Evidence map›Paper›PMID 34418232›Full record

ArticleCancer science2022

Long noncoding RNA plasmacytoma variant translocation 1 promotes progression of colorectal cancer by sponging microRNA-152-3p and regulating E2F3/MAPK8 signaling.

Xin Liu, Lei Li, Jing Bai, Liang Li, Jianghe Fan, Zexian Fu, Jianxia Liu

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cancer science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Xin LiuDepartment of Medical Service, Affiliated Hospital of Hebei University of Engineering, Handan, China.
Lei LiDepartment of General Surgery, Affiliated Hospital of Hebei University of Engineering, Handan, China.
Jing BaiDepartment of Geriatrics, Affiliated Hospital of Hebei University of Engineering, Handan, China.
Liang LiDepartment of Gastroenterology, Cixian People's Hospital, Handan, China.
Jianghe FanDepartment of Oncology, Affiliated Hospital of Hebei University of Engineering, Handan, China.
Zexian FuDepartment of Scientific Research and Education, Affiliated Hospital of Hebei University of Engineering, Handan, China.
Jianxia LiuDepartment of Nursing, Affiliated Hospital of Hebei University of Engineering, Handan, China.ORCID https://orcid.org/0000-0002-9307-7693
Hebei University of Engineering · CN

Funding

The study was supported by Project of Handan science and Technology Bureau (No.1723208067-4)
6 · The paper itself

Abstract

The purpose of this study was to investigate the pathogenesis of colorectal cancer (CRC) and the effects of the long noncoding RNA plasmacytoma variant translocation 1 (PVT1) on CRC progression. Bioinformatics analysis verified PVT1 expression in tumor and normal tissues. Quantitative PCR and western blotting were used to measure mRNA and protein levels, respectively. The MTT, Transwell, colony formation, and in vivo assays were used to assess the effects of PVT1 on proliferation, migration, and invasion by CRC cells. Both PVT1 and microRNA (miR)-152-3p were shown to be colocalized in CRC cells using FISH assay. The target genes of miR-152-3p were predicted and verified by bioinformatics analysis, luciferase assay, and RNA pull-down assay. The ChIP assay revealed that E2F3 binds with the promoter of MAPK8. We found that PVT1 was overexpressed in CRC specimens, and its expression was higher in CRC cells than normal intestinal cells. Overexpression of PVT1 enhanced the proliferation, migration, and invasion of CRC cells, whereas PVT1 knockdown inhibited these processes. MicroRNA-152-3p was a target of PVT1, and E2F3 was a target of miR-152-3p. Rescue experiments confirmed the interaction between miR-152-3p and PVT1 and between miR-152-3p and E2F3. Luciferase and ChIP assay results confirmed that E2F3 modulates the transcriptional activation of MAPK8. Long noncoding RNA PVT1 activated E2F3 signaling by sponging miR-152-3p. The PVT1/miR-152-3p/E2F3/MAPK8 axis promoted CRC progression.

Indexed as

Up-RegulationCell Line, TumorColorectal NeoplasmsDisease ProgressionE2F3 Transcription FactorGene Expression Regulation, NeoplasticHCT116 CellsHT29 CellsHumansMaleMicroRNAsMitogen-Activated Protein Kinase 8Neoplasm InvasivenessNeoplasm TransplantationPromoter Regions, GeneticRNA, Long NoncodingE2F3 protein, humanE2F3 Transcription FactorMicroRNAsMIRN152 microRNA, humanMitogen-Activated Protein Kinase 8PVT1 long-non-coding RNA, humanRNA, Long Noncodingcolorectal cancerE2F3lncRNA PVT1miR-152-3p

Identifiers

PMID34418232
PMCPMC8748219
OpenAlexW3194672948

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.