Evidence map›Paper›PMID 25482936›Full record

ArticleCancer biology & therapy2015

Cryptotanshinone inhibits breast cancer cell growth by suppressing estrogen receptor signaling.

Shanhu Li, Hongtao Wang, Liu Hong, Wei Liu, Fang Huang, Jian Wang, Peng Wang, Xiaoqing Zhang, Jianguang Zhou

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
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  5. Review
  6. Article
  7. Frontiers in pharmacology · 2022
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Perspectives on the Clinical Development of NRF2-Targeting Drugs.Handbook of experimental pharmacology · 2021
    Review
  14. Article
  15. Article
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  17. 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

9 authors at 6 institutions in 3 countries.

Shanhu Lia Laboratory of Medical Molecular Biology; Beijing Institute of Biotechnology ; Beijing , PR China.
Hongtao Wang
Liu Hong
Wei Liu
Fang Huang
Jian Wang
Peng Wang
Xiaoqing Zhang
Jianguang Zhou
Beijing Administration Institute · CNMRC Laboratory of Molecular Biology · GBCzech Academy of Sciences, Institute of Biotechnology · CZGuiyang University · CNPeking Union Medical College Hospital · CNTianjin Institute of Pharmaceutical Research (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Estrogen receptor (ER) is a major therapeutic target for the treatment of breast cancer, because of the crucial role of estrogen signaling deregulation in the development and progression of breast cancer. In this study, we report the identification of a novel ERα binding compound, cryptotanshinone (CPT), by screening the CADD database. We also show that CPT effectively inhibits estrogen-induced ER transactivation and gene expression of ER target genes. Furthermore, we showed that CPT suppressed breast cancer cell growth mainly in an ERα dependent manner. Finally, we confirmed the potential therapeutic efficiency of CPT using xenograft experiments in vivo. Taken together, our results describe a novel mechanism for the anticancer activity of CPT and provide supporting evidence for its use as a potential therapeutic agent to treat patients with ERα positive breast cancer.

Indexed as

AnimalsBreast NeoplasmsCell Line, TumorCell ProliferationCell SurvivalDisease Models, AnimalEstrogen Receptor alphaFemaleGene Expression Regulation, NeoplasticHumansMiceModels, MolecularMolecular Docking SimulationPhenanthrenesProtein ConformationReceptors, EstrogencryptotanshinoneEstrogen Receptor alphaPhenanthrenesReceptors, Estrogenbreast cancerCADD, computer-aided drug designCPT, cryptotanshinonecryptotanshinoneEREs, estrogen-responsive elementsER, estrogen receptorestradiolestrogen receptorROS, reactive oxygen speciesSERM, selective estrogen receptor modulator

Identifiers

PMID25482936
PMCPMC4622426
OpenAlexW2047868617

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.