首页> 外文期刊>Reproductive sciences >Human nonmetastatic clone 23 type 1 gene suppresses migration of cervical cancer cells and enhances the migration inhibition of fungal immunomodulatory protein from Ganoderma tsugae.
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Human nonmetastatic clone 23 type 1 gene suppresses migration of cervical cancer cells and enhances the migration inhibition of fungal immunomodulatory protein from Ganoderma tsugae.

机译:人类非转移性克隆23 1型基因可抑制子宫颈癌细胞的迁移,并增强来自灵芝的真菌免疫调节蛋白的迁移抑制。

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摘要

The authors investigate the effects of human nonmetastatic clone 23 type 1 (nm23-H1 ) gene and fungal immunomodulatory protein-Ganoderma tsugae (FIP-gts) on the metastatic potential of cervical cancer cells and assess whether nm23-H1 can influence the action of FIP-gts using cell migration and invasion assays and gelatin zymography. The nm23-H1 gene was stably transfected into Caski cells, which lacked nm23-H1 expression. The results show that nm23-H1 stably transfected Caski cells exhibit reduced cell migration but no change of cell invasion and matrix metalloproteinase (MMP)-2 and -9 activities. FIP-gts reduced cell migration in SiHa and nm23-H1 transfected Caski cells more significantly compared with Caski cells and reduced invasion in Caski and nm23-H1-transfected Caski cells, but it exerted no influence on MMP-2 and MMP-9 activities in them. Conclusively, the nm23-H1 gene suppresses cervical cancer cell migration but not invasion and activities of MMP-2 and MMP-9 and enhances the inhibition of FIP-gts upon migration.
机译:作者研究了人类非转移性克隆23型1(nm23-H1)基因和真菌免疫调节蛋白-灵芝(FIP-gts)对宫颈癌细胞转移潜能的影响,并评估nm23-H1是否可以影响FIP的作用-gts使用细胞迁移和侵袭试验以及明胶酶谱分析。将nm23-H1基因稳定转染到缺少nm23-H1表达的Caski细胞中。结果表明,nm23-H1稳定转染的Caski细胞显示出减少的细胞迁移,但细胞侵袭和基质金属蛋白酶(MMP)-2和-9活性没有变化。与Caski细胞相比,FIP-gts减少了SiHa和nm23-H1转染的Caski细胞中的细胞迁移,并减少了Caski和nm23-H1转染的Caski细胞中的侵袭,但对MMP-2和MMP-9活性没有影响。他们。结论是,nm23-H1基因抑制子宫颈癌细胞迁移,但不抑制MMP-2和MMP-9的侵袭和活性,并增强迁移时对FIP-gts的抑制作用。

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