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Analysis of the abnormalities of microRNA and epigenome and the clinical application in gastroenterological cancers

Analysis of the abnormalities of microRNA and epigenome and the clinical application in gastroenterological cancers
microRNA和表观基因组异常分析及其在胃肠道肿瘤中的临床应用
批准号:
23390200
负责人:
SHINOMURA Yasuhisa
金额:
$12.4万
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:
2011
资助国家:
日本
项目状态:
已结题
起止时间:
2011 至 2013

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中文摘要
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英文摘要
MicroRNAs (miRNA) constitute a class of small non-coding RNA molecules that function as post-transcriptional gene regulators. miRNAs can function as oncogenes or tumour suppressors. Therefore, they have been increasingly recognized as useful biomarkers for various human cancers. Metachronous gastric cancer (GC) can develop after endoscopic resection of GC and cannot be predicted based on clinical signature. We identified that DNA methylation of microRNA-34b/c (miR-34b/c) in the mucosa of the noncancerous gastric body may be a useful biomarker for predicting the risk of metachronous GC. With regard to colorectal cancers (CRCs), using miRNA array analysis, we recently discovered that microRNA-31 (miR-31) expression is significantly up-regulated in BRAF-mutated colorectal cancers (CRCs) compared with that in wild-type CRCs. Moreover, associations were identified between miR-31 expression, proximal tumor location and poor prognosis for CRCs. Moreover, the results of functional analysis showed that miR-31 may regulate BRAF activation and that the oncogenic role of miR-31 and its possibility of therapeutic target in CRCs. Thus, our current data suggest that miR-31 may be a diagnostic biomarker and therapeutic target in CRC. These novel data may lead to the establishment of a new therapeutic target or a theranostic procedure in gastroenterological cancers.
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会议论文
Profiling of chromatin signatures reveals epigenetic regulation of microRNA genes in colorectal cancer
染色质特征分析揭示结直肠癌中 microRNA 基因的表观遗传调控
DOI: --
发表时间: 2011
期刊: Cancer Res.
影响因子: --
作者: [Suzuki H, Takatsuka S, Akashi H, Yamamoto E, Nojima M, Maruyama R, Kai M, Yamano H, Sasaki Y, Tokino T, Shinomura Y, Imai K, Toyota M.]
通讯作者: Toyota M.
DOI: --
发表时间: 2013
期刊:
影响因子: --
作者: []
通讯作者:
大腸腫瘍におけるKRAS、BRAF、PIK3CA変異と相関を示すmicroRNAの同定を目指したアレイシステムによる網羅的検討
一项使用阵列系统的综合研究,旨在识别与结直肠肿瘤中 KRAS、BRAF 和 PIK3CA 突变相关的 microRNA
DOI: --
发表时间: 2013
期刊:
影响因子: --
作者: [Morimoto M, Numata K, Nozaki A, Kondo M, Moriya S, Taguri M, Morita S, Konno M, Sugo A, Miyajima E, Maeda S, Tanaka K, 能正 勝彦]
通讯作者: 能正 勝彦
microRNA-34b/c異常メチル化率測定による胃癌の異時性多発リスク予測
通过测量microRNA-34b/c异常甲基化率预测胃癌的异时多重风险
DOI: --
发表时间: 2013
期刊:
影响因子: --
作者: [Sawai H, Asahina Y, Tokunaga K et al, Naoyuki Sato, 鈴木 亮,山本英一郎,鈴木 拓,野島正寛,丸山玲緒,能正勝彦,山本博幸,山野泰穂,菅井 有,篠村恭久]
通讯作者: 鈴木 亮,山本英一郎,鈴木 拓,野島正寛,丸山玲緒,能正勝彦,山本博幸,山野泰穂,菅井 有,篠村恭久
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