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Carbon Ion Beam Combined with Gemcitabine Remarkably Disrupts Pancreatic Cancer Stem-Like Cells via Complex DNA Double Strand Breaks (DSBs) and Multiple Cell Death Pathways

https://repo.qst.go.jp/records/71759
https://repo.qst.go.jp/records/71759
12829813-1ebe-4fb0-b7e2-3c31f4512b9b
Item type 会議発表用資料 / Presentation(1)
公開日 2015-06-30
タイトル
タイトル Carbon Ion Beam Combined with Gemcitabine Remarkably Disrupts Pancreatic Cancer Stem-Like Cells via Complex DNA Double Strand Breaks (DSBs) and Multiple Cell Death Pathways
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_c94f
資源タイプ conference object
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 Sai, Sei

× Sai, Sei

WEKO 706318

Sai, Sei

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Shirai, Toshiyuki

× Shirai, Toshiyuki

WEKO 706319

Shirai, Toshiyuki

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崔 星

× 崔 星

WEKO 706320

en 崔 星

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白井 敏之

× 白井 敏之

WEKO 706321

en 白井 敏之

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抄録
内容記述タイプ Abstract
内容記述 Purpose
To elucidate whether carbon ion beam alone or in combination with gemcitabine has advantages over X-ray irradiation in targeting putative human pancreatic cancer stem cells (CSCs).
Materials and Methods
Human pancreatic CSCs sorted from PANC1 and PK45 cells were treated with carbon ion beam, X-ray alone or in combination with gemcitabine, and then colony, spheroid and tumor formation assays, RT Profiler PCR Array assay, immunofluorescence γH2AX foci assay as well as in vivo tumor control analysis were performed.
Results
The colony, spheroid formation as well as tumorigenicity assays confirmed that CD44+/ESA+ cells exactly have CSC properties compared to CD44-/ESA- cells. CSCs were more highly enriched after X-ray or gemcitabine compared to carbon ion beam alone, but extremely enhanced either X-ray or carbon ion beam in combination with gemcitabine. The number of colony and spheroid formed from CSCs after carbon ion beam was significantly reduced compared to that of X-ray, and it was extremely suppressed when combined with gemcitabine. The relative biological effectiveness (RBE) values for the carbon ion beam relative to X-ray at the D10 levels for CSCs were 2.13-2.78. RT Profiler PCR Array analysis showed that expressions of apoptosis-related genes (Bax, Cytochrome c), autophagy-related genes (LC3, p62), and senescence-related gene p21 were remarkably induced after carbon ion beam combined with gemcitabine compared to carbon ion beam alone or X-ray combined with gemcitabine. Immunofluorescence assay showed that not only the number but also the size of γH2AX foci in CSCs were lager 24 h after carbon ion beam combined with gemcitabine compared to carbon ion beam alone or X-ray combined with gemcitabine. Xenograft tumor control analysis showed that the tumors were not completely controlled even treated with 60 Gy of X-ray, but it was destroyed with 25 Gy of carbon ion beam combined with 50 mg/kg gemcitabine.
Conclusions
Carbon ion beam combined with gemcitabine has superior potential to kill pancreatic CSCs via unrepairable clustered DSB, and multiple cell death pathways at relatively lower doses compared to carbon ion alone or X-ray combined with gemcitabine.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 Combined EPC & IAP Meeting 2014
発表年月日
日付 2014-06-27
日付タイプ Issued
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