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长链非编码RNA HOTTIP可增强胰腺癌细胞的增殖、存活及迁移能力。

The long non-coding RNA HOTTIP enhances pancreatic cancer cell proliferation, survival and migration.

作者信息

Cheng Yating, Jutooru Indira, Chadalapaka Gayathri, Corton J Christopher, Safe Stephen

机构信息

Department of Veterinary Physiology and Pharmacology, Texas A&M University, College Station, TX 77843, USA.

Covance, Inc., Madison, WI 53704, USA.

出版信息

Oncotarget. 2015 May 10;6(13):10840-52. doi: 10.18632/oncotarget.3450.

Abstract

HOTTIP is a long non-coding RNA (lncRNA) transcribed from the 5' tip of the HOXA locus and is associated with the polycomb repressor complex 2 (PRC2) and WD repeat containing protein 5 (WDR5)/mixed lineage leukemia 1 (MLL1) chromatin modifying complexes. HOTTIP is expressed in pancreatic cancer cell lines and knockdown of HOTTIP by RNA interference (siHOTTIP) in Panc1 pancreatic cancer cells decreased proliferation, induced apoptosis and decreased migration. In Panc1 cells transfected with siHOTTIP, there was a decrease in expression of 757 genes and increased expression of 514 genes, and a limited gene analysis indicated that HOTTIP regulation of genes is complex. For example, Aurora kinase A, an important regulator of cell growth, is coregulated by MLL and not WDR5 and, in contrast to previous studies in liver cancer cells, HOTTIP does not regulate HOXA13 but plays a role in regulation of several other HOX genes including HOXA10, HOXB2, HOXA11, HOXA9 and HOXA1. Although HOTTIP and the HOX-associated lncRNA HOTAIR have similar pro-oncogenic functions, they regulate strikingly different sets of genes in Panc1 cells and in pancreatic tumors.

摘要

HOTTIP是一种长链非编码RNA(lncRNA),由HOXA基因座的5'端转录而来,与多梳抑制复合物2(PRC2)以及含WD重复序列蛋白5(WDR5)/混合谱系白血病1(MLL1)染色质修饰复合物相关。HOTTIP在胰腺癌细胞系中表达,在Panc1胰腺癌细胞中通过RNA干扰(siHOTTIP)敲低HOTTIP可降低细胞增殖、诱导细胞凋亡并减少细胞迁移。在用siHOTTIP转染的Panc1细胞中,有757个基因的表达下降,514个基因的表达增加,有限的基因分析表明HOTTIP对基因的调控很复杂。例如,细胞生长的重要调节因子极光激酶A由MLL共同调节而非WDR5,与先前在肝癌细胞中的研究不同,HOTTIP不调节HOXA13,但在包括HOXA10、HOXB2、HOXA11、HOXA9和HOXA1在内的其他几个HOX基因的调控中发挥作用。尽管HOTTIP和与HOX相关的lncRNA HOTAIR具有相似的促癌功能,但它们在Panc1细胞和胰腺肿瘤中调控截然不同的基因集。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09d4/4484423/be08330d3502/oncotarget-06-10840-g006.jpg

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