survival of ovarian clear cell carcinoma (OCCC) cell lines. However, the pharmacological inhibition of HNF-1β can cause several adverse effects as it is abundantly expressed in numerous organ systems, including the kidney, liver, pancreas and digestive tract. Therefore, small interfering RNA (siRNA) screening was performed in the current study to identify other potential downstream targets of the HNF-1β-mediated pathway. The results revealed that glycogen synthase kinase-3β (GSK-3β) may be a potential downstream target affecting cell viability. To further clarify the effects of GSK-3β, two human OCCC cell lines, TOV-21G (HNF-1β overexpressing line) and ES2 (HNF-1β negative) were transfected with siRNA targeting GSK-3β or control vectors. Loss-of-function studies using RNAi-mediated gene silencing indicated that HNF-1β facilitated GSK-3β expression, resulting in the loss of phosphorylated nuclear factor-κB (p-NFκB) and the reduction of TOV-21G cell proliferation. The cell proliferation assay also revealed that GSK-3β inhibitors rescued the effects of HNF-1β silencing on cell viability in a dose-dependent manner. Furthermore, the GSK-3β inhibitor, AR-A014418, effectively inhibited tumor cell proliferation in a xenograft mouse model. In conclusion and to the best of our knowledge, the current study was the first to determine that GSK-3β is a target gene of HNF-1β. In addition, the results of the present study revealed the novel HNF-1β-GSK-3β-p-NFκB pathway, occurring in response to DNA damage. Targeting this pathway may therefore represent a putative, novel, anticancer strategy in patients with OCCC.
博士(医学)・甲第785号・令和3年3月15日
Copyright: © Kawaharaet al. This is an open access article distributed under theterms of CreativeCommons Attribution License(https://creativecommons.org/licenses/by-nc-nd/4.0/).
identifier:Experimental and therapeutic medicine Vol.20 No.5 Article No.122 (2020 Nov)
identifier:17920981
identifier:http://ginmu.naramed-u.ac.jp/dspace/handle/10564/3909
identifier:Experimental and therapeutic medicine, 20(5): Article No.122
Persistent ID (NDL)
info:ndljp/pid/12070977
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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
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博士論文(自動収集)
Date Accepted (W3CDTF)
2022-02-06T04:33:19+09:00
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application/pdf
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