Long non-coding RNAs show different expression profiles and display competing endogenous RNA potential in placenta accreta spectrum disorders.
10.12122/j.issn.1673-4254.2019.10.19
- Author:
Shuzhen WU
1
;
Huishan ZHANG
1
;
Yan LIU
1
;
Rui WANG
1
;
Shaoxin YE
1
;
Meng ZENG
1
;
Zhengping LIU
1
Author Information
1. Department of Obstetrics, Foshan Maternal and Child Health Hospital Affiliated to Southern Medical University, Foshan 528000, China.
- Publication Type:Journal Article
- Keywords:
competing endogenous RNA network;
expression profile;
long non-coding RNAs;
placenta accreta spectrum
- From:
Journal of Southern Medical University
2019;39(10):1253-1259
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the expression profile of long non-coding RNAs (lncRNA) and identify potential lncRNA-related competing endogenous RNAs (ceRNA) in placenta accrete spectrum disorders (PAS).
METHODS:Five tissue specimens of placental implantation and 5 adjacent normal placental tissues were collected from cesarean section deliveries complicated by PAS in our hospital between December, 2017 and June, 2018. Human microarrays were used to identify the lncRNAs that were differentially expressed in PAS, and 5 of the identified lncRNAs were further validated using qRT-PCR. GO and KEGG pathway analyses were performed to indentify the most significant enrichment functions. A ceRNA network was constructed based on ENST00000511361 (RP5-875H18.4), NR_027457 (LINC00221) and NR_126415 (FOXP4-AS1) to pinpoint the potential lncRNAs-related ceRNA.
RESULTS:A total of 329 lncRNAs and 179 mRNAs were identified to have differential expression in PAS. The results of qRT-PCR were consistent with the human microarrays results. Transforming growth factor-β (TGF-β) signaling pathway was the most significantly enriched pathway. The constructed ceRNA network suggested that RP5-875H18.4--miRNA-218--SLIT2 had a potential ceRNA regulatory mechanism in PAS.
CONCLUSIONS:The differentially expressed lncRNAs are involved in the occurrence and progression of PAS possibly by regulating the TGF-β signaling pathway. The ceRNA network of RP5-875H18.4--miRNA-218--SLIT2 may play a role in the occurrence of PAS.
