Biological role of genes at genetic alteration regions for proliferation and differentiation in hem
Biological role of genes at genetic alteration regions for proliferation and differentiation in hem
批准号:
18390286
负责人:
SETO Masao
金额:
$11.23万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2006
资助国家:
日本
项目状态:
已结题
起止时间:
2006 至 2007
中文摘要
点击翻译按钮获取中文摘要
英文摘要
1. Adult T-cell leukemia/lymphoma : Array CGH analysis revealed that genome profiles of acute and lymphoma types are distinct, and suggested that ATLL genetic alterations after HTLV1 infection may play a role for oncogenesis of the two clinmically distinct disease subtypes. Further characterization of genomic regions and identification of responsible genes from these regions are warranted. This will reveal functional significance of these genes in cell profilferation and differentiations.2. T/NK leukemia/lymphoma : extranodal T/NK and Aggressive NK lymphomas were found to have distinct genetic alteration patterns although clinical manifestations and EBV involvement are similar.3. Peripheral T-cell lymphoma-unspecified(PTCL-U) : PTCL-U with multiple genomic alterations were found in about half of the cases and the pattern of genomic alterations are similar to that of ATLL lymphoma type. Histology also showed similarity in that they have peomorphic nuclear shape and CCR4 expression.4. B-cell lymphoma : We have identified BIM gene loss in mantle cell lymphoma(MCL) . BIM gene is known to regulate BCL2 function. We therefore examined significance of apoptotic gene family by expression profiling analysis and suggested that a poor prognosis group in the MCL exist. This needs to further confirmation.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
Isoform-specific potentiation of stem and progenitor cell engraftment by AML1/RUNX1.
AML1/RUNX1对茎和祖细胞植入的同工型特异性增强。
DOI:
10.1371/journal.pmed.0040172
发表时间:
2007-05
期刊:
PLoS medicine
影响因子:
15.8
作者:
[Tsuzuki S, Hong D, Gupta R, Matsuo K, Seto M, Enver T]
通讯作者:
Enver T
Comparison of PTCL-U and lymphoma-type ATLL in terms of genomic imbalance by using array CGH analysis.
使用阵列 CGH 分析比较 PTCL-U 和淋巴瘤型 ATLL 的基因组失衡。
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[Tsuzuki, S., 中川 雅夫]
通讯作者:
中川 雅夫
Karnan S.,Tagawa,H.,Masao Seto:Ocular adnexal marginal zone B cell lymphoma showed distinct genomic profile.
Karnan S.,Takawa,H.,Masao Seto:眼附件边缘区 B 细胞淋巴瘤表现出独特的基因组谱。
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[Honma, K.]
通讯作者:
K.
Ocular adnexal marginal zone B cell lymphoma has characteristic deletion at chromosome band 6q23.3-24.1 whose target is TNFAIP3.
眼附件边缘区B细胞淋巴瘤在染色体带6q23.3-24.1处有特征性缺失,其靶点是TNFAIP3。
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[Honma, K.]
通讯作者:
K.
Array-based comparative genomic hybridization(array-CGH)法を用いた胃癌における網羅的な染色体構造異常の解析.
采用基于芯片的比较基因组杂交(array-CGH)方法对胃癌染色体结构异常进行综合分析。
DOI:
--
发表时间:
2006
期刊:
影响因子:
--
作者:
[Oshiro, A., 瀬戸 加大, 都築 忍, 横山 俊彦, 内田 智久]
通讯作者:
内田 智久
共 59 条
Lymphomagenesis pathway consisting of various cooperative genes and their relevance as molecular target therapy
-
批准号:24390249
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$10.73万
-
财政年份:2012
-
负责人:SETO Masao
-
依托单位:
Establishment of functional analysis for genes involved in NK cell tumors using normal NK cell expansion method
-
批准号:23659194
-
项目类别:Grant-in-Aid for Challenging Exploratory Research
-
资助金额:$2.5万
-
财政年份:2011
-
负责人:SETO Masao
-
依托单位:
Biologic significance of candidate genes in genomic alteration regions of lymphoidmalignancies
-
批准号:20390277
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$11.98万
-
财政年份:2008
-
负责人:SETO Masao
-
依托单位:
Molecular mechanisms of lymphomagenesis
-
批准号:17015050
-
项目类别:Grant-in-Aid for Scientific Research on Priority Areas
-
资助金额:$54.21万
-
财政年份:2005
-
负责人:SETO Masao
-
依托单位:
Genomic alteration in hematologic malignancies and their roles for proliferation and differentiation
-
批准号:16390282
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$9.15万
-
财政年份:2004
-
负责人:SETO Masao
-
依托单位:
Roles of translocation junction genes for proliferation and differentiation of hemotolymphoid cell
-
批准号:14370312
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$8.9万
-
财政年份:2002
-
负责人:SETO Masao
-
依托单位:
Chromosome translocation junction genes on lympho-hematopoietic cell proliferation and differentiation
-
批准号:11470215
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$9.34万
-
财政年份:1999
-
负责人:SETO Masao
-
依托单位:
BIOLOGICAL ROLE OF CHROMOSOME TRANSLOCATION JUNCTION REGION GENES IN HEMATOPOIETIC CELL DIFFERENTIATION AND PROLIFERATION
-
批准号:08457282
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$5.18万
-
财政年份:1996
-
负责人:SETO Masao
-
依托单位:
国内基金
海外基金
登录
查看更多内容
铜调控调节性 T 细胞在类风湿性关节炎的功能机制研究
-
批准号:ZCLJHSQY26H0601
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:常杰
-
依托单位:
基于CD99靶点CAR-T产品治疗T-ALL/AML的安全性与有效性研究
-
批准号:JCZRLH202600888
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:
-
依托单位:
梅毒螺旋体外膜蛋白Tp92经由宿主膜蛋白互作调控MYC诱导CD4⁺ T细胞衰老的分子机制
-
批准号:2026JJ60545
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:刘兆平
-
依托单位:
CD161-CLEC2D轴通过BATF/IRF5抑制骨髓驻留记忆CD8+T细胞抗多发性骨髓瘤功能的机制研究
-
批准号:2026JJ30149
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:李昕
-
依托单位:
高效Mage转座系统赋能KRAS G12D突变结直肠癌新型TCR-T疗法开发临床前研究
-
批准号:JCZRQNB202600936
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:
-
依托单位:
靶向抑制HDAC6介导STAT1乙酰化修饰调控cDC2-CD4+T细胞互作缓解肠道炎症的机制研究
-
批准号:2026JJ81338
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:艾飞艳
-
依托单位:
靶向Gal-1提高肝内胆管癌T细胞功能及增敏PD-1免疫治疗的机制研究
-
批准号:2026JJ81642
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:李浩
-
依托单位:
Domain理论中几类T0拓扑空间的幂构造研究
-
批准号:2026JJ81209
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:袁珍珠
-
依托单位:
介入输注CRISPR-Cas9 构建的 SHP-1-KO T 细胞联合靶向肝癌细胞脂质代谢通路的协同抗肝癌机制研究
-
批准号:2026JJ50324
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:刘华平
-
依托单位:
下瘀血汤调控肿瘤驻留菌-琥珀酸信号轴重塑CD8+T细胞免疫表型的抗肝癌机制研究
-
批准号:2026JJ50326
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:谭年花
-
依托单位: