Evidence map›Paper›PMID 31369196›Full record

ArticleMolecular oncology2019

Down-regulation of long noncoding RNA PVT1 inhibits esophageal carcinoma cell migration and invasion and promotes cell apoptosis via microRNA-145-mediated inhibition of FSCN1.

Si-Ning Shen, Ke Li, Ying Liu, Cheng-Liang Yang, Chun-Yu He, Hao-Rang Wang

RetractedOpen access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.1field-weighted citation impact, top 4% 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

45 citing papers in PubMed, 71 citations in OpenAlex.

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  9. lncRNA PVT1: a novel oncogene in multiple cancers.Cellular & molecular biology letters · 2022
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4 · The record

Corrections and comments

  • Retraction · 2022-12-02Concerns/Issues about Image · Original Data and/or Images not Provided and/or not Available ·
5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Si-Ning ShenDepartment of Thoracic Surgery, Affiliated Cancer Hospital of Zhengzhou University (Henan Cancer Hospital), China.ORCID 0000-0001-9573-4426
Ke LiDepartment of Oncology, Affiliated Cancer Hospital of Zhengzhou University (Henan Cancer Hospital), China.
Ying LiuDepartment of Oncology, Affiliated Cancer Hospital of Zhengzhou University (Henan Cancer Hospital), China.
Cheng-Liang YangDepartment of Radiation Oncology, Affiliated Cancer Hospital of Zhengzhou University (Henan Cancer Hospital), China.
Chun-Yu HeDepartment of Radiation Oncology, Affiliated Cancer Hospital of Zhengzhou University (Henan Cancer Hospital), China.
Hao-Rang WangDepartment of Thoracic Surgery, Affiliated Cancer Hospital of Zhengzhou University (Henan Cancer Hospital), China.
Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulating evidence has established that long noncoding RNA (lncRNA) plasmacytoma variant translocation 1 (PVT1) is a tumor regulator in many cancers. Here, we aimed to investigate the possible function of lncRNA PVT1 in esophageal carcinoma (EC) via targeting of microRNA-145 (miR-145). Initially, microarray-based gene expression profiling of EC was employed to identify differentially expressed genes. Moreover, the expression of lncRNA PVT1 was examined and the cell line presenting with the highest level of lncRNA PVT1 expression was selected for subsequent experiments. We then proceeded to examine interaction among lncRNA PVT1, FSCN1, and miR-145. The effect of lncRNA PVT1 on viability, migration, invasion, apoptosis, and tumorigenesis of transfected cells was examined with gain-of-function and loss-of-function experiments. We observed that lncRNA PVT1 was robustly induced in EC. lncRNA PVT1 could bind to miR-145 and regulate its expression, and FSCN1 is a target gene of miR-145. Overexpression of miR-145 or silencing of lncRNA PVT1 was revealed to suppress cell viability, migration, and invasion abilities, while also stimulating cell apoptosis. Furthermore, our in vivo results showed that overexpression of miR-145 or silencing of lncRNA PVT1 resulted in decreased tumor growth in nude mice. In conclusion, our research reveals that down-regulation of lncRNA PVT1 could potentially promote expression of miR-145 to repress cell migration and invasion, and promote cell apoptosis through the inhibition of FSCN1. This highlights the potential of lncRNA PVT1 as a therapeutic target for EC treatment.

Indexed as

ApoptosisCarrier ProteinsCell MovementDown-RegulationEsophageal NeoplasmsMicrofilament ProteinsMicroRNAsNeoplasm ProteinsRNA, Long NoncodingRNA, NeoplasmAdultAgedAnimalsCell Line, TumorFemaleGene Expression Regulation, NeoplasticCarrier ProteinsFSCN1 protein, humanMicrofilament ProteinsMicroRNAsMIRN145 microRNA, humanNeoplasm ProteinsPVT1 long-non-coding RNA, humanRNA, Long NoncodingRNA, Neoplasmapoptosisesophageal carcinomaFSCN1long noncoding RNAmicroRNA-145plasmacytoma variant translocation 1

Identifiers

PMID31369196
PMCPMC6887590
OpenAlexW2965695059

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Registered trials

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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.