LINC00857 knockdown inhibits cell proliferation and induces apoptosis via involving STAT3 and MET oncogenic proteins in esophageal adenocarcinoma.

Abstract:

:Esophageal adenocarcinoma (EAC) is one of the leading causes of cancer-related death worldwide, and the molecular biology of this cancer remains poorly understood. Recent evidence indicates that long non-coding RNAs are dysregulated in a variety of cancers including EAC. In this study, siRNA mediated gene knockdown, Western blot, RT-PCR, as well as oncogenic function assay were performed. We found that the cell proliferation, colony formation, invasion and migration were decreased after LINC00857 knockdown in EAC cell lines. We also found that knockdown LINC00857 could induce apoptosis. Mechanistically, we found that the MET, STAT3, c-Myc and p-CREB proteins were decreased after LINC00857 knockdown. Our study suggests that LINC00857 may play an important oncogenic role in EAC via STAT3 and MET signaling.

journal_name

Aging (Albany NY)

journal_title

Aging

authors

Su W,Wang L,Niu F,Zou L,Guo C,Wang Z,Yang X,Wu J,Lu Y,Zhang J,Beer DG,Yang Z,Chen G

doi

10.18632/aging.101953

subject

Has Abstract

pub_date

2019-05-13 00:00:00

pages

2812-2821

issue

9

issn

1945-4589

pii

101953

journal_volume

11

pub_type

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