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  1. 学術雑誌論文・一般雑誌記事

Clinicopathological characteristics of thyroid transcription factor 1-negative small cell lung cancers.

https://shonan-ums.repo.nii.ac.jp/records/143
https://shonan-ums.repo.nii.ac.jp/records/143
2feedbbe-d5c3-49d2-b47a-5f8730738a19
Item type 一般雑誌記事 / Article(1)
公開日 2020-06-01
タイトル
タイトル Clinicopathological characteristics of thyroid transcription factor 1-negative small cell lung cancers.
言語 en
言語
言語 eng
キーワード
言語 en
主題Scheme Other
主題 Aged
キーワード
言語 en
主題Scheme Other
主題 Biomarkers, Tumor
キーワード
言語 en
主題Scheme Other
主題 Case-Control Studies
キーワード
言語 en
主題Scheme Other
主題 Cell Differentiation
キーワード
言語 en
主題Scheme Other
主題 Cell Proliferation
キーワード
言語 en
主題Scheme Other
主題 Female
キーワード
言語 en
主題Scheme Other
主題 Humans
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 Lung Neoplasms
キーワード
言語 en
主題Scheme Other
主題 Male
キーワード
言語 en
主題Scheme Other
主題 Middle Aged
キーワード
言語 en
主題Scheme Other
主題 Prognosis
キーワード
言語 en
主題Scheme Other
主題 Reverse Transcriptase Polymerase Chain Reaction
キーワード
言語 en
主題Scheme Other
主題 Small Cell Lung Carcinoma
キーワード
言語 en
主題Scheme Other
主題 Thyroid Nuclear Factor 1
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Iida, Yuko

× Iida, Yuko

WEKO 411

en Iida, Yuko

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Masuda, Shinobu

× Masuda, Shinobu

WEKO 412

en Masuda, Shinobu

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Nakanishi, Yoko

× Nakanishi, Yoko

WEKO 413

en Nakanishi, Yoko

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Shimizu, Tetsuo

× Shimizu, Tetsuo

WEKO 414

en Shimizu, Tetsuo

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Nishimaki, Haruna

× Nishimaki, Haruna

WEKO 415

en Nishimaki, Haruna

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Takahashi, Mai

× Takahashi, Mai

WEKO 416

en Takahashi, Mai

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Hikichi, Mari

× Hikichi, Mari

WEKO 417

en Hikichi, Mari

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Maruoka, Shuichiro

× Maruoka, Shuichiro

WEKO 418

en Maruoka, Shuichiro

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Gon, Yasuhiro

× Gon, Yasuhiro

WEKO 419

en Gon, Yasuhiro

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Takahashi, Noriaki

× Takahashi, Noriaki

WEKO 420

en Takahashi, Noriaki

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Hashimoto, Shu

× Hashimoto, Shu

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en Hashimoto, Shu

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抄録
内容記述タイプ Abstract
内容記述 Limitations in obtaining surgically resected or biopsy samples of small cell lung cancer (SCLC) tumors make comprehensive biological analyses difficult. The loss of thyroid transcription factor 1 (TTF-1) has been associated with the aggressive behavior of non-small cell lung cancer; however, clinicopathological features of TTF-1-negative SCLC remain unclear. This study aimed to elucidate the characteristics of TTF-1-negative SCLC. We studied the associations between the expression of TTF-1 and the clinicopathological factors associated with SCLC, including survival and expression of neuroendocrine markers (synaptophysin, chromogranin A, and CD56), neuroendocrine cell-specific transcription factors (ASCL1, BRN2), a proliferation marker (Ki-67 labeling index), and an oncogene (NF1B). Formalin-fixed and paraffin-embedded sections of SCLC tumors were subjected to immunohistochemistry and quantitative reverse-transcription polymerase chain reaction analyses. In a case-control cohort matched for basic clinical factors, expression of ProGRP, synaptophysin, chromogranin A, and ASCL1 was significantly decreased in TTF-1-negative SCLC samples. In contrast, there was no significant correlation between Ki-67 labeling index and TTF-1. In a larger serial case cohort, TTF-1-negative SCLC cases were older at diagnosis, but there was no significant difference in the overall survival of patients with TTF-1-negative and TTF-1-positive SCLC. In conclusion, TTF-1-negative SCLC showed decreased neuroendocrine differentiation, and significantly worse clinical outcomes were not observed.
内容記述
内容記述タイプ Other
内容記述 Limitations in obtaining surgically resected or biopsy samples of small cell lung cancer (SCLC) tumors make comprehensive biological analyses difficult. The loss of thyroid transcription factor 1 (TTF-1) has been associated with the aggressive behavior of non-small cell lung cancer; however, clinicopathological features of TTF-1-negative SCLC remain unclear. This study aimed to elucidate the characteristics of TTF-1-negative SCLC. We studied the associations between the expression of TTF-1 and the clinicopathological factors associated with SCLC, including survival and expression of neuroendocrine markers (synaptophysin, chromogranin A, and CD56), neuroendocrine cell-specific transcription factors (ASCL1, BRN2), a proliferation marker (Ki-67 labeling index), and an oncogene (NF1B). Formalin-fixed and paraffin-embedded sections of SCLC tumors were subjected to immunohistochemistry and quantitative reverse-transcription polymerase chain reaction analyses. In a case-control cohort matched for basic clinical factors, expression of ProGRP, synaptophysin, chromogranin A, and ASCL1 was significantly decreased in TTF-1-negative SCLC samples. In contrast, there was no significant correlation between Ki-67 labeling index and TTF-1. In a larger serial case cohort, TTF-1-negative SCLC cases were older at diagnosis, but there was no significant difference in the overall survival of patients with TTF-1-negative and TTF-1-positive SCLC. In conclusion, TTF-1-negative SCLC showed decreased neuroendocrine differentiation, and significantly worse clinical outcomes were not observed.
書誌情報 en : Human pathology

巻 79, p. 127-134, 発行日 2018
ISSN
収録物識別子タイプ EISSN
収録物識別子 1532-8392
PubMed番号
識別子タイプ PMID
関連識別子 29787820
DOI
識別子タイプ DOI
関連識別子 10.1016/j.humpath.2018.05.009
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