Ontology highlight
ABSTRACT: Background
Gastric cancer (GC) is among the most common and deadliest cancers globally. Many long non-coding RNAs (lncRNAs) are key regulators of GC pathogenesis. This study aimed to define the role of HOXA-AS3 in this oncogenic context.Methods
Levels of HOXA-AS3 expression in GC were quantified via qPCR. The effects of HOXA-AS3 knockdown on GC cells function were evaluated in vitro using colony formation assays, wound healing assays and transwell assays. Subcutaneous xenograft and tail vein injection tumor model systems were generated in nude mice to assess the effects of this lncRNA in vivo. The localization of HOXA-AS3 within cells was confirmed by subcellular fractionation, and predicted microRNA (miRNA) targets of this lncRNA and its ability to modulate downstream NF-?B signaling in GC cells were evaluated via luciferase-reporter assays, immunofluorescent staining, and western blotting.Results
GC cells and tissues exhibited significant HOXA-AS3 upregulation (P?ConclusionHOXA-AS3/miR-29a-3p/LT?R/NF-?B regulatory axis contributes to the progression of GC, thereby offering novel target for the prognosis and treatment of GC.
SUBMITTER: Qu F
PROVIDER: S-EPMC7890634 | biostudies-literature | 2021 Feb
REPOSITORIES: biostudies-literature
Qu Feng F Zhu Bin B Hu Yi-Lin YL Mao Qin-Sheng QS Feng Ying Y
Cancer cell international 20210218 1
<h4>Background</h4>Gastric cancer (GC) is among the most common and deadliest cancers globally. Many long non-coding RNAs (lncRNAs) are key regulators of GC pathogenesis. This study aimed to define the role of HOXA-AS3 in this oncogenic context.<h4>Methods</h4>Levels of HOXA-AS3 expression in GC were quantified via qPCR. The effects of HOXA-AS3 knockdown on GC cells function were evaluated in vitro using colony formation assays, wound healing assays and transwell assays. Subcutaneous xenograft a ...[more]