CXCL14/BRAK is a multifunctional tumor suppressor
CXCL14/BRAK is a multifunctional tumor suppressor
批准号:
22390353
负责人:
HATA Ryu-ichiro
金额:
$12.73万
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:
2010
资助国家:
日本
项目状态:
已结题
起止时间:
2010 至 2012
中文摘要
目的:研究趋化因子Brak/CXCL14转基因(TG)小鼠对肿瘤的发生、生长和转移是否具有抵抗力。方法:给野生型C57BL/6(Wt)或Tg小鼠腹腔注射12 mg/kg体重的偶氮甲烷,然后在饮用水中间歇加入3%葡聚糖硫酸钠。我们还将肿瘤细胞注射到小鼠的皮下或尾静脉。结果:Wt小鼠和Tg小鼠体重无明显差异,但Wt小鼠结直肠癌的发生率是Tg小鼠的近10倍(P<;0.001)。移植瘤大小和肺转移灶数目,试验组均明显低于对照组。注射黑色素瘤细胞的Tg小鼠存活率明显高于Wt小鼠。结论:BRAK/CXCL14对肿瘤的发生、生长和转移均有抵抗作用,提示Brak/CXCL14具有多种抑瘤作用。
英文摘要
Objectives: The aim of this study was to determine whether or not chemokine BRAK/ CXCL14 transgenic (Tg) mice would show resistance to carcinogenesis, tumor growth and tumor metastasis. Methods: Wild type C57BL/6 (Wt) or Tg mice were injected intraperitoneally with 12 mg/kg body weight azoxymethane followed by intermittent addition of 3 % dextran sodium sulfate in the drinking water. We also injected tumor cells subcutaneously or via a tail vein of the mice. Results: No difference of body weight was observed between Wt and Tg mice but the rate of colorectal cancer was nearly ten times higher (P<0.001) in Wt mice than in Tg ones. Size of transplanted tumors and the number of metastatic foci on the lung of the animals were always significantly lower in the Tg that those in the Wt. Survival rates of the melanoma cell injected Tg mice were significantly higher than those of Wt. Conclusion: The Tg mice showed resistance to carcinogenesis, tumor growth and tumor cell metastasis, indicating BRAK/ CXCL14 has multifunctional effects on tumor suppression.
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Oxidative stress reduces expression of CXCL14/BRAK in human SCC cells
氧化应激降低人鳞状细胞癌细胞中 CXCL14/BRAK 的表达
DOI:
--
发表时间:
2011
期刊:
影响因子:
--
作者:
[Maehata Y, Ozawa S, Miyamoto C, Kobayashi K, Komori R, Hata R, Lee M]
通讯作者:
Lee M
ROCK阻害剤(Fasudi1)は抗腫瘍性ケモカイン(CXCL14/BRAK)の細胞外分泌促進を介して腫瘍進展を抑制する
ROCK 抑制剂 (Fasudi1) 通过促进抗肿瘤趋化因子 (CXCL14/BRAK) 的细胞外分泌来抑制肿瘤进展
DOI:
--
发表时间:
2011
期刊:
影响因子:
--
作者:
[宮本千央, 前畑洋次郎, 小澤重幸, 生駒丈晴, 小森令賀, 居作和人, 加藤靖正, 畑隆一郎, 李昌一]
通讯作者:
李昌一
Fasudil, a specific inhibitor of ROCK, stimulates secretion of CXCL14/BRAK and suppresses tumor growth in vivo
Fasudil 是 ROCK 的特异性抑制剂,可刺激 CXCL14/BRAK 的分泌并抑制体内肿瘤生长
DOI:
--
发表时间:
2011
期刊:
影响因子:
--
作者:
[Miyamoto C., Maehata Y., Ozawa S., Ikoma T., Komori R., Hata R.-I., Lee M-C.]
通讯作者:
Lee M-C.
DOI:
10.1254/jphs.12177fp
发表时间:
2012-11-01
期刊:
JOURNAL OF PHARMACOLOGICAL SCIENCES
影响因子:
3.5
作者:
[Miyamoto, Chihiro, Maehata, Yojiro, Lee, Masaichi-Chang-il]
通讯作者:
Lee, Masaichi-Chang-il
NK cells are indispensable for suppression of tumor growth and metastasis in transgenic mice over-expressing chemokine CXCL14/BRAK
NK细胞对于抑制过度表达趋化因子CXCL14/BRAK的转基因小鼠的肿瘤生长和转移是不可或缺的
DOI:
--
发表时间:
2012
期刊:
影响因子:
--
作者:
[Hata R, Izukuri K, Kato Y, Takeda K, Kiyono T, Mukaida N, Taniguchi M]
通讯作者:
Taniguchi M
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Cell-matrix interactions in bone formation and regeneration
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批准号:14370598
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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:2002
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负责人:HATA Ryu-ichiro
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依托单位:
海外基金