Studies for NACC1,a pluripotent transcriptional factor, in tumorcells
Studies for NACC1,a pluripotent transcriptional factor, in tumorcells
批准号:
22390071
负责人:
MAESAWA Chihaya
金额:
$11.9万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2010
资助国家:
日本
项目状态:
已结题
起止时间:
2010 至 2012
中文摘要
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英文摘要
NACC1 is a member of pluripotent transcription factor, and associates with malignant phenotypes of tumor cells. The present study investigated the molecular mechanisms of NACC1 in malignant tumors. We represented that NACC1 directly bound to HDAC6, and deacetylated tubulin and cortactin. This deacetylation introduced acceleration of motility and invasion of tumor cells. NACC1 also contributed to stabilization of ERBB2 protein expression through the deacetylation of HSP90. The SUMOlylation of NACC1 introduced the binding with PML protein. Our study demonstrated that overexpression of NACC1 protein contributes to motility, invasion, proliferation activities of tumor cells, and may be a good candidate for molecular target medicine in cancer therapy.
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NACC1蛋白質のSUMO化はPML nuclear bodyへの取り込みに関連している(NACC1 recruitment within the PML nuclear body is mediated by covalent and non-covalent binding through SUMO modification)(英語).
NACC1 蛋白的 SUMO 化与其进入 PML 核体的摄取相关(NACC1 在 PML 核体内的募集是通过 SUMO 修饰通过共价和非共价结合介导的)。
DOI:
--
发表时间:
2010
期刊:
影响因子:
--
作者:
[前沢 千早, 舘道 芳徳, 及川 浩樹, 増田 友之]
通讯作者:
増田 友之
Different susceptibility to insulin resistance and fatty liver depending on the combination of TNF-alpha C-857T and adiponectin G+276T gene polymorphisms in Japanese subjects with type 2 diabetes
日本 2 型糖尿病受试者对胰岛素抵抗和脂肪肝的易感性不同,取决于 TNF-α C-857T 和脂联素 G 276T 基因多态性的组合
DOI:
--
发表时间:
2012
期刊:
Tohoku J Exp Med
影响因子:
2.2
作者:
[Sasaki M, Matsubara T, Yoneda N, Nomoto K, Tsuneyama K, Sato Y, Nakanuma Y, 上原郁野, 中尾光善 監修, Ohara M]
通讯作者:
Ohara M
悪性黒色腫細胞株の網羅的エクソーム解析による新規原因遺伝子の解析
通过恶性黑色素瘤细胞系的综合外显子组分析来分析新的致病基因
DOI:
--
发表时间:
2012
期刊:
影响因子:
--
作者:
[Matsubara T, Sato Y, Sasaki M, Harada K, Nomoto K, Tsuneyama K, Nakanuma Y, 三浦 慎平]
通讯作者:
三浦 慎平
Sensor and effector kinases in DNAdamage checkpoint regulate capacity for homologous recombination repair offission yeast in G2 phase.
DNA 损伤检查点中的传感器和效应激酶调节 G2 期同源重组修复裂殖酵母的能力。
DOI:
10.1016/j.dnarep.2012.05.006
发表时间:
2012
期刊:
DNA Repair (Amst).
影响因子:
--
作者:
[Yasuhira S, Saito T, Maesawa C, Masuda T.]
通讯作者:
Masuda T.
NACC1/HDAC6脱アセチル化機構はアクチンおよび微小間依存性の腫瘍細胞の運動能に影響を与える(NACC1/HDAC6 deacetylation system accelerates tumor cell migration via an actin - andmicrotubule-dependent process)(英語).
NACC1/HDAC6 脱乙酰化系统通过肌动蛋白和微管依赖性过程加速肿瘤细胞迁移。
DOI:
--
发表时间:
2011
期刊:
影响因子:
--
作者:
[前沢千早,多田広志,角田加奈子,柴崎晶彦,安平進士,及川弘樹,管野公徳,石川雄一,増田友之]
通讯作者:
前沢千早,多田広志,角田加奈子,柴崎晶彦,安平進士,及川弘樹,管野公徳,石川雄一,増田友之
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Development of high resolution imaging for tumor boundary delineation using 7-tesla magnetic resonance imaging enhanced by high iron diamine immersion
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批准号:24659283
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项目类别:Grant-in-Aid for Challenging Exploratory Research
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资助金额:$2.25万
-
财政年份:2012
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负责人:MAESAWA Chihaya
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依托单位:
Alterations of microRNA associated with cancer-related genes
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批准号:19590363
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.91万
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财政年份:2007
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负责人:MAESAWA Chihaya
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依托单位:
Significance of maspin tumor suppressor genes in human tumors
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批准号:16590290
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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:2004
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负责人:MAESAWA Chihaya
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依托单位:
海外基金