基因沉默
ROR1型
细胞凋亡
癌症研究
生物
细胞生物学
基因
遗传学
受体
血小板源性生长因子受体
生长因子
作者
Aniruddha Choudhury,Katja Derkow,Amir Hossein Daneshmanesh,Eva Mikaelsson,Shahryar Kiaii,Parviz Kokhaei,Anders Österborg,Håkan Mellstedt
标识
DOI:10.1111/j.1365-2141.2010.08362.x
摘要
Summary We have previously demonstrated that ROR1 and FMOD (fibromodulin) are two genes upregulated in chronic lymphocytic leukaemia (CLL) cells compared to normal blood B cells. In this study, siRNAs were used to specifically silence ROR1 and FMOD expression in CLL cells, healthy B cells and human fibroblast cell lines. siRNA treatment induced a specific reduction (75–95%) in FMOD and ROR1 mRNA. Western blot analysis with specific antibodies for FMOD and ROR1 demonstrated that the proteins were significantly downregulated 48 h after siRNA treatment. Silencing of FMOD and ROR1 resulted in statistically significant ( P ≤ 0·05–0·001) apoptosis of CLL cells but not of B cells from normal donors. Human fibroblast cell lines treated with FMOD and ROR1 siRNA did not undergo apoptosis. This is the first report demonstrating that ROR1 and FMOD may be involved in the survival of CLL cells. ROR1 in particular is further explored as potential target for therapy in CLL.
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