Study of metastasis-related genes in esophageal carcinoma
Study of metastasis-related genes in esophageal carcinoma
批准号:
07671315
负责人:
BABA Kinya
金额:
$1.41万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1995
资助国家:
日本
项目状态:
已结题
起止时间:
1995 至 1996
中文摘要
点击翻译按钮获取中文摘要
英文摘要
1.Study of matrix metalloproteinase 7 (MMP7)1) We performed in vitro invasion assay using squamous carcinoma cell line KY150 and its transfectant with MMP cDNA.The expression of MMP7 in parent KY150 cell was very weak. On the other hand, its expression in transfectant was increasing and determined by Northern blot analysis. The invasion assay demonstrated that the invading cells were much frequently seen in transfectants than in parent cells (56% vs 10%).2) To determine the effect of anti-MMP7 antibody, we added the antibody into the culture medium. Consequently the invading ability of KY150 transfectants was dramatically inhibited by the antibody (56%*16%).These findings support the hypothesis that MMP7 is one of the major proteinases which influence the invading ability of esophageal squamous cell carcinomas.2.Study of integrin alpha6The expression of integrin alpha6 was dramatically increased in tumor tissues rather than normal tissues of the esophagus. This was determined by Northern blot analysis and immunohistochemical analysis. The tumors showing high degree of integrin alpha6 expression were those having deeper invasion and worse prognosis. we are studying the expression level of integrin beta1 and beta4. We are also studying the correlation between integrin expression and matrix metalloproteinase (MMP7) expression because some kind of MMPs may be regulated by signal transduction relating to the integrin.
期刊论文(28)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
Ohata,M.: "The human FHIT gene,spanning the chromosome 3p14.2 fragile site and renal carcinoma associated translocation breakpoint,is abnormal in digestive tract cancers." Cell. 84. 587-597 (1996)
Ohata,M.:“跨越染色体 3p14.2 脆弱位点和肾癌相关易位断点的人类 FHIT 基因在消化道癌症中是异常的。”
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Ohta,M.: "The human FHIT gene,spanning the chromosome 3p14.2 fragile site and renal carcinoma associated translocation breakpoint,is abnormal in digestive tract cancers." Cell. 84. 587-597 (1996)
Ohta,M.:“跨越染色体 3p14.2 脆弱位点和肾癌相关易位断点的人类 FHIT 基因在消化道癌症中是异常的。”
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Mori M.et al.: "Expression of MAGE genes in human colorectal carcinoma." Ann Surg. (in press).
Mori M.等人:“MAGE 基因在人类结直肠癌中的表达”。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Mori,M.: "Expression of omithine decarboxylase mRNA in gastric cancer." Cancer. 77. 1634-1638 (1996)
Mori,M.:“胃癌中鸟氨酸脱羧酶 mRNA 的表达。”
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Mori M.et al.: "Expression of ormithine decarboxylase mRNA in gastric cancer" Cancer. (in press).
Mori M.等人:“胃癌中鸟氨酸脱羧酶 mRNA 的表达”癌症。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
共 19 条
国内基金
海外基金
登录
查看更多内容
泛素连接酶TRIM65通过RhoGAP调控Rho活性促进结直肠癌侵袭转移的分子机制
-
批准号:31970703
-
项目类别:面上项目
-
资助金额:50.0万元
-
批准年份:2019
-
负责人:陈代词
-
依托单位:
幽门螺杆菌感染促进肿瘤相关成纤维细胞与胃癌细胞的互作及机制研究
-
批准号:31760328
-
项目类别:地区科学基金项目
-
资助金额:36.0万元
-
批准年份:2017
-
负责人:周建奖
-
依托单位:
LncRNA-GMAN调控胃癌细胞侵袭和转移的分子作用机制研究
-
批准号:31771540
-
项目类别:面上项目
-
资助金额:59.0万元
-
批准年份:2017
-
负责人:卓巍
-
依托单位:
Hedgehog通路调控长链非编码RNA对胰腺癌增殖侵袭的影响及机制研究
-
批准号:81172184
-
项目类别:面上项目
-
资助金额:65.0万元
-
批准年份:2011
-
负责人:杨尹默
-
依托单位:
MDR1与Anxa2相互作用调节耐药乳腺癌细胞侵袭的分子机制研究
-
批准号:81071731
-
项目类别:面上项目
-
资助金额:31.0万元
-
批准年份:2010
-
负责人:牛瑞芳
-
依托单位:
南美蟛蜞菊入侵对土壤微生物的影响及反馈作用
-
批准号:30970556
-
项目类别:面上项目
-
资助金额:40.0万元
-
批准年份:2009
-
负责人:杜道林
-
依托单位:
与肺癌细胞侵袭相关的microRNAs研究
-
批准号:30771187
-
项目类别:面上项目
-
资助金额:30.0万元
-
批准年份:2007
-
负责人:罗泽伟
-
依托单位:
柔嫩艾美耳球虫侵入宿主细胞的分子机制
-
批准号:30500370
-
项目类别:青年科学基金项目
-
资助金额:25.0万元
-
批准年份:2005
-
负责人:李建华
-
依托单位: