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Subcellular localization of hTERT in breast cancer:insights into its tumorigenesis and drug resistance mechanisms in HER2-immunopositive breast cancer

https://asahikawa-med.repo.nii.ac.jp/records/2000319
https://asahikawa-med.repo.nii.ac.jp/records/2000319
62e8e522-b1ad-42ed-b919-eacf078954d3
名前 / ファイル ライセンス アクション
K591 K591 Uno Yuji_TD.pdf (4.3 MB)
Item type 学位論文 / Thesis or Dissertation_02(1)
公開日 2025-02-10
タイトル
タイトル Subcellular localization of hTERT in breast cancer:insights into its tumorigenesis and drug resistance mechanisms in HER2-immunopositive breast cancer
言語 en
言語
言語 eng
キーワード
言語 en
主題Scheme Other
主題 Breast cancer
キーワード
言語 en
主題Scheme Other
主題 Drug resistance
キーワード
言語 en
主題Scheme Other
主題 Human telomerase reverse transcriptase
キーワード
言語 en
主題Scheme Other
主題 Immunohistochemistry
キーワード
言語 en
主題Scheme Other
主題 Intracellular localization
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_db06
資源タイプ doctoral thesis
アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
その他(別言語等)のタイトル
その他のタイトル 乳癌におけるhTERTの細胞内局在の検討:HER2陽性乳癌における腫瘍形成と薬剤耐性メカニズムへの関与
言語 ja
著者 鵜野, 裕治

× 鵜野, 裕治

ja 鵜野, 裕治

ja-Kana ウノ, ユウジ

en Uno, Yuji

Search repository
bibliographic_information en : Hunan Pathology

巻 134, p. 74-84, 発行日 2023-04-01
ISSN
収録物識別子タイプ PISSN
収録物識別子 0046-8177
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 https://doi.org/10.1016/j.humpath.2022.12.010
識別番号 その他
内容記述タイプ Other
内容記述 PMID:36549600
言語 en
dissertation_number
学位授与番号 甲第591号
学位授与年月日
学位授与年月日 2023-06-30
学位名
言語 ja
学位名 博士(医学)
item_10_degree_grantor_32
言語 ja
学位授与機関名 旭川医科大学
item_10_description_33
内容記述タイプ Abstract
内容記述 Human telomerase reverse transcriptase (hTERT) is highly expressed in various cancers, including breast cancer. Although telomere elongation is an essential role for hTERT, the nuclear export after oxdative stress has also been shown in several cancer cell lines and is associated with drug-resistance in vitro. As only a few reports focused on the subcellular localization of hTERT in clinical specimens, we performed immunohistochemistry (IHC) and analyzed the correlation between intracellular hTERT expression and the clinicopathological characteristics to identify the clinical significance of hTERT subcellular expression in breast cancers. 144 invasive breast cancers classified by IHC subtype without primary systemic therapy (PST), were selected from a surgical resection cohort and were immunostained for hTERT, p-STAT3, p-AKT and p-ERK. The nuclear and/or cytoplasmic staining intensity and proportion of hTERT were scored and compared with clinicopathological parameters. The nuclear hTERT expression was significantly correlated with HER2 expression (p = 0.00156), and the scores were significantly correlated with p-STAT3 and p-AKT expression scores (r = 0.532, p = 0.000587 and r = 0.345, p = 0.0339, respectively) in the HER2-immunopositive breast cancer including luminal-HER2 and HER2 subtypes. Furthermore, hTERT was expressed more in cytoplasm in the specimens after PST than those before PST, and the score tended to be negatively correlated with tumor shrinkage rate in HER2 subtype (r = -0.593, p = 0.0705). These results suggest that nuclear and/or cytoplasmic hTERT may play a different role before and after PST including the tumorigenesis and drug-resistance in breast cancer. Suppression of cytoplasmic hTERT expression may lead to more effective strategy for drug-resistant HER2 subtype in breast cancer.
言語 en
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
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鵜野, 裕治, n.d., Subcellular localization of hTERT in breast cancer:insights into its tumorigenesis and drug resistance mechanisms in HER2-immunopositive breast cancer: 74–84 p.

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