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Inhibition of DLX4 promotes apoptosis in choriocarcinoma cell lines.

作者信息

Sun Y, Lu X, Yin L, Zhao F, Feng Y

机构信息

Hospital of Obstetrics & Gynecology, Fudan University, 419 Fangxie Road, Shanghai 200011, China.

出版信息

Placenta. 2006 Apr-May;27(4-5):375-83. doi: 10.1016/j.placenta.2005.03.007. Epub 2005 Jun 21.

Abstract

Homeodomain (HDM) proteins encoded by homeobox (HBX) genes represent a large family of transcriptional factors that control differentiation and development in certain cell types. DLX4 is a member of Distal-less (DLX) family of HBX genes. Recent studies have demonstrated that abnormal expression of DLX4 is present in several types of human tumors, such as breast cancer, leukemia and colon cancer. In the present study, we investigated DLX4 mRNA and protein expression in both normal placental tissues and human choriocarcinoma cell lines. Also, using RNA interference (RNAi) technique, we knocked down the expression of DLX4 and examined apoptosis in JEG-3 cells. Our studies demonstrated that DLX4 RNAi inhibited DLX4 mRNA expression and decreased DLX4 protein mass specifically and effectively, potentially enhancing apoptosis. Moreover, we examined expression of caspase-3 and caspase-8, and found that both caspases were increased after DLX4 knockdown. However, DLX4 RNAi did not influence Bax expression in JEG-3 cells. In conclusion, this study suggests that DLX4 may be involved in the survival of human choriocarcinoma cells, which may be mediated by the inhibition of apoptosis. The detailed mechanism needs further investigation.

摘要

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