Evidence map›Paper›PMID 23840656›Full record

ArticlePloS one2013

Anti-Proliferative Effects of Evodiamine on Human Breast Cancer Cells.

Kai-Lee Wang, Shih-Min Hsia, Jiun-Yih Yeh, Shao-Chi Cheng, Paulus S Wang, Shyi-Wu Wang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  5. Review
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  8. Research progress on evodiamine, a bioactive alkaloid ofExperimental and therapeutic medicine · 2021
    Review
  9. Article
  10. Antiproliferative Effects of Alkaloid Evodiamine and Its Derivatives.International journal of molecular sciences · 2018
    Review
  11. Article
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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

6 authors at 3 institutions in 1 country.

Kai-Lee WangDepartment of Physiology, School of Medicine, National Yang-Ming University, Taipei, Taiwan, Republic of China ; The Center of General Education, National Taipei University of Nursing and Health Sciences, Taipei, Taiwan, Republic of China.
Shih-Min Hsia
Jiun-Yih Yeh
Shao-Chi Cheng
Paulus S Wang
Shyi-Wu Wang
National Yang Ming Chiao Tung University · TWChang Gung University · TWTaipei Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endocrine sensitivity, assessed by the expression of estrogen receptor (ER), has long been the predict factor to guide therapeutic decisions. Tamoxifen has been the most successful hormonal treatment in endocrine-sensitive breast cancer. However, in estrogen-insensitive cancer tamoxifen showed less effectiveness than in estrogen-sensitive cancer. It is interesting to develop new drugs against both hormone-sensitive and insensitive tumor. In this present study we examined anticancer effects of evodiamine extracted from the Chinese herb, Evodiae fructus, in estrogen-dependent and -independent human breast cancer cells, MCF-7 and MDA-MB-231 cells, respectively. Evodiamine inhibited the proliferation of MCF-7 and MDA-MB-231 cells in a concentration-dependent manner with concentration of 1×10(-6) and 1×10(-5) M. Evodiamine also induced apoptosis via up-regulation of caspase 7 activation, PARP cleavage (Bik and Bax expression). The expression of ER α and β in protein and mRNA levels was down-regulated by evodiamine according to data from immunoblotting and RT-PCR analysis. Overall, our results indicate that evodiamine mediates degradation of ER and induces caspase-dependent pathway leading to inhibit proliferation of breast cancer cell lines. It suggests that evodiamine may in part mediate through ER-inhibitory pathway to inhibit breast cancer cell proliferation.

Indexed as

Antineoplastic Agentsbcl-2-Associated X ProteinBreast NeoplasmsCaspase 7Cell ProliferationDose-Response Relationship, DrugEstradiolEstrogen Receptor alphaEstrogen Receptor betaEstrogensFulvestrantGene Expression Regulation, NeoplasticHumansMCF-7 CellsQuinazolinesAntineoplastic Agentsbcl-2-Associated X ProteinCaspase 7EstradiolEstrogen Receptor alphaEstrogen Receptor betaEstrogensevodiamineFulvestrantQuinazolines

Identifiers

PMID23840656
PMCPMC3694052
OpenAlexW1978072703

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.