Evidence map›Paper›PMID 28974748›Full record

ArticleScientific reports2017

Cytological Assessments and Transcriptome Profiling Demonstrate that Evodiamine Inhibits Growth and Induces Apoptosis in a Renal Carcinoma Cell Line.

Xiao-Long Yuan, Peng Zhang, Xin-Min Liu, Yong-Mei Du, Xiao-Dong Hou, Sen Cheng, Zhong-Feng Zhang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. 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
2.2field-weighted citation impact, top 12% 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, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Consumption of Wild Rice (International journal of molecular sciences · 2020
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Antifungal Prenylated Diphenyl Ethers fromMolecules (Basel, Switzerland) · 2018
    Article
  10. Article
  11. Antiproliferative Effects of Alkaloid Evodiamine and Its Derivatives.International journal of molecular sciences · 2018
    Review
  12. Article
  13. Ethanol Extract ofNutrients · 2018
    Article
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

7 authors at 2 institutions in 1 country.

Xiao-Long YuanTobacco Research Institute of Chinese Academy of Agricultural Sciences, Qingdao, China.
Peng ZhangTobacco Research Institute of Chinese Academy of Agricultural Sciences, Qingdao, China.
Xin-Min LiuTobacco Research Institute of Chinese Academy of Agricultural Sciences, Qingdao, China.
Yong-Mei DuTobacco Research Institute of Chinese Academy of Agricultural Sciences, Qingdao, China.
Xiao-Dong HouTobacco Research Institute of Chinese Academy of Agricultural Sciences, Qingdao, China.
Sen ChengShanghai Tobacco Group Company Limited, Shanghai, China.
Zhong-Feng ZhangTobacco Research Institute of Chinese Academy of Agricultural Sciences, Qingdao, China. zhangzhongfeng@caas.cn.
Tobacco Research Institute · CNChinese Academy of Agricultural Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chinese medicines are an important source of secondary metabolites with excellent antitumour activity. Evodia rutaecarpa, from the family Rutaceae, exhibits antitumour activity. Evodiamine (EVO), which was isolated from the fruit of E. rutaecarpa, exhibits robust antitumour activity. However, the antitumour mechanism of EVO remains unclear. In this study, we assessed the growth-inhibiting effect of EVO on two renal carcinoma cell lines. We found that EVO could change the morphology and decrease the viability and proliferation of cells in a time- and concentration-dependent manner in vitro. In addition, transcriptome analysis indicated that EVO can modulate the transcriptome of Caki-1 cells. In total, 7,243 differentially expressed genes were found, among which 3,347 downregulated genes and 3,896 upregulated genes were mainly involved in cell migration, apoptosis, cell cycle, and DNA replication. Furthermore, we demonstrated that EVO can cause apoptosis, arrest cells in the G2/M phase, and regulate the expression of apoptosis- and cell cycle-related genes in Caki-1 cells. Our study reveals the anticancer effects of EVO using cellular and molecular data, and indicates the potential uses of this compound as a resource to characterize the antitumour mechanisms of E. rutaecarpa.

Indexed as

Antineoplastic Agents, PhytogenicApoptosisCarcinoma, Renal CellCell Line, TumorCell MovementCell ProliferationGene Expression ProfilingGene Expression Regulation, NeoplasticHumansNeoplasm ProteinsQuinazolinesSignal TransductionTranscriptomeAntineoplastic Agents, PhytogenicevodiamineNeoplasm ProteinsQuinazolines

Identifiers

PMID28974748
PMCPMC5626725
OpenAlexW2759206384

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.