The long non-coding RNA EPB41L4A-AS2 inhibits tumor proliferation and is associated with favorable prognoses in breast cancer and other solid tumors

2016 
// Shouping Xu 1 , Peiyuan Wang 1 , Zilong You 1 , Hongxue Meng 2 , Guannan Mu 3 , Xianan Bai 1 , Guangwen Zhang 1 , Jinfeng Zhang 1 , Da Pang 1, 4 1 Department of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, China 2 Department of Pathology, Harbin Medical University Cancer Hospital, Harbin, China 3 Biotherapy Center, Harbin Medical University Cancer Hospital, Harbin, China 4 Heilongjiang Academy of Medical Sciences, Harbin, China Correspondence to: Da Pang, e-mail: pangda@ems.hrbmu.edu.cn Keywords: antisense lncRNA, EPB41L4A-AS2, prognostic value, proliferation, breast cancer Received: November 12, 2015      Accepted: February 18, 2016      Published: March 09, 2016 ABSTRACT EPB41L4A-AS2 is a novel long non-coding RNA of unknown function. In this study, we investigated the expression of EPB41L4A-AS2 in breast cancer tissues and evaluated its relationship with the clinicopathological features and prognosis of patients with breast cancer. This entailed conducting a meta-analysis and prognosis validation study using two cohorts from the Gene Expression Omnibus (GEO). In addition, we assessed EPB41L4A-AS2 expression and its relationship with the clinicopathological features of renal and lung cancers using the Cancer Genome Atlas cohort and a GEO dataset. We also clarified the role of EPB41L4A-AS2 expression in mediating cancer cell proliferation in breast, renal, and lung cancer cell lines transfected with an EPB41L4A-AS2 expression vector. We found that high EPB41L4A-AS2 expression is associated with favorable disease outcomes. Gene ontology enrichment analysis revealed that EPB41L4A-AS2 may be involved in processes associated with tumor biology. Finally, overexpression of EPB41L4A-AS2 inhibited tumor cell proliferation in breast, renal, and lung cancer cell lines. Our clinical and in vitro results suggest that EPB41L4A-AS2 inhibits solid tumor formation and that evaluation of this long non-coding RNA may have prognostic value in the clinical management of such malignancies.
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