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抑癌基因 RKIP 抑制前列腺癌细胞转移,并增强前列腺癌细胞对多西紫杉醇治疗的敏感性。

Tumor suppressor RKIP inhibits prostate cancer cell metastasis and sensitizes prostate cancer cells to docetaxel treatment.

出版信息

Neoplasma. 2018;65(2):228-233. doi: 10.4149/neo_2018_170203N72.

Abstract

Raf kinase inhibitory protein (RKIP) is a well-established metastasis suppressor that is frequently down-regulated in aggressive cancers. However, the impact of RKIP on cancer cell invasion and metastasis in prostate cancer is still elusive. To this end, we overexpressed RKIP in two prostate cancer cell lines. We found that overexpression of RKIP inhibited prostate cancer cells proliferation, migration and invasion. Mechanistically, we found that RKIP overexpression led to down-regula- tion of the NF-kB signaling pathway and inhibition of the epithelial-to-mesenchymal transition, which is important step for cancer metastasis. In addition, overexpression of RKIP can promote drug effects of docetaxel on prostate cancer cell lines. In conclusion, overexpression of RKIP significantly inhibits prostate cancer cell migration and metastasis, and overexpression of RKIP could aid prostate cancer treatment and therapy.

摘要

Raf 激酶抑制蛋白(RKIP)是一种已被广泛证实的转移抑制因子,在侵袭性癌症中常被下调。然而,RKIP 对前列腺癌中癌细胞侵袭和转移的影响仍不清楚。为此,我们在两种前列腺癌细胞系中过表达了 RKIP。我们发现 RKIP 的过表达抑制了前列腺癌细胞的增殖、迁移和侵袭。从机制上讲,我们发现 RKIP 的过表达导致 NF-κB 信号通路的下调和上皮间质转化的抑制,这是癌症转移的重要步骤。此外,RKIP 的过表达可以促进多西紫杉醇对前列腺癌细胞系的药物作用。总之,RKIP 的过表达显著抑制了前列腺癌细胞的迁移和转移,RKIP 的过表达可能有助于前列腺癌的治疗和治疗。

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