LINC00339 promotes gastric cancer progression by elevating DCP1A expression via inhibiting miR‐377‐3p
Up to date, the mechanism of gastric cancer (GC) development is poorly understood. This study was to demonstrate the effects of LINC00339 on GC progression. Here, we found that LINC00339 was overexpressed expressed in GC tissues and predicted poor outcome. By CCK8, colony formation and Transwell ass...
Saved in:
Published in | Journal of cellular physiology Vol. 234; no. 12; pp. 23667 - 23674 |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
01.12.2019
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Up to date, the mechanism of gastric cancer (GC) development is poorly understood. This study was to demonstrate the effects of LINC00339 on GC progression. Here, we found that LINC00339 was overexpressed expressed in GC tissues and predicted poor outcome. By CCK8, colony formation and Transwell assays, we showed LINC00339 knockdown suppressed GC cell proliferation, migration, and invasion in vitro. Flow cytometry analysis (FACS) indicated that LINC00339 knockdown induced tumor cell apoptosis. Besides, we utilized the xenograft assay and found that LINC00339 depletion led to decreased tumor growth in vivo. Mechanistically, miR‐377‐3p was found to be inhibited by LINC00339. And LINC00339 suppressed miR‐377‐3p to upregulate DCP1A, which consequently promoted GC progression. In conclusion, LINC00339 promotes gastric cancer progression by elevating DCP1A expression via inhibiting miR‐377‐3p.
LINC00339 promotes gastric cancer progression by elevating DCP1A expression via inhibiting miR‐377‐3p. |
---|---|
Bibliography: | Chengmin Shi, Tonglei Liu, and Junlin Chi contributed equally to this study. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Correction/Retraction-3 |
ISSN: | 0021-9541 1097-4652 1097-4652 |
DOI: | 10.1002/jcp.28934 |