生物
E2F型
癌基因
癌变
放大器
细胞周期
分子生物学
癌症研究
基因
细胞生长
遗传学
聚合酶链反应
作者
Husam Darwish,J M Cho,Martin Loignon,Moulay A. Alaoui‐Jamali
出处
期刊:Oncogene
[Springer Nature]
日期:2007-01-29
卷期号:26 (29): 4319-4328
被引量:35
标识
DOI:10.1038/sj.onc.1210195
摘要
The amplified region of chromosome 19q13.1–13.2 has been associated with several cancers. The well-characterized oncogene AKT2 is located in this amplicon. Two members of the same gene family (SERTAD1 and SERTAD3) are also located within this region. We report herein the genomic structure and potential functions of SERTAD3. SERTAD3 has two transcript variants with short mRNA half-lives, and one of the variants is tightly regulated throughout G1 and S phases of the cell cycle. Overexpression of SERTAD3 induces cell transformation in vitro and tumor formation in mice, whereas inhibition of SERTAD3 by small interfering RNA (siRNA) results in a reduction in cell growth rate. Furthermore, luciferase assays based on E2F-1 binding indicate that SERTAD3 increases the activity of E2F, which is reduced by inhibition of SERTAD3 by siRNA. Together, our data support that SERTAD3 contributes to oncogenesis, at least in part, via an E2F-dependent mechanism.
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