Evidence map›Paper›PMID 30697971›Full record

ArticleJournal of cellular and molecular medicine2019

LncRNA LINC01305 silencing inhibits cell epithelial-mesenchymal transition in cervical cancer by inhibiting TNXB-mediated PI3K/Akt signalling pathway.

Shu-Ping Yan, Dan-Xia Chu, Hai-Feng Qiu, Ya Xie, Chun-Fang Wang, Jian-Ying Zhang, Wen-Cai Li, Rui-Xia Guo

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Journal of cellular and molecular medicine, 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 It has been retracted, and should not be counted.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 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 36 citations in OpenAlex.

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  14. Intelligent Diagnosis of Cervical Cancer Based on Data Mining Algorithm.Computational and mathematical methods in medicine · 2021
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4 · The record

Corrections and comments

  • Retraction · 2021-10-01Duplication of/in Image · Investigation by Journal/Publisher · Objections by Third Party · Paper Mill · · see also: https://pubpeer.com/publications/530CE9B31AC88A0FD46DFB4A12B8F1;
  • Retracted
5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Shu-Ping YanDepartment of Pathology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, P.R. China.
Dan-Xia ChuDepartment of Gynecology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, P.R. China.
Hai-Feng QiuDepartment of Gynecology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, P.R. China.
Ya XieDepartment of Gynecology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, P.R. China.
Chun-Fang WangDepartment of Gynecology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, P.R. China.
Jian-Ying ZhangInstitute of Medical and Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, Henan Province, P.R. China.
Wen-Cai LiDepartment of Pathology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, P.R. China.
Rui-Xia GuoDepartment of Gynecology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, P.R. China.ORCID 0000-0002-8847-2488
First Affiliated Hospital of Zhengzhou University · CNZhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical cancer (CC) remains one of the leading malignancies afflicting females worldwide, with its aetiology associated with long-term papillomavirus infection. Recent studies have shifted their focus and research attention to the relationship between long non-coding RNAs (lncRNAs) and CC therapeutic. Thus, the aim of the current study was to investigate the underlying mechanism of lncRNA LINC01305 on the cell invasion, migration and epithelial-mesenchymal transition (EMT) of CC cells via modulation of the PI3K/Akt signalling pathway by targeting tenascin-X B (TNXB). The expressions of LINC01305, TNXB, MMP2, MMP9, E-cadherin, vimentin, PI3K, Akt, p-PI3K, p-Akt and TNXB were detected in this study. After which, the cell invasion and migration abilities of the CC cells were determined respectively. Bioinformatics and the application of a dual luciferase reporter gene assay provided verification indicating that TNXB is the target gene of lncRNA LINC01305. Reverse transcription quantitative polymerase chain reaction (RT-qPCR) and western blot analysis methods revealed that the expressions of MMP2, MMP9, vimentin, PI3K, Akt, p-PI3K and p-Akt were decreased following the down-regulation of LncRNA LINC01305 or overexpression of TNXB. LncRNA LINC01305 silencing or TNXB overexpression was noted to decrease the migration and invasion of SiHa cells. Taken together, the key findings of the current study present evidence suggesting that lncRNA LINC01305 silencing suppresses EMT, invasion and migration via repressing the PI3K/Akt signalling pathway by means of targeting TNXB in CC cells, which ultimately provides novel insight and identification of potential therapeutic targets for CC.

Indexed as

Gene Expression Regulation, NeoplasticAntigens, CDApoptosisCadherinsCell Line, TumorCell MovementCell ProliferationComputational BiologyEpithelial-Mesenchymal TransitionFemaleHeLa CellsHumansMatrix Metalloproteinase 2Matrix Metalloproteinase 9Phosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktAntigens, CDCadherinsCDH1 protein, humanMatrix Metalloproteinase 2Matrix Metalloproteinase 9MMP2 protein, humanMMP9 protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRNA, Long NoncodingRNA, Small InterferingTenascintenascin XVimentinVIM protein, humancervical cancerepithelial-mesenchymal transitioninvasionlong non-coding RNA LINC01305migrationPI3K/Akt signalling pathwayTNXB

Identifiers

PMID30697971
PMCPMC6433725
OpenAlexW2913585446

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.