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1型B类清道夫受体调节神经母细胞瘤细胞的增殖、迁移和侵袭。

Scavenger receptor class B type 1 regulates neuroblastoma cell proliferation, migration and invasion.

作者信息

Panchoo Marlyn, Lacko Andras

机构信息

Department of Physiology and Anatomy, University of North Texas Health Science Center, 3500 Camp Bowie Boulevard, Fort Worth, Tx, 76107, USA.

出版信息

Biochem Biophys Res Commun. 2018 Jan 1;495(1):614-620. doi: 10.1016/j.bbrc.2017.10.154. Epub 2017 Nov 9.

Abstract

Neuroblastoma (NB) is an extra cranial pediatric embryonal tumor most prevalent in children less than 1 year of age. NB accounts for 7% of all pediatric cancers but accounts for 15% of all childhood cancer deaths. Scavenger receptor class B type 1 (SR-B1), a mediator of cellular cholesterol uptake, is overexpressed in and have been linked to the aggressiveness of many cancers. Nevertheless, no studies have so far investigated the relationship between SR-B1 and NB. Elucidation of receptors that promote NB may pave the way for discovery of new therapeutic targets. Here we show that inhibition of SR-B1 reduced cell survival, migration and invasion, and cholesterol content in NB cell lines. Additionally analysis of SR-B1 levels in NB patient biopsies using the R2: Genomics Analysis and Visualization Platform showed that high SR-B1 expression correlated with decreased overall and event-free survival.

摘要

神经母细胞瘤(NB)是一种颅外小儿胚胎性肿瘤,在1岁以下儿童中最为常见。NB占所有小儿癌症的7%,但占所有儿童癌症死亡人数的15%。清道夫受体B1类(SR-B1)是细胞胆固醇摄取的介质,在许多癌症中过度表达并与癌症的侵袭性有关。然而,迄今为止尚无研究调查SR-B1与NB之间的关系。阐明促进NB的受体可能为发现新的治疗靶点铺平道路。在此我们表明,抑制SR-B1可降低NB细胞系中的细胞存活、迁移和侵袭以及胆固醇含量。此外,使用R2:基因组分析和可视化平台对NB患者活检组织中的SR-B1水平进行分析表明,SR-B1高表达与总生存期和无事件生存期降低相关。

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