Evidence map›Paper›PMID 26876254›Full record

ArticleZhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi2016

[Promoter methylation status of SFRP genes and induced apoptosis by demethylation in Jurkat cells].

Chengbo Xu, Jianzhen Shen, Bin Liao, Haiying Fu, Huarong Zhou, Yan Qi, Zhenping Huangfu, Yining Chen, Jiawei Chen

Open access · greenAbstract read
In one paragraph

Article in Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Chengbo XuDepartment of Hematology, the Affiliated People's Hospital of Fujian University of Traditional Chinese Medicine, Fuzhou 350004, China.
Jianzhen Shen
Bin Liao
Haiying Fu
Huarong Zhou
Yan Qi
Zhenping Huangfu
Yining Chen
Jiawei Chen
Fujian University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo study the promoter methylation status of SFRP genes and the effect of 5- aza- 2'- deoxycytidine (5- Aza- CdR)induced apoptosis via Wnt/β- catenin pathway by demethylation in Jurkat cells.

methodsJurkat cells were treated with different concentrations of 5- Aza- CdR. The cell proliferation level of Jurkat cells was detected by MTT assay. Apoptosis was evaluated by flow cytometry. Methylation- spcific PCR (MSP) was used to determine the methylation status of SFRP genes. The expressions of SFRP genes were detected by real time fluorescence quantitative PCR. The mRNA expression levels of survivin, c- myc and cyclin- D1 were analyzed by RT- PCR. Western blot was used to detect the levels of β-catenin protein.

resultsCompared with control group, the different concentrations of 5-Aza-CdR could significantly inhibit the proliferation of Jurkat cells in a time-dose dependent manner (P<0.05). After being treated by 5- Aza- CdR for 48 hours, the cell early apoptosis rate in experiment group was significantly higher than that in control group (P<0.05). The promoters of SFRP1, SFRP2, SFRP4, SFRP5 genes were hypermethylation state in the control group, after being treated by 5-Aza-CdR for 72 hours, the brightness of SFRP1, SFRP2, SFRP4, SFRP5 genes' methylation strips weakened in a dose- dependent manner. SFRP mRNA expression increased (P<0.05) when 5- Aza- CdR concentration increased, and the level of β- catenin protein was dampened in a dose- dependent manner (P<0.05). As compared to the control group, the mRNA expressions of associated apoptosis genes survivin, c-myc and cyclin- D1, respectively were obviously down- regulated in a dose- dependent manner (P<0.05).

conclusionThe effect of demethylation could up- regulate SFRP genes expressions by reversing its hypermethylation and induced apoptosis by down-regulation of β-catenin and associated apoptosis genes.

Indexed as

DNA MethylationPromoter Regions, GeneticWnt Signaling PathwayApoptosisAzacitidinebeta CateninCell ProliferationDecitabineDown-RegulationGene ExpressionHumansIntercellular Signaling Peptides and ProteinsJurkat CellsMembrane ProteinsSecreted Frizzled-Related ProteinsAzacitidinebeta CateninCTNNB1 protein, humanDecitabineIntercellular Signaling Peptides and ProteinsMembrane ProteinsSecreted Frizzled-Related ProteinsSFRP1 protein, human

Identifiers

PMID26876254
PMCPMC7342293
OpenAlexW2279271169

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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.