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首页> 外文期刊>Biology of the cell >RNA interference of metastasis-associated gene 1 inhibits metastasis of B16F10 melanoma cells in a C57BL/6 mouse model.
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RNA interference of metastasis-associated gene 1 inhibits metastasis of B16F10 melanoma cells in a C57BL/6 mouse model.

机译:转移相关基因1的RNA干扰抑制了C57BL / 6小鼠模型中B16F10黑色素瘤细胞的转移。

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BACKGROUND INFORMATION: MTA1 (metastasis-associated gene 1) has been reported to be overexpressed in cancers with high potential to metastasize. Studies of the molecular mechanisms revealed that MTA1 plays an important role in the process of metastasis of many types of cancer. However, the role of MTA1 in melanoma development is unclear. RESULTS: We have investigated the therapeutic value of MTA1 in the B16F10 melanoma cell line with the C57BL/6 mouse model. Studies in vitro showed that MTA1 promoted the metastatic ability of B16F10 cancer cells. MTA1 down-regulation by RNA interference greatly reversed the malignant phenotypes of cancer cells. Immunohistochemical staining of MTA1 in human melanoma samples confirmed the up-regulation of MTA1 in the process of carcinogenesis. Studies in vivo confirmed down-regulation of MTA1 suppressed the growth and experimental metastasis of B16F10 melanoma cells. CONCLUSIONS: MTA1 plays an important role in melanoma development and metastasis. It has a promising potential as a target for in cancer gene therapy or chemotherapy.
机译:背景信息:据报道,MTA1(与转移有关的基因1)在具有高转移潜力的癌症中过表达。分子机制研究表明,MTA1在多种类型癌症的转移过程中起着重要作用。但是,MTA1在黑色素瘤发展中的作用尚不清楚。结果:我们研究了C57BL / 6小鼠模型在B16F10黑色素瘤细胞系中MTA1的治疗价值。体外研究表明,MTA1促进了B16F10癌细胞的转移能力。 RNA干扰使MTA1下调大大逆转了癌细胞的恶性表型。人类黑素瘤样品中MTA1的免疫组织化学染色证实了MTA1在癌变过程中的上调。体内研究证实,MTA1的下调抑制了B16F10黑色素瘤细胞的生长和实验转移。结论:MTA1在黑色素瘤的发展和转移中起着重要作用。作为癌症基因治疗或化学疗法的靶标,它具有广阔的前景。

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