Gene transfection in human keratinocyte and melanocyte
人角质形成细胞和黑素细胞的基因转染
基本信息
- 批准号:11671780
- 负责人:
- 金额:$ 2.24万
- 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:1999
- 资助国家:日本
- 起止时间:1999 至 2000
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
1 At first, we studied the transfection of ha-tagged human gelsolin cDNA in human squamous carcinomacell line HEC46 and human melanoma cell line in stead of keratinocyte and melanocyte. We used human melanoma tissue and normal skin tissue as a control, and found out a unique 85Kda protein in Western blotting.2 By Western blotting analysis of 38 melanoma samples for the expression of gelsolin using anti-gelsolin antibodies, we identified a new truncated variant of gelsolin p85 (GSNp85) lacking the C-terminal domain, which was always co-expressed with wild type gelsolin. The GSNp85 variant was more frequently expressed in vertical growth phase (VGP) melanomas as compared to radial growth phase (RGP) melanomas and was not expressed in other skin cancers, normal skin tissues, and nevi tissues except for 2 congenital junctional types. These data suggest that the occurrence of GSNp85 in melanoma may be a new indicator for the advanced stage of the tumor.
1起初,我们研究了在人类鳞状癌系HEC46和人类黑色素瘤细胞系中的转染中的HA标记的人凝胶蛋白cDNA,而不是角质类细胞和黑素细胞。 We used human melanoma tissue and normal skin tissue as a control, and found out a unique 85Kda protein in Western blotting.2 By Western blotting analysis of 38 melanoma samples for the expression of gelsolin using anti-gelsolin antibodies, we identified a new truncated variant of gelsolin p85 (GSNp85) lacking the C-terminal domain, which was always co-expressed with wild type凝胶林。与径向生长阶段(RGP)黑色素瘤相比,GSNP85变体在垂直生长阶段(VGP)黑色素瘤中更常见,并且在其他皮肤癌,正常的皮肤组织和NEVI组织中未表达,除2种先天性连接类型外。这些数据表明,黑色素瘤中GSNP85的发生可能是肿瘤晚期阶段的新指标。
项目成果
期刊论文数量(3)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
古川洋志: "悪性黒色腫におけるゲルソリン短縮体の発現と腫瘍浸潤度との関係"北海道医学雑誌. 76巻3号(掲載予定). (2001)
Hiroshi Furukawa:“恶性黑色素瘤中凝溶胶蛋白截短形式的表达与肿瘤侵袭性的关系”《北海道医学杂志》第 76 卷,第 3 期(待出版)。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Furukawa, H.: "Relationship between the Expression of a Gelsolin Truncate and Invasiveness in Malignant Melanoma."Hokkaido Journal of Medical Science. 76 (3)(in press). (2001)
Furukawa, H.:“凝溶胶蛋白截短物的表达与恶性黑色素瘤侵袭性之间的关系。”北海道医学科学杂志。
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- 影响因子:0
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YAMAMOTO Yuhei其他文献
YAMAMOTO Yuhei的其他文献
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{{ truncateString('YAMAMOTO Yuhei', 18)}}的其他基金
Identification of sources of anthropogenic aerosols using vanadium composition and lead isotope ratio origin from coal combustion
利用源自煤燃烧的钒成分和铅同位素比来识别人为气溶胶的来源
- 批准号:
20K05585 - 财政年份:2020
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Development of functional lymph node transfer
功能性淋巴结转移的发展
- 批准号:
16H05491 - 财政年份:2016
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Effect of immunosuppressive agents on the interaction between keloid fibroblasts and CD4+ T cells in a coculture model
共培养模型中免疫抑制剂对瘢痕疙瘩成纤维细胞与 CD4 T 细胞相互作用的影响
- 批准号:
25670745 - 财政年份:2013
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Challenging Exploratory Research
Does HGF act as a inhibitor of TGF-β mediated keloid formation?
HGF 是否可以作为 TGF-β 介导的瘢痕疙瘩形成的抑制剂?
- 批准号:
23659825 - 财政年份:2011
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Challenging Exploratory Research
Dynamic change of Myogenin in denervated rat mimetic muscle: Does the neural repair repress its expression ?
去神经大鼠模拟肌中肌生成素的动态变化:神经修复是否抑制其表达?
- 批准号:
22390331 - 财政年份:2010
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Development of novel therapy for malignant melanoma by morphogenetic gene transfer
通过形态发生基因转移开发恶性黑色素瘤新疗法
- 批准号:
18390476 - 财政年份:2006
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
A new treatment approach for Malignant Melanoma basing on analysis of expression pattern of homeobox genes
基于同源框基因表达模式分析的恶性黑色素瘤新治疗方法
- 批准号:
16390505 - 财政年份:2004
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Analysis of Master Genes Associated with Invasion and Metastasis by Malignant Melanoma
恶性黑色素瘤侵袭和转移相关主基因分析
- 批准号:
13470377 - 财政年份:2001
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
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