Evidence map›Paper›PMID 26748613›Full record

ArticleIranian biomedical journal2016

Suppressive Effect of Constructed shRNAs against Apollon Induces Apoptosis and Growth Inhibition in the HeLa Cell Line.

Saeideh Milani, Mojgan Bandehpour, Zohreh Sharifi, Bahram Kazemi

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In one paragraph

Article in Iranian biomedical journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 37% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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.

Saeideh MilaniDepartment of Biotechnology, School of Medicine, Shahid Beheshti University of Medical Sciences, Ewin, Chamran highway, Tehran, Iran.
Mojgan BandehpourDepartment of Biotechnology, School of Medicine, Shahid Beheshti University of Medical Sciences, Ewin, Chamran highway, Tehran, Iran.
Zohreh SharifiBlood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Hemmat EXP., Tehran, Iran.
Bahram KazemiDepartment of Biotechnology, School of Medicine, Shahid Beheshti University of Medical Sciences, Ewin, Chamran highway, Tehran, Iran.
Shahid Beheshti University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCervical cancer is the second most common female cancer worldwide. Inhibitors of apoptosis proteins (IAPs) block apoptosis; therefore, therapeutic strategies targeting IAPs have attracted the interest of researchers in recent years. Apollon, a member of IAPs, inhibits apoptosis and cell death. RNA interference is a pathway in which small interfering RNA (siRNA) or shRNA (short hairpin RNA) inactivates the expression of target genes. The purpose of this study was to determine the effect of constructed shRNAs on apoptosis and growth inhibition through the suppression of apollon mRNA in HeLa cell line.

methodsThree shRNAs with binding ability to three different target sites of the first region of apollon gene were designed and cloned in pRNAin-H1.2/Neo vector. shRNA plasmids were then transfected in HeLa cells using electroporation. Down-regulation effects of apollon and the viability of HeLa cells were analyzed by RT-PCR, lactate dehydrogenase assay, and MTT assay, respectively. Also, the induction and morphological markers of apoptosis were evaluated by caspase assay and immunocytochemistry method.

resultsThe expression of shRNA in HeLa cells caused a significant decrease in the level of apollon mRNA1. In addition, shRNA1 effectively increased the mRNA level of Smac (as the antagonist of apollon), reduced the viability of HeLa cells and exhibited immunocytochemical apoptotic markers in this cell line.

conclusionApollon gene silencing can induce apoptosis and growth impairment in HeLa cells. In this regard, apollon can be considered a candidate therapeutic target in HeLa cells as a positive human papillomavirus cancer cell line.

Indexed as

ApoptosisApoptosis Regulatory ProteinsCell Line, TumorCell ProliferationCell SurvivalFemaleHeLa CellsHumansInhibitor of Apoptosis ProteinsIntracellular Signaling Peptides and ProteinsMitochondrial ProteinsRNA, MessengerRNA, Small InterferingUterine Cervical NeoplasmsApoptosis Regulatory ProteinsBIRC6 protein, humanDIABLO protein, humanInhibitor of Apoptosis ProteinsIntracellular Signaling Peptides and ProteinsMitochondrial ProteinsRNA, MessengerRNA, Small InterferingCoronary artery diseaseGenetic association studyIranSingle nucleotide polymorphisms

Identifiers

PMID26748613
PMCPMC4949978
OpenAlexW2259797146

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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.