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DDX53通过与SOX-2结合来调控癌症干细胞样特性。

DDX53 Regulates Cancer Stem Cell-Like Properties by Binding to SOX-2.

作者信息

Kim Youngmi, Yeon Minjeong, Jeoung Dooil

机构信息

Department of Biochemistry, Kangwon National University, Chunchon 24341, Korea.

出版信息

Mol Cells. 2017 May 31;40(5):322-330. doi: 10.14348/molcells.2017.0001. Epub 2017 May 2.

Abstract

This study investigated the role of cancer/testis antigen DDX53 in regulating cancer stem cell-like properties. DDX53 shows co-expression with CD133, a marker for cancer stem cells. DDX53 directly regulates the SOX-2 expression in anticancer drug-resistant Malme3M cells. DDX53 and miR-200b were found to be involved in the regulation of tumor spheroid forming potential of Malme3M and Malme3M cells. Furthermore, the self-renewal activity and the tumorigenic potential of Malme3M-CD133 (+) cells were also regulated by DDX53. A miR-200b inhibitor induced the direct regulation of SOX-2 by DDX53 We therefore, conclude that DDX53 may serve as an immunotherapeutic target for regulating cancer stem-like properties of melanomas.

摘要

本研究调查了癌胚抗原DDX53在调节癌症干细胞样特性中的作用。DDX53与癌症干细胞标志物CD133共表达。DDX53直接调节抗癌药物耐药的Malme3M细胞中SOX-2的表达。发现DDX53和miR-200b参与调节Malme3M和Malme3M细胞形成肿瘤球的潜能。此外,Malme3M-CD133(+)细胞的自我更新活性和致瘤潜能也受DDX53调节。miR-200b抑制剂诱导DDX53对SOX-2的直接调节。因此,我们得出结论,DDX53可能作为一种免疫治疗靶点,用于调节黑色素瘤的癌症干细胞样特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0f2/5463040/fd9e3a56309c/molce-40-5-322f1.jpg

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