Study of expression mechanism of laminin-5 γ2 chain in colon cancer cell lines
Study of expression mechanism of laminin-5 γ2 chain in colon cancer cell lines
批准号:
15591440
负责人:
MASAKI Tadahiko
金额:
$1.79万
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:
2003
资助国家:
日本
项目状态:
已结题
起止时间:
2003 至 2005
中文摘要
MMP-7和层粘连蛋白-5 γ2链在癌细胞系中的表达(1)在L-10和HT-29细胞中,MMP-7和层粘连蛋白-5 γ2链均在癌细胞的细胞质中表达,而在SW 620、Colo 320 D、LS 174 T细胞中,这些蛋白不表达。队列迁移模型(2)如Nabeshima等人所建议的,队列迁移模型实际上在L-10细胞中观察到,然而,在所检查的其它细胞系中未观察到。L-10细胞在组织培养载玻片上形成相互连接、堆积的细胞岛,部分癌细胞从细胞岛向外迁移到岛间空间,形成一个细胞厚的连贯细胞片。HGF/SF刺激实验(3)重组肝细胞生长因子/分散因子(HGF/SF)刺激L-10细胞后,L-10细胞迁移数明显增加,抑制实验(4)L-10细胞在抗hMMP-7(+)培养液中培养时,MMP-7和LN-5 γ2链均表达于细胞浆中,MMP-7和LN-5 γ2链表达于细胞浆中。以与在普通培养基中培养时相同的方式观察到群体迁移。MMP-7和LN-5 γ2链的表达模式也相似。
英文摘要
MMP-7 and laminin-5 γ2 chain expression in cancer cell lines(1) In L-10 and HT-29 cells, both MMP-7 and laminin-5 γ2 chain were expressed in the cytoplasm of cancer cells, whereas in SW620, Colo320D, LS174T cells these proteins were not expressed.Cohort migration model(2) As Nabeshima et al.suggested, cohort migration model was actually observed in L-10 cells, however, it was not observed in the other cell lines examined. L-10 cells formed interlinked, piled-up cell islands on the tissue culture glass slides, and some cancer cells migrated outward from the cell islands into inter-island spaces as coherent cell sheets with one-cell thick. Both MMP-7 and laminin-5 γ2 chain were expressed in the cytoplasm of migrated cancer cellsHGF/SF stimulation test(3) When stimulated with recombinant hepatocyte growth factor/scattered factor (HGF/SF), the number of migrated L-10 cells were significantly increased as compared with that without stimulation.Suppression test(4) When L-10 cells were cultured in the anti-h MMP-7 (+) medium, cohort migration was observed as in the same fashion as when cultured in the ordinary medium. The expression patterns of MMP-7 and laminin-5 γ2 chain were also similar.
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Masaki T, et al.: "Matrix metalloproteinases may contribute compensationally to tumor invasion in T1 colorectal carcinomas"Anticancer Res. 23(5B). 4169-4174 (2003)
Masaki T 等人:“基质金属蛋白酶可能对 T1 结直肠癌的肿瘤侵袭作出补偿性贡献”Anticancer Res。
DOI:
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作者:
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通讯作者:
Matrix metalloproteinases may contribute compensationally to tumor invasion in T1 colorectal carcinomas.
基质金属蛋白酶可能补偿性地促进 T1 期结直肠癌的肿瘤侵袭。
DOI:
--
发表时间:
2003
期刊:
Anticancer Res. 23(5b)
影响因子:
--
作者:
[Masaki T, Sugiyama M, Matsuoka H, Abe N, Izumisato Y, Sakamoto A, Atomi Y.]
通讯作者:
Atomi Y.
DOI:
10.1002/jso.20369
发表时间:
2005-10-01
期刊:
JOURNAL OF SURGICAL ONCOLOGY
影响因子:
2.5
作者:
[Masaki, T, Matsuoka, H, Atomi, Y]
通讯作者:
Atomi, Y
Masaki T, et al.: "Coexpression of Matrilysin and laminin-5 γ2 chain may contribute to tumor cell migration in colorectal carcinomas"Dig Dis Sci. 48(7). 1262-1267 (2003)
Masaki T 等人:“Matrilysin 和层粘连蛋白 5 γ2 链的共表达可能有助于结直肠癌中的肿瘤细胞迁移”Dig Dis Sci. 1262-1267 (2003)。
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大腸疾患now2005
现在的结肠病2005年
DOI:
--
发表时间:
2005
期刊:
影响因子:
--
作者:
[正木忠彦, 松岡弘芳, 阿部展次, 他]
通讯作者:
他
Atomic dynamics in the solidification process from the undercooled liquid state
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批准号:19360346
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$10.4万
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财政年份:2007
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负责人:MASAKI Tadahiko
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依托单位:
Association between prognosis and LOH in colorectal cancers
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批准号:07671366
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.47万
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财政年份:1995
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负责人:MASAKI Tadahiko
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依托单位:
Analysis of the T-cells for the specific adoptive immunotherapy.
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批准号:03670613
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项目类别:Grant-in-Aid for General Scientific Research (C)
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资助金额:$1.34万
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财政年份:1991
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负责人:MASAKI Tadahiko
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依托单位:
国内基金
海外基金
Missing in Metastasis基因在子宫内膜癌转移中的机制
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批准号:81060175
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项目类别:地区科学基金项目
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资助金额:30.0万元
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批准年份:2010
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负责人:李崎
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依托单位: