| Literature DB >> 24727449 |
Ki Hyung Kim1, Yun-Jeong Kang2, Jin-Ok Jo2, Mee Sun Ock2, Soo Hyun Moon1, Dong Soo Suh1, Man Soo Yoon1, Eun-Sil Park3, Namkung Jeong4, Wan-Kyu Eo5, Heung Yeol Kim6, Hee-Jae Cha7.
Abstract
DDX4 (DEAD box polypeptide 4), characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), is an RNA helicase which is implicated in various cellular processes involving the alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. DDX4 is known to be a germ cell-specific protein and is used as a sorting marker of germline stem cells for the production of oocytes. A recent report about DDX4 in ovarian cancer showed that DDX4 is overexpressed in epithelial ovarian cancer and disrupts a DNA damage-induced G2 checkpoint. We investigated the relationship between DDX4 and ovarian cancer stem cells by analyzing the expression patterns of DDX4 and the cancer stem cell marker CD133 in ovarian cancers via tissue microarray. Both DDX4 and CD133 were significantly increased in ovarian cancer compared to benign tumors, and showed similar patterns of expression. In addition, DDX4 and CD133 were mostly colocalized in various types of ovarian cancer tissues. Furthermore, almost all CD133 positive ovarian cancer cells also express DDX4 whereas CD133-negative cells did not possess DDX4, suggesting a strong possibility that DDX4 plays an important role in cancer stem cells, and/or can be used as an ovarian cancer stem cell marker.Entities:
Keywords: CD133; Cancer stem cells; DDX4; Ovarian cancer
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Year: 2014 PMID: 24727449 DOI: 10.1016/j.bbrc.2014.03.144
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575