Evidence map›Paper›PMID 36344947›Full record

ArticleBMC cancer2022

LncRNA MEG3 promotes cisplatin sensitivity of cervical cancer cells by regulating the miR-21/PTEN axis.

Ying Du, Gang Geng, Chunquan Zhao, Tian Gao, Bin Wei

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Therapy resistance-related ncRNAs in cervical cancer: biomarkers and therapeutic targets.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2026
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  19. HNRNPA2B1-mediated mJournal of translational medicine · 2023
    Article
  20. lncHUB2: aggregated and inferred knowledge about human and mouse lncRNAs.Database : the journal of biological databases and curation · 2023
    Article
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

5 authors at 1 institution in 1 country.

Ying DuDepartment of Gynecology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Gang GengDepartment of Respiratory, Children's Hospital of Chongqing Medical University, Chongqing, 400014, China.
Chunquan ZhaoDepartment of Gynecology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Tian GaoDepartment of Gynecology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Bin WeiDepartment of Dermatology, The First Affiliated Hospital of Chongqing Medical University, No. 1 Youyi Road, Yuzhong District, Chongqing, 400016, China. wb_cmu@hotmail.com.
Chongqing Medical University · CN

Funding

Chongqing Science and Technology Commission, general program 2020jcyj-msxmX0477
6 · The paper itself

Abstract

backgroundCervical cancer (CC) is a common gynecological malignancy worldwide. Some patients perform serious resistance after chemotherapy, and long-stranded non-coding RNA MEG3 is reported to be involved in the regulation of chemoresistance in many solid tumors. However, its involvement in cervical adenocarcinoma has not been reported.

methodsHela cell lines, cisplatin-resistant cell lines (Hela-CR) and nude mice were used in this study. After MEG3 was overexpressed or knocked down in cells by the lentivirus vector, cell growth was detected by the CCK-8 assay, and cell migration was evaluated using Transwell assay. Quantitative real-time polymerase chain reaction (qRT-PCR) was performed to examine the expression of MEG3, miR-21 and PTEN mRNA. Apoptosis was detected by flow cytometry. The targeting relationship between mRNAs was predicted and verified using dual-luciferase reporter gene experiments. Western blot was executed to examine Bax, cleaved-caspase 3, Bcl-2, PTEN and GAPDH expression. Cells were injected into the mice to form xenograft tumors to compare tumorigenesis capacity.

resultsWe demonstrated that MEG3 was down-regulated in cervical cancer by analyzing the TCGA database. Moreover, knockdown of MEG3 promoted CC cell proliferation, migration and inhibited the apoptosis. These changes of CC cells were more pronounced under cisplatin treatment. Further studies showed that the MEG3/miR-21/PTEN axis affected cisplatin sensitivity in cervical cancer cells, and these results of recue assay were used to confirm this conclusion.

conclusionsMEG3 performing as ceRNA promotes cisplatin sensitivity in CC cells through the miR-21/PTEN axis.

Indexed as

MicroRNAsRNA, Long NoncodingUterine Cervical NeoplasmsAnimalsCell Line, TumorCell ProliferationCisplatinFemaleGene Expression Regulation, NeoplasticHeLa CellsHumansMiceMice, NudePTEN PhosphohydrolaseRNA, MessengerCisplatinMicroRNAsMIRN21 microRNA, humanPTEN PhosphohydrolasePTEN protein, humanRNA, Long NoncodingRNA, MessengerCervical cancerCisplatin; chemosensitivityMEG3miR-21PTEN

Identifiers

PMID36344947
PMCPMC9641762
OpenAlexW4308470177

What OpenQuestion holds

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LicenceCC BY
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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.