EVALUATION OF GRANDE OF MALLIGNANCY ON THE BASIS OF CELL CYCLE ADHESION MOLECULESIN ORAL SQUAMOUS CELL CARCUNOMA
EVALUATION OF GRANDE OF MALLIGNANCY ON THE BASIS OF CELL CYCLE ADHESION MOLECULESIN ORAL SQUAMOUS CELL CARCUNOMA
批准号:
18592222
负责人:
YAMAGUCHI Akira
金额:
$2.26万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
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
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英文摘要
Dysregulation of tumor suppressor gene p53 has been shown to play a significant role in development of a wide variety of human malignancies. Some investigators have suggested that accumulated expression of p53 gene protein is useful as a prognostic indicator in oral squamous cell carcinoma (OSCC), although others have reported conflicting result. The aim of this study is to determine the correlation between the expression of p53 gene protein and the clinicopathological features of 140 OSCC. Tumor biopsies obtained from patients with OSCC were examined for the immunohistochemical detection of p53 gene product with special reference to expression pattern correlated with clinicopathological findings and overall survival. Nuclear accumulation of p53 was visualized as marginal pattern, dispersed pattern, or mixed pattern. Simple evaluation of p53 expression (negative and positive) defined with value of 10% did not provide useful information as to the assessment of oral.cancer However, dispe … More rsed type p53 protein expression significantly correlated with nodal metastasis, differentiation of tumor cell, overall survival and mutation. These finding suggest that p53 expression may, but not p53 positivity, be one of biological makers for the degree of malignancy in OSCC.Genetic and epigenetic alterations in tumor-suppressor genes play important roles in human neoplasia. Ras signaling is often activated in OSCC, although RAS mutations are rarely detected in OSCC patients. In present study, we examined the expression and and methylation statuses of RAS association family (RASSF) genes in OSCC. We frequently detected methlaion of RASSF1 (7/17:41.2%) RASSF2 (12/17:70.6%), RASSF5 (4/17:23.5%) in a panel of OSCC cell lines, as well as in specimens collected from 46 OSCC patient (RASSF1, 6/46, 13.0%; RAsSF2,12/46, 26.1%; RASSF5,5/46,10.9%). Our findings indicate that epigenetic inactivation of RASSF plays a key role in OSCC tumorigenesis, and that RASSF may be an important molecular target for the diagnosis and treatment of OSCC. Less
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舌癌の郭清範囲に関する検討
舌癌切除范围的思考
DOI:
--
发表时间:
2006
期刊:
頭頸部癌 34(4)
影响因子:
--
作者:
[Ueda, G., Sunakawa, H., Nakamori, K., Shinya, T., Tsuhako, W., Tamura, Y., Kosugi, T., Sato, N., Ogi, K., Hiratsuka, H, Ueda G, 仲盛健治, 仲盛健治]
通讯作者:
仲盛健治
IFN-γ induces Q2 NK-mediated antitumor effects against oral aquamous cell carcinoma cells
IFN-γ诱导 Q2 NK 介导的针对口腔水癌细胞的抗肿瘤作用
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[仲盛健司, 宮崎晃亘他, 小林 淳一, 山本 崇, Yamaguchi A, Tomihara K]
通讯作者:
Tomihara K
口腔癌に対するIFAとIFN-αを併用したsurvivinペプチドワクチンの第一相臨床試験
联合IFA和IFN-α对抗口腔癌的survivin肽疫苗一期临床试验
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[Yamaguchi, A, 宮崎 晃亘, 宮崎 晃亘]
通讯作者:
宮崎 晃亘
RAS関連遺伝子のジェネティックおよびエピジェネティックな異常の解析
RAS相关基因的遗传和表观遗传异常分析
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[Miyazaki, A, Imai T, Yamamoto T, Miyazaki A, 今井 崇, 仲盛 健治, 今井 崇]
通讯作者:
今井 崇
HLA-A24拘束性自家口腔扁平上癌障害性T細胞の解析
HLA-A24 限制性自体口腔鳞癌毒性 T 细胞分析
DOI:
--
发表时间:
2006
期刊:
影响因子:
--
作者:
[Dehari, H, 宮崎 晃亘, 仲盛 健治, 宮崎 晃亘, 山本 崇, 今井 崇, 仲盛 健治, 山本 崇, 小林 淳一, 今井 崇, 今井 崇, 小林 淳一]
通讯作者:
小林 淳一
共 33 条
Fundamental research of practical use of Super Fine Silica Powder Slurry Materials for countermeasure against liquefaction
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批准号:26420485
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项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$2.83万
-
财政年份:2014
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负责人:YAMAGUCHI Akira
-
依托单位:
Involvement in alpha-synuclein function and pathology in lysosomal storage diseases
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批准号:25460500
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.24万
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财政年份:2013
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负责人:YAMAGUCHI Akira
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依托单位:
Development of micro-SQUID-NMR for low temperature condensed matter physics
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批准号:24654109
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项目类别:Grant-in-Aid for Challenging Exploratory Research
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资助金额:$2.5万
-
财政年份:2012
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负责人:YAMAGUCHI Akira
-
依托单位:
Elucidation of the mechanisms underlying in the immunological abnormalities of lysosomal storage diseases
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批准号:23790448
-
项目类别:Grant-in-Aid for Young Scientists (B)
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资助金额:$2.83万
-
财政年份:2011
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负责人:YAMAGUCHI Akira
-
依托单位:
Challenge to clarify the acquirement of osteonetwork
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批准号:23659854
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项目类别:Grant-in-Aid for Challenging Exploratory Research
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资助金额:$2.33万
-
财政年份:2011
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负责人:YAMAGUCHI Akira
-
依托单位:
Maintenance and disturbance of osteonetwork: basic studies on clarification of pathophysiology of craniofacial bone diseases
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批准号:22249061
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项目类别:Grant-in-Aid for Scientific Research (A)
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资助金额:$30.78万
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财政年份:2010
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负责人:YAMAGUCHI Akira
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依托单位:
Spin current manipulation for highly spin-polarized superfluid helium-3
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批准号:22684019
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项目类别:Grant-in-Aid for Young Scientists (A)
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资助金额:$17.31万
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财政年份:2010
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负责人:YAMAGUCHI Akira
-
依托单位:
Chip chiral separation based on specific molecular transport inside nanofluidic channel
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批准号:21685009
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项目类别:Grant-in-Aid for Young Scientists (A)
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资助金额:$17.47万
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财政年份:2009
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负责人:YAMAGUCHI Akira
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依托单位:
Direct observation of dynamics on nanoscale magnets: Development of SQUID magnetometers
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批准号:20684015
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项目类别:Grant-in-Aid for Young Scientists (A)
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资助金额:$16.14万
-
财政年份:2008
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负责人:YAMAGUCHI Akira
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依托单位:
Layered Bayes Model and Information Criteria for Rare Event Risk Analysis
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批准号:20560775
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项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$2.08万
-
财政年份:2008
-
负责人:YAMAGUCHI Akira
-
依托单位:
Crosstalk among cells and molecules during bone regeneration
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批准号:19209057
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项目类别:Grant-in-Aid for Scientific Research (A)
-
资助金额:$31.78万
-
财政年份:2007
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负责人:YAMAGUCHI Akira
-
依托单位:
High temperature metamorphism on planetesimals and protoplanetary crust
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批准号:19540511
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项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$2.66万
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财政年份:2007
-
负责人:YAMAGUCHI Akira
-
依托单位:
Autoantibody dependent inflammatory response is a new therapeutic target for the GM2 gangliosidoses
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批准号:19790734
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项目类别:Grant-in-Aid for Young Scientists (B)
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资助金额:$2.34万
-
财政年份:2007
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负责人:YAMAGUCHI Akira
-
依托单位:
Study of Resistive Plate Chamber with high rate capability
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批准号:15540246
-
项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.86万
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财政年份:2003
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负责人:YAMAGUCHI Akira
-
依托单位:
Comprehensive analysis of bone formation and its application
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批准号:14104015
-
项目类别:Grant-in-Aid for Scientific Research (S)
-
资助金额:$72.47万
-
财政年份:2002
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负责人:YAMAGUCHI Akira
-
依托单位:
DEVELOPMENT OF A NEW THERAPEUTC APPROCH TO BONE REGENERATION FOR GENE THERAPY
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批准号:12557153
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$8.51万
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财政年份:2000
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负责人:YAMAGUCHI Akira
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依托单位:
Development of a therapeutic method of bone repair using BMP responding mesencbymal cells
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批准号:09557140
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$5.95万
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财政年份:1997
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负责人:YAMAGUCHI Akira
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依托单位:
Multivariate analysis of chemotherapeutic effect for oral cancer by tumor markers
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批准号:09470459
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$4.03万
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财政年份:1997
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负责人:YAMAGUCHI Akira
-
依托单位:
Morphological and molecular analyses of bone repair
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批准号:09470395
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$8.38万
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财政年份:1997
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负责人:YAMAGUCHI Akira
-
依托单位:
Role of BMP in fracture repair
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批准号:07457432
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项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$4.61万
-
财政年份:1995
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负责人:YAMAGUCHI Akira
-
依托单位:
海外基金