Cell lineage-related mechanisms involved in lung cancer stem cell development.
Cell lineage-related mechanisms involved in lung cancer stem cell development.
批准号:
23501281
负责人:
OSADA Hirotaka
金额:
$3.08万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2011
资助国家:
日本
项目状态:
已结题
起止时间:
2011 至 2013
中文摘要
最初从几种不同的肺癌细胞系中建立了球体形成细胞,之后表达谱和肿瘤发生测定结果表明它们具有癌症干细胞特性。此外,这些细胞中神经内分泌相关基因的表达表明球体形成和细胞谱系可塑性之间可能存在关联。此外,神经内分泌诱导的ASH1也被发现在一些细胞系中促进球体形成,这表明ASH1信号转导参与了癌症干细胞的发育。
英文摘要
Sphere-forming cells were initially established from several different lung cancer cell lines, after which expression profiling and tumorigenesis assay findings indicated their cancer stem cell properties. In addition, expression of neuroendocrine-related genes in these cells suggests a possible association between sphere formation and cell lineage plasticity. Furthermore, neuroendocrine-inducing ASH1 has also been found to promote sphere formation in some cell lines, suggesting the involvement of ASH1 signaling in development of cancer stem cells.
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The circadian clock gene BMAL1 is a novel therapeutic target for malignant mesothelioma
生物钟基因BMAL1是恶性间皮瘤的新治疗靶点
DOI:
--
发表时间:
2012
期刊:
Int J Cancer
影响因子:
6.4
作者:
[Elshazley M, Sato M, Hase T, Takeyama Y, Yamashita R, Yoshida K, Toyokuni S, Ishiguro F, Osada H, Sekido Y, Yokoi K, Usami N, Shames DS, Kondo M, Gazdar AF, Minna JD, Hasegawa Y]
通讯作者:
Hasegawa Y
miR-375 is activated by ASH1 and inhibits YAP1 in a lineage dependent manner in lung cancermiR-375 is activated by ASH1 and inhibits YAP1 in a lineage dependent manner in lung cancer
在肺癌中,miR-375 被 ASH1 激活,并以谱系依赖性方式抑制 YAP1 在肺癌中,miR-375 被 ASH1 激活,并以谱系依赖性方式抑制 YAP1
DOI:
--
发表时间:
2011
期刊:
Cancer Res
影响因子:
11.2
作者:
[Nishikawa E, Osada H, Okazaki Y, Arima C, Tomida S, Tatematsu Y, Taguchi A, Shimada Y, Yanagisawa K, Yatabe Y, Toyokuni S, Sekido Y, Takahashi T]
通讯作者:
Takahashi T
Epithelial to mesenchymal transition in an EGFR-mutant lung cancer cell line with acquired resistance to erlotinib
对厄洛替尼获得性耐药的 EGFR 突变肺癌细胞系的上皮细胞向间质细胞转变
DOI:
--
发表时间:
2011
期刊:
J Thorac Oncol
影响因子:
20.4
作者:
[Suda K, Tomizawa K, Fujii M, Murakami H, Osada H, Maehara Y, Yatabe Y, Sekido Y, Mitsudomi T]
通讯作者:
Mitsudomi T
Overexpression of activated leukocyte cell adhesion molecule is involved in invasion of malignant mesothelioma cells
活化白细胞粘附分子过度表达参与恶性间皮瘤细胞侵袭
DOI:
--
发表时间:
2011
期刊:
影响因子:
--
作者:
[野村 幸世, 愛甲 丞, 大本 安一, 多田 稔, 大津 洋, 三浦 洋菜, 山形 幸徳, 瀬戸 泰之, 上西 紀夫, Mizuno T, 野村 幸世, Ishiguro F]
通讯作者:
Ishiguro F
YAP transcription coactivator induces malignant mesothelioma cell proliferation by up-regulating cell cycle progression
YAP转录共激活剂通过上调细胞周期进程诱导恶性间皮瘤细胞增殖
DOI:
--
发表时间:
2011
期刊:
影响因子:
--
作者:
[Osada H, Takahashi T, 野村 幸世, Osada H, Mizuno T]
通讯作者:
Mizuno T
共 37 条
Investigation of epigenetic abnormalities involved in lung cancer progression.
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财政年份:2004
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The mechanism of apoptosis induction by TGF-β stimuli and its clinical application
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.24万
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财政年份:2001
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负责人:OSADA Hirotaka
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依托单位:
Involvement of LIM domain proteins and Lbd2 in the lung tissue development and carcinogensis.
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批准号:11670158
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.11万
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财政年份:1999
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负责人:OSADA Hirotaka
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依托单位:
Functional Characterization of LIMK2 carrying LIM and PDZ Domains in the Developmental and Tumorigenic Process.
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负责人:OSADA Hirotaka
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依托单位:
海外基金