Evidence map›Paper›PMID 24633222›Full record

ArticlePloS one2014

Hepatitis B virus induces cell proliferation via HBx-induced microRNA-21 in hepatocellular carcinoma by targeting programmed cell death protein4 (PDCD4) and phosphatase and tensin homologue (PTEN).

Preeti Damania, Bijoya Sen, Sadaf Bashir Dar, Satendra Kumar, Anupama Kumari, Ekta Gupta, Shiv Kumar Sarin, Senthil Kumar Venugopal

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.5field-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

48 citing papers in PubMed, 89 citations in OpenAlex.

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  14. Cell death pathways and viruses: Role of microRNAs.Molecular therapy. Nucleic acids · 2021
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  18. [Pregnane X receptor promotes programmed cell death protein 4 expression in HepG2 cells].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2020
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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

8 authors at 2 institutions in 1 country.

Preeti DamaniaInstitute of Liver and Biliary Sciences, New Delhi, India.
Bijoya SenInstitute of Liver and Biliary Sciences, New Delhi, India.
Sadaf Bashir DarInstitute of Liver and Biliary Sciences, New Delhi, India.
Satendra KumarSouth Asian University, New Delhi, India.
Anupama KumariInstitute of Liver and Biliary Sciences, New Delhi, India.
Ekta GuptaInstitute of Liver and Biliary Sciences, New Delhi, India.
Shiv Kumar SarinInstitute of Liver and Biliary Sciences, New Delhi, India.
Senthil Kumar VenugopalSouth Asian University, New Delhi, India.
Institute of Liver and Biliary Sciences · INSouth Asian University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatitis B viral infection-induced hepatocellular carcinoma is one of the major problems in the developing countries. One of the HBV proteins, HBx, modulates the host cell machinery via several mechanisms. In this study we hypothesized that HBV enhances cell proliferation via HBx-induced microRNA-21 in hepatocellular carcinoma. HBx gene was over-expressed, and miRNA-21 expression and cell proliferation were measured in Huh 7 and Hep G2 cells. miRNA-21 was over-expressed in these cells, cell proliferation and the target proteins were analyzed. To confirm the role of miRNA-21 in HBx-induced proliferation, Hep G 2.2.1.5 cells (a cell line that expresses HBV stably) were used for miRNA-21 inhibition studies. HBx over-expression enhanced proliferation (3.7- and 4.5-fold increase; n = 3; p<0.01) and miRNA-21 expression (24- and 36-fold increase, normalized with 5S rRNA; p<0.001) in Huh 7 and Hep G2 cells respectively. HBx also resulted in the inhibition of miRNA-21 target proteins, PDCD4 and PTEN. miRNA-21 resulted in a significant increase in proliferation (2- and 2.3-fold increase over control cells; p<0.05 in Huh 7 and Hep G2 cells respectively) and decreased target proteins, PDCD4 and PTEN expression. Anti-miR-21 resulted in a significant decrease in proliferation (p<0.05) and increased miRNA-21 target protein expression. We conclude that HBV infection enhances cell proliferation, at least in part, via HBx-induced miRNA-21 expression during hepatocellular carcinoma progression.

Indexed as

Apoptosis Regulatory ProteinsCarcinoma, HepatocellularCell Line, TumorCell ProliferationGene ExpressionHepatitis B virusHumansLiver NeoplasmsMicroRNAsPTEN PhosphohydrolaseRNA-Binding ProteinsRNA InterferenceTrans-ActivatorsTransfectionViral Regulatory and Accessory ProteinsApoptosis Regulatory Proteinshepatitis B virus X proteinMicroRNAsMIRN21 microRNA, humanPDCD4 protein, humanPTEN PhosphohydrolaseRNA-Binding ProteinsTrans-ActivatorsViral Regulatory and Accessory Proteins

Identifiers

PMID24633222
PMCPMC3954734
OpenAlexW2081803884

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.