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Mirtronic miR-4646-5p promotes gastric cancer metastasis by regulating ABHD16A and metabolite lysophosphatidylserines.

Authors :
Yang L
Hou Y
Du YE
Li Q
Zhou F
Li Y
Zeng H
Jin T
Wan X
Guan S
Wang R
Liu M
Source :
Cell death and differentiation [Cell Death Differ] 2021 Sep; Vol. 28 (9), pp. 2708-2727. Date of Electronic Publication: 2021 Apr 19.
Publication Year :
2021

Abstract

The aberrant classical miRNAs are considered to play significant roles in tumor progression. However, it remains unclear for nonclassical miRNAs, a set of Drosha-independent miRNAs in the process of various biology. Here, we reveal that a nonclassical miR-4646-5p plays a pivotal role in gastric cancer (GC) metastasis. MiR-4646-5p, one of Drosha-independent mirtronic miRNA, is aberrant up-regulated in Drosha-low expressed GC and Drosha-knockdown gastric cancer cells. Mirtronic miR-4646-5p is a specific transcription splicing product of intron 3 of the host gene Abhd16a with the aid of SRSF2. The enhanced miR-4646-5p can stabilize HIF1A by targeting PHD3 to positive feedback regulate Abhd16a and miR-4646-5p itself expressions. ABHD16A, as an emerging phosphatidylserine-specific lipase, involves in lipid metabolism leading to lysophosphatidylserines (lyso-PSs) accumulation, which stimulates RhoA and downstream LIMK/cofilin cascade activity through GPR34/Gi subunit, thus causes metastasis of gastric cancer. In addition, miR-4646-5p/PHD3/HIF1A signaling can also up-regulate RhoA expression and synergistically promote gastric cancer cell invasion and metastasis. Our study provides new insights of nonclassical mirtronic miRNA on tumor progress and may serve as a new diagnostic biomarker for gastric cancer. MiR-4646-5p and its host gene Abhd16a mediated abnormal lipid metabolism may be a new target for clinical treatment of gastric cancer.<br /> (© 2021. The Author(s).)

Details

Language :
English
ISSN :
1476-5403
Volume :
28
Issue :
9
Database :
MEDLINE
Journal :
Cell death and differentiation
Publication Type :
Academic Journal
Accession number :
33875796
Full Text :
https://doi.org/10.1038/s41418-021-00779-y