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首页> 外文期刊>Tumour biology : >Intrahepatic metastasis by orthotopic implantation of a fragment of murine hepatoma and its related molecules.
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Intrahepatic metastasis by orthotopic implantation of a fragment of murine hepatoma and its related molecules.

机译:通过原位植入鼠肝癌及其相关分子的片段进行肝内转移。

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Intrahepatic metastasis is a major modality in the recurrence of hepatoma. Establishment of the intrahepatic metastasis model would be useful for evaluating new anticancer therapies and analyzing the molecular mechanisms of tumor metastasis. Orthotopic implantation of a fragment of CBO140C12 hepatoma into the liver resulted in the formation of a solitary tumor nodule and its intrahepatic metastasis. In contrast, implantation of ADras3 cancer cells did not show any metastasis on day 21. CBO140C12 cells showed enhancement of the invasive, adhesive and migratory capabilities, as compared with ADras3 cells. Furthermore, mRNA expression and gelatinolytic activity of MMP-9 were detected in CBO140C12 cells, and the expression of mRNA for MT1-MMP in CBO140C12 cells was greater than that in ADras3 cells. Thus, intrahepatic metastasis of CBO140C12 tumor might be involved in the enhancement of the invasiveness of tumor cells via marked expression of MMP-9 and MT1-MMP.
机译:肝内转移是肝癌复发的主要方式。肝内转移模型的建立将有助于评估新的抗癌治疗方法和分析肿瘤转移的分子机制。将CBO140C12肝癌片段原位植入肝脏会导致孤立性肿瘤结节的形成及其肝内转移。相反,植入ADras3癌细胞在第21天没有显示任何转移。与ADras3细胞相比,CBO140C12细胞显示出增强的侵袭,粘附和迁移能力。此外,在CBO140C12细胞中检测到MMP-9的mRNA表达和明胶分解活性,并且CBO140C12细胞中MT1-MMP的mRNA表达高于ADras3细胞。因此,CBO140C12肿瘤的肝内转移可能通过MMP-9和MT1-MMP的明显表达来参与肿瘤细胞的侵袭性增强。

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