Evidence map›Paper›PMID 27270320›Full record

ArticleOncotarget2016

PIK3C2A mRNA functions as a miR-124 sponge to facilitate CD151 expression and enhance malignancy of hepatocellular carcinoma cells.

Tao Liu, Cai-Hua Zu, Shu-Sen Wang, Hong-Li Song, Zheng-Lu Wang, Xin-Nv Xu, Hong-Sheng Liu, Yu-Liang Wang, Zhong-Yang Shen

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 20 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Tao LiuKey Laboratory for Critical Care Medicine of The Ministry of Health, Tianjin First Central Hospital, Tianjin, China.
Cai-Hua ZuFirst Center Clinical College, Tianjin Medical University, Tianjin, China.
Shu-Sen WangKey Laboratory for Critical Care Medicine of The Ministry of Health, Tianjin First Central Hospital, Tianjin, China.
Hong-Li SongOrgan Transplant Center, Tianjin First Central Hospital, Tianjin, China.
Zheng-Lu WangDepartment of Pathology, Tianjin First Central Hospital, Tianjin, China.
Xin-Nv XuKey Laboratory for Critical Care Medicine of The Ministry of Health, Tianjin First Central Hospital, Tianjin, China.
Hong-Sheng LiuKey Laboratory for Critical Care Medicine of The Ministry of Health, Tianjin First Central Hospital, Tianjin, China.
Yu-Liang WangKey Laboratory for Critical Care Medicine of The Ministry of Health, Tianjin First Central Hospital, Tianjin, China.
Zhong-Yang ShenKey Laboratory for Critical Care Medicine of The Ministry of Health, Tianjin First Central Hospital, Tianjin, China.
Tianjin Medical University · CNTianjin First Center Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Competing endogenous RNAs (ceRNAs) are RNA transcripts that can crosstalk with each other by competing for shared microRNAs (miRNAs) through miRNA response elements (MREs). Involved in ceRNA networks, the RNA transcripts may be in a balance, disruption of which could lead to tumorigenesis. Here we reveal a ceRNA interaction between PIK3C2A and CD151 mRNAs in hepatocellular carcinoma (HCC) cells. PIK3C2A is a candidate ceRNA of CD151 because mRNA 3' untranslated regions (3'UTRs) of these two genes contain miR-124 binding sites. miR-124 is downregulated, while PIK3C2A and CD151 are upregulated in HCC cells compared with normal hepatocytes. Direct and negative regulation of PIK3C2A and CD151 by miR-124 was confirmed in HCC cells. miR-124 and the two potential ceRNAs are all recruited to the RNA-induced silencing complex (RISC). In HCC cell lines QGY- 7703 and SMMC-7721, and normal hepatic cell line HL-7702, miR-124 plays a tumor suppressor role by targeting PIK3C2A and CD151. The MREs within PIK3C2A 3'UTR can independently stimulate CD151 expression level by acting as miR-124 decoys. PIK3C2A MREs enhance HCC cell malignancy by absorbing endogenous miR-124 and activating CD151 in HCC cells. We conclude that PIK3C2A 3'UTR functions as a trans activator to stimulate CD151 by competing for miR-124 binding in HCC cells. The collaboration of PIK3C2A and CD151 through ceRNA mechanism may be implicated in HCC initiation and development.

Indexed as

Gene Expression Regulation, Neoplastic3' Untranslated RegionsAnimalsBinding SitesCarcinogenesisCarcinoma, HepatocellularCell Line, TumorGenes, Tumor SuppressorHepatocytesHumansLiver NeoplasmsMaleMice, Inbred BALB CMice, NudeMicroRNAsPhosphatidylinositol 3-Kinases3' Untranslated RegionsCD151 protein, humanMicroRNAsMIRN124 microRNA, humanPhosphatidylinositol 3-KinasesPIK3C2A protein, humanRNA-Induced Silencing ComplexTetraspanin 24CD151competing endogenous RNAhepatocellular carcinomamicroRNAPIK3C2A

Identifiers

PMID27270320
PMCPMC5190030
OpenAlexW2414228737

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.