Evidence map›Paper›PMID 39951875›Full record

ArticleClinics (Sao Paulo, Brazil)2025

Circular RNA pappalysin-1 enhances glycolysis via microRNA-656-3p targeting G-protein subunit gamma-5 to promote colon cancer progression.

AiYuan Cai, HuiShi Ye, YuanHong Lin, JinYun Li, DongSheng Fang, ZhongBin Pan, ZhiWei Li, GuangLiang Luo, YanFang Huang, CiAi Lai

Abstract read
In one paragraph

Article in Clinics (Sao Paulo, Brazil), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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

10 authors.

AiYuan CaiDepartment of Paediatrics, Shenzhen Hospital (Futian) of Guangzhou University of Chinese Medicine, Shenzhen City 518034, Guangdong Province, PR China.
HuiShi YeDepartment of Paediatrics, Dongguan Hospital of Guangzhou University of Chinese Medicine, Dongguan City, Guangdong Province, PR China.
YuanHong LinSecond Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou City, Guangdong Province, PR China.
JinYun LiAcupuncture Rehabilitation Clinical College, Guangzhou University of Chinese Medicine, Guangzhou City, Guangdong Province, PR China.
DongSheng FangAcupuncture Rehabilitation Clinical College, Guangzhou University of Chinese Medicine, Guangzhou City, Guangdong Province, PR China.
ZhongBin PanSecond Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou City, Guangdong Province, PR China.
ZhiWei LiXi 'an Jiaotong University, Xi 'an City, Shaanxi Province, PR China.
GuangLiang LuoDepartment of Paediatrics, Shenzhen Hospital (Futian) of Guangzhou University of Chinese Medicine, Shenzhen City 518034, Guangdong Province, PR China.
YanFang HuangDepartment of Paediatrics, Shenzhen Hospital (Futian) of Guangzhou University of Chinese Medicine, Shenzhen City 518034, Guangdong Province, PR China.
CiAi LaiDepartment of Paediatrics, Shenzhen Hospital (Futian) of Guangzhou University of Chinese Medicine, Shenzhen City 518034, Guangdong Province, PR China. Electronic address: zhaohuiyin163@outlook.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveColon Cancer (CC) is a common malignant tumor. The aim of this study was to investigate the role and regulatory mechanism of circular RNA pappalysin-1 (circ-PAPPA; hsa_circ_0088233) in CC.

methodsIn cancer tissues from CC patients, circ-PAPPA expression was measured and its relationship with patients' clinical features was analyzed. Plasmid vectors or oligonucleotides interfering with the expression of circ-PAPPA, microRNA (miR)-656-3p or G-protein subunit Gamma-5 (GNG5) were transfected into CC cells. Cell viability was detected by MTT and colony formation assay; apoptosis was detected by flow cytometry; and cell migration and invasion were detected by wound healing assay and Transwell. Glycolytic capacity of CC cells was assessed by measuring glucose uptake and lactate production using commercial kits. The targeting relationship between miR-656-3p and circ-PAPPA or GNG5 was verified by bioinformatics website starBase and dual luciferase reporter gene assay assays.

resultsCirc-PAPPA was upregulated in CC and was negatively correlated with benign pathological features and 5-year survival rates of CC patients. Circ-PAPPA silencing inhibited the growth and glycolysis of CC cells through upregulating miR-656-3p. GNG5, a target of miR-656-3p, could reverse the impacts of silencing circ-PAPPA on CC cells.

conclusionCirc-PAPPA may play an oncogenic role in CC by promoting cell growth and glycolysis through the miR-656-3p/GNG5 axis.

Indexed as

Colonic NeoplasmsGlycolysisMicroRNAsRNA, CircularAgedApoptosisCell Line, TumorCell MovementCell ProliferationDisease ProgressionFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedPancreatitis-Associated ProteinsMicroRNAsPancreatitis-Associated ProteinsRNA, Circularcirc-PAPPAColon cancerGlycolysisGNG5Proliferation

Identifiers

PMID39951875
PMCPMC11874721

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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.