Evidence map›Paper›PMID 29132471›Full record

ArticleZhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics2017

[Oridonin inhibits proliferation of Jurkat cells via the down-regulation of Brg1].

Zhen-Zhen Ye, Fei-Long Xue, Wen-Ping Ding, Xiang Kong, Yi-Na Shen

Open access · greenAbstract read
In one paragraph

Article in Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, 2017. 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
0.1field-weighted citation impact, top 46% 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. The Role of BRG1 in Antioxidant and Redox Signaling.Oxidative medicine and cellular longevity · 2020
    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

5 authors at 1 institution in 1 country.

Zhen-Zhen YeDepartment of Pediatrics, Yijishan Hospital, Wannan Medical College, Wuhu, Anhui 241001, China. synsyn5252@sina.com.
Fei-Long Xue
Wen-Ping Ding
Xiang Kong
Yi-Na Shen
Wannan Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the effect of oridonin on the human acute lymphocytic leukemia cell line Jurkat and its mechanism.

methodsJurkat cells were cultured in vitro and treated with various concentrations (0, 1.25, 2.5, 5, and 10 μmol/L) of oridonin for different lengths of time (24, 48, and 72 hours). The proliferation of Jurkat cells was analyzed by MTT assay. The changes in nuclear morphology were evaluated by fluorescence microscopy at 12 hours after treatment with various concentrations of oridonin. The expression levels of Brg1, P53, and C-myc were determined by semi-quantitative Western blot in Jurkat cells treated with various concentrations of oridonin for 24 hours or 5 μmol/L oridonin for various lengths of time (0, 2, 6, 12, and 24 hours). The expression levels of P53 and C-myc and proliferation of Jurkat cells were evaluated after Brg1 expression was knocked down by Brg1-specific siRNA.

resultsCompared with the control group, the proliferation of oridonin-treated Jurkat cells was significantly inhibited in a concentration- and time-dependent manner (P<0.05). According to the florescence microscopic analysis, oridonin treatment led to nuclear pyknosis in Jurkat cells. Compared with the control group, Jurkat cells treated with 5 μmol/L oridonin had reduced expression of Brg1 and C-myc but elevated expression of P53. Brg1 knock-down led to a significant reduction in proliferation of Jurkat cells (P<0.05), up-regulated expression of P53, and down-regulated expression of C-myc.

conclusionsOridonin can inhibit the proliferation of Jurkat cells, probably via the Brg1 signaling pathway.

Indexed as

Antineoplastic Agents, PhytogenicCell ProliferationDiterpenes, KauraneDNA HelicasesDose-Response Relationship, DrugDown-RegulationHumansJurkat CellsNuclear ProteinsPrecursor Cell Lymphoblastic Leukemia-LymphomaProto-Oncogene Proteins c-mycSignal TransductionTranscription FactorsTumor Suppressor Protein p53Antineoplastic Agents, PhytogenicDiterpenes, KauraneDNA HelicasesMYC protein, humanNuclear ProteinsoridoninProto-Oncogene Proteins c-mycSMARCA4 protein, humanTranscription FactorsTumor Suppressor Protein p53

Identifiers

PMID29132471
PMCPMC7389326
OpenAlexW3012234454

What OpenQuestion holds

Textmetadata
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.