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Establishment of Stable Focal adhesion kinase(FAK) RNA Interference Cell Line

机译:建立稳定焦粘连激酶(FAK)RNA干扰细胞系

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Malignant melanoma continues to remain a significant health threat, with death often occurring as a result of metastasis. Focal adhesion kinase (FAK) is a non-receptor protein tyrosine kinase implicated in cell cycle progression and cell migration. Overexpression of FAK in a variety of tumors has suggested that FAK is a promising target for therapeutic intervention. In our previous study, we have demonstrated that plasmid-encoded FAK small interfering RNA (siRNA) dramatically inhibited in vitro mouse melanoma cell line B16F10 proliferation and invasion. Here, to further investigated the functional role of FAK, we repressed FAK expression by stable transfection of plasmid-encoded FAK small interfering RNA (siRNA). This stable cell line will be used to investigate the molecular mechanisms that promote an aggressive phenotype of melanoma.
机译:恶性黑素瘤继续仍然是一个重要的健康威胁,死亡经常由于转移而发生。局灶性粘附激酶(FAK)是涉及细胞周期进展和细胞迁移的非受体蛋白酪氨酸激酶。在各种肿瘤中的FAK过度表达表明FAK是治疗干预的有希望的目标。在我们以前的研究中,我们已经证明了质粒编码的FAK小干扰RNA(siRNA)显着抑制体外小鼠黑色素瘤细胞系B16F10增殖和侵袭。在这里,为了进一步研究FAK的功能作用,通过稳定转染质粒编码的FAK小干扰RNA(siRNA)来抑制FAK表达。该稳定的细胞系将用于研究促进黑素瘤的侵袭性表型的分子机制。

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