Evidence map›Paper›PMID 32654025›Full record

ArticlePathology oncology research : POR2020

Overexpression of Long Non-Coding RNA FGF14-AS2 Inhibits Colorectal Cancer Proliferation Via the RERG/Ras/ERK Signaling by Sponging microRNA-1288-3p.

Ruizhi Hou, Yan Liu, Yanzhuo Su, Zhenbo Shu

Abstract read
PubMed Publisher
In one paragraph

Article in Pathology oncology research : POR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
  2. Tumor-Associated Macrophage Exosomal miR-142-5p Drives Prostate Cancer Neuroendocrine Differentiation via RERG/Ras/ERK Axis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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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

4 authors at 3 institutions in 1 country.

Ruizhi HouDepartment of Gastrointestinal Colorectal Surgery, the Third Hospital of Jilin University, Jilin University, Changchun, Jilin, 130033, China.
Yan LiuDepartment of Ultrasound, the Third Hospital of Jilin University, Jilin University, Changchun, Jilin, 130033, China.
Yanzhuo SuDepartment of Gastrointestinal Colorectal Surgery, the Third Hospital of Jilin University, Jilin University, Changchun, Jilin, 130033, China.
Zhenbo ShuDepartment of Gastrointestinal Colorectal Surgery, the Third Hospital of Jilin University, Jilin University, Changchun, Jilin, 130033, China. shuzhenbobo@outlook.com.
First Hospital of Jilin University · CNJilin Medical University · CNJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer remains one of most common cancer types with poor prognosis globally. Recent years, numerous studies depicted pivotal roles of lncRNAs in colorectal cancer progression. This study aimed to investigate the role of FGF14-AS2 in colorectal cancer development. FGF14-AS2 was found as a significantly downregulated lncRNA in TCGA dataset. Via RT-qPCR, we confirmed the downregulation of FGF14-AS2 in collected colorectal carcinoma samples. Transfection of plasmid containing full length of FGF14-AS2 repressed cell proliferation and induced elevation of cell apoptosis in colorectal cancer cells. In addition, FGF14-AS2 overexpression inactivated MAPK/ERK signaling in cells. Bioinformatic analysis and subsequent cell-based assays showed that FGF14-AS2 sponging miR-1288-3p, an oncogenic miRNA in colorectal cancer. RERG, the regulator of Ras/ERK pathway, was predicted and verified as target gene of miR-1288. Via downregulation of miR-1288, FGF14-AS2 elevated RERG expression in colorectal cancer cells. Rescue assays indicated that FGF14-AS2 relied on regulation of RERG to control cell proliferation and apoptosis in colorectal cancer. Taken together, the current study demonstrated FGF14-AS2 as a regulator of colorectal cancer development via downregulation of miR-1288-3p and inactivation of Ras/ERK signaling.

Indexed as

Gene Expression Regulation, NeoplasticApoptosisBiomarkers, TumorCell MovementCell ProliferationColorectal NeoplasmsFibroblast Growth FactorsGTP PhosphohydrolasesHumansMAP Kinase Signaling SystemMicroRNAsPrognosisras ProteinsRNA, AntisenseRNA, Long NoncodingTumor Cells, CulturedBiomarkers, Tumorfibroblast growth factor 14Fibroblast Growth FactorsGTP PhosphohydrolasesMicroRNAsMIRN1288 microRNA, humanras ProteinsRERG protein, humanRNA, AntisenseRNA, Long NoncodingColorectal cancerFGF14-AS2RERG

Identifiers

PMID32654025
OpenAlexW3042150802

What OpenQuestion holds

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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.