Evidence map›Paper›PMID 32418155›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2020

LncRNA DCST1-AS1 downregulates miR-29b through methylation in glioblastoma (GBM) to promote cancer cell proliferation.

S Hu, Y Yao, X Hu, Y Zhu

Abstract read
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In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 30% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

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  7. LncRNA-mediated DNA methylation: an emerging mechanism in cancer and beyond.Journal of experimental & clinical cancer research : CR · 2022
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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

4 authors at 1 institution in 1 country.

S HuDepartment of NeurosurgeryHuangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, Huangshi City, 435000, Hubei Province, People's Republic of China.
Y YaoDepartment of NeurosurgeryHuangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, Huangshi City, 435000, Hubei Province, People's Republic of China.
X HuDepartment of NeurosurgeryHuangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, Huangshi City, 435000, Hubei Province, People's Republic of China.
Y ZhuDepartment of Rehabilitation, Huangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, No. 141 Tianjin Road, Huangshi Gang District, Huangshi City, 435000, Hubei Province, People's Republic of China. dk6079@163.com.ORCID http://orcid.org/0000-0002-5198-5941
Hubei Polytechnic University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe role of DCST1-AS1 has been investigated in several types of cancer, while the role of DCST1-AS1 in glioblastoma (GBM) is unclear. This study aimed to investigate the role of DCST1-AS1 in GBM.

methodsGBM and paired non-tumor tissues were collected from 62 GBM patients. Expression levels of DCST1-AS1 and miR-29b in paired tissue samples were determined by RT-qPCR. The role of DCST1-AS1 in regulating the methylation of miR-29b was assessed by methylation-specific PCR (MSP). Cell proliferation was analyzed by cell proliferation assay.

resultsIt was observed that the upregulation of DCST1-AS1 in GBM predicted poor survival. MiR-29b was downregulated in GBM and inversely correlated with the expression of DCST1-AS1. In GBM cells, overexpression of DCST1-AS1 resulted in the downregulation of miR-29b and the increased methylation level of miR-29b gene. Overexpression of DCST1-AS1 resulted in increased cell proliferation. Moreover, Overexpression of DCST1-AS1 significantly reversed the inhibitory effects of miR-29b on cancer cell proliferation.

conclusionDCST1-AS1 may downregulate miR-29b through methylation in GBM to promote cancer cell proliferation.

Indexed as

AgedBrain NeoplasmsCell Line, TumorCell ProliferationDNA MethylationDown-RegulationFemaleGlioblastomaHumansMaleMicroRNAsMiddle AgedPrognosisRNA, Long NoncodingTransfectionUbiquitin-Protein LigasesDCST1 protein, humanMicroRNAsMIRN29B1 microRNA, humanRNA, Long NoncodingUbiquitin-Protein LigasesDCST1-AS1GlioblastomaMethylationmiR-29b

Identifiers

PMID32418155
OpenAlexW3025053173

What OpenQuestion holds

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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.