首页> 外文期刊>FEBS Letters >Monosialyl‐Gb5 organized with cSrc and FAK in GEM of human breast carcinoma MCF‐7 cells defines their invasive properties
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Monosialyl‐Gb5 organized with cSrc and FAK in GEM of human breast carcinoma MCF‐7 cells defines their invasive properties

机译:在人乳腺癌MCF-7细胞的GEM中由cSrc和FAK组成的Monosialyl-Gb5定义了其侵袭特性

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>Two human mammary carcinoma cell variants, MCF-7/AZ and MCF-7/6, show the same composition in their glycosphingolipid-enriched microdomain (GEM) with regard to globo-series structures Gb3, Gb4, Gb5, monosialyl-Gb5, GM2, and cSrc and FAK. Both variants are non-invasive into collagen gel layer, and showed similar motility in wound migration assay. Whereas invasiveness and motility of MCF-7/AZ cells were enhanced greatly by treatment with mAb RM1 directed to monosialyl-Gb5, the same RM1 treatment had no effect on MCF-7/6. cSrc and FAK of MCF-7/AZ, but not MCF-7/6, were activated by RM1 treatment. Thus, malignancy of MCF-7 is highly dependent on monosialyl-Gb5, and its activation of cSrc and FAK in GEM.
机译:>两个人类乳腺癌细胞变体MCF-7 / AZ和MCF-7 / 6在富含糖鞘脂的微域(GEM)中显示出与球序列系列Gb3,Gb4,Gb5,单唾液酸基- Gb5,GM2和cSrc和FAK。两种变体均无创性进入胶原凝胶层,并且在伤口迁移试验中显示出相似的运动性。尽管通过针对单唾液酸基-Gb5的mAb RM1处理可大大增强MCF-7 / AZ细胞的侵袭性和运动性,但相同的RM1处理对MCF-7 / 6无影响。 RM1处理激活了MCF-7 / AZ的cSrc和FAK,但未激活MCF-7 / 6。因此,MCF-7的恶性高度依赖于单唾液酸基-Gb5及其在GEM中对cSrc和FAK的激活。

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