Suppr超能文献

腺病毒介导的REIC/Dkk-3基因转移抑制原位前列腺癌模型中的肿瘤生长和转移。

Adenovirus-mediated REIC/Dkk-3 gene transfer inhibits tumor growth and metastasis in an orthotopic prostate cancer model.

作者信息

Edamura K, Nasu Y, Takaishi M, Kobayashi T, Abarzua F, Sakaguchi M, Kashiwakura Y, Ebara S, Saika T, Watanabe M, Huh N-H, Kumon H

机构信息

Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

出版信息

Cancer Gene Ther. 2007 Sep;14(9):765-72. doi: 10.1038/sj.cgt.7701071. Epub 2007 Jun 29.

Abstract

We had previously reported that REIC/Dkk-3, a member of the Dickkopf (Dkk) gene family, works as a tumor suppressor. In this study, we evaluated the therapeutic effects of an intratumoral injection with adenoviral vector encoding REIC/Dkk-3 gene (Ad-REIC) using an orthotopic mouse prostate cancer model of RM-9 cells. We also investigated the in vivo anti-metastatic effect and in vitro anti-invasion effect of Ad-REIC gene delivery. We demonstrated that the Ad-REIC treatment inhibited prostate cancer growth and lymph node metastasis, and prolonged mice survival in the model. These therapeutic responses were consistent with the intratumoral apoptosis induction and in vitro suppression of cell invasion/migration with reduced matrix metalloprotease-2 activity. We thus concluded that in situ Ad-REIC/Dkk-3 gene transfer may be a promising therapeutic intervention modality for the treatment of prostate cancer.

摘要

我们之前曾报道,Dickkopf(Dkk)基因家族成员REIC/Dkk-3作为一种肿瘤抑制因子发挥作用。在本研究中,我们使用RM-9细胞的原位小鼠前列腺癌模型,评估了瘤内注射编码REIC/Dkk-3基因的腺病毒载体(Ad-REIC)的治疗效果。我们还研究了Ad-REIC基因递送的体内抗转移作用和体外抗侵袭作用。我们证明,Ad-REIC治疗可抑制前列腺癌生长和淋巴结转移,并延长模型小鼠的生存期。这些治疗反应与瘤内凋亡诱导以及体外细胞侵袭/迁移抑制和基质金属蛋白酶-2活性降低相一致。因此,我们得出结论,原位Ad-REIC/Dkk-3基因转移可能是一种有前景的前列腺癌治疗干预方式。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验